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The Journal of Neuroscience, December 1, 2002, 22(23):10333-10345

Histone Deacetylase Activity Is Necessary for Oligodendrocyte Lineage Progression

Mireya Marin-Husstege, Michela Muggironi, Aixiao Liu, and Patricia Casaccia-Bonnefil

Department of Neuroscience and Cell Biology, University of Medicine and Dentistry of New Jersey, R. Wood Johnson Medical School, Piscataway, New Jersey 08854


    ABSTRACT

TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Gene expression can be modulated by chromatin changes induced by histone acetylation and deacetylation. Acetylation of histone lysine residues by acetyltransferases is associated with transcriptionally active chromatin, whereas the removal of acetyl groups by histone deacetylases (HDACs) correlates with repressed chromatin. Recent evidence has shown that histone deacetylation is responsible for restricting neuronal gene expression, whereas histone acetylation is necessary for astrocytic differentiation We now asked whether histone acetylation or deacetylation was necessary for oligodendrocyte differentiation. Neonatal rat cortical progenitors were kept proliferating and undifferentiated in the presence of mitogens and induced to stop proliferating and differentiate into oligodendrocytes by mitogen removal. Histone deacetylation was observed during the temporal window between exit from the cell cycle and onset of differentiation, which was characterized by acquisition of branched morphology and myelin gene expression. Blocking HDAC activity during this critical window using the inhibitor trichostatin A (TSA) prevented the progression of progenitors into mature oligodendrocytes. TSA-treated progenitors were able to exit from the cell cycle but did not progress to oligodendrocytes. Their development was arrested at the progenitor stage, characterized by simple morphology and lack of myelin gene expression. The effect of TSA on progenitor differentiation was lineage specific, because TSA did not affect the ability of these cells to differentiate into type II astrocytes when cultured in the presence of serum. From these data, we conclude that histone deacetylation is a necessary component of the oligodendrocyte differentiation program.

Key words: myelin; differentiation; transcription; trichostatin A; chromatin; development


    INTRODUCTION

TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

The complexity of the mammalian brain results from the activation of genetic differentiation programs leading to three distinct cell types: neurons, astrocytes, and oligodendrocytes. Our laboratory has been interested in defining the mechanisms responsible for oligodendrocyte differentiation and their relationship to cell cycle exit. Several studies have shown that progenitors remain undifferentiated when cultured in the presence of mitogens and differentiate into oligodendrocytes in response to mitogen withdrawal (Noble and Murray, 1984; Temple and Raff, 1985; Gard and Pfeiffer, 1993; Bansal and Pfeiffer, 1997). This suggested the existence of an obligate relationship between cell cycle exit and oligodendrocyte differentiation. Furthermore, the defective differentiation observed in oligodendrocyte progenitors isolated from mice with targeted deletion of genes encoding for cell cycle inhibitors (Casaccia-Bonnefil et al., 1997; Durand et al., 1998; Zezula et al., 2001) reinforced this concept and suggested that cell cycle exit was the driving force for differentiation. This hypothesis was tested by overexpressing specific cell cycle inhibitors in proliferating progenitors (Tikoo et al., 1998; Tang et al., 1999). Although proliferation stopped by increasing the levels of cell cycle inhibitors, progenitors were unable to progress to oligodendrocytes. Together, these studies suggested that cell cycle exit was necessary, but not sufficient, to induce differentiation.

Because the proliferative state of a cell is associated with changes of chromatin components, we asked whether modification of nucleosomal histones, the basic unit of chromatin, would be a necessary element for the activation of the oligodendrocyte differentiation program. Nucleosomes are composed of a core octamer of histones called H2A, H2B, H3, and H4, and 146 base pairs of DNA are wrapped around them. The N-terminal tail of nucleosomal histones is rich in lysine residues, which are targets for acetyltransferases (HATs) and histone deacetylases (HDACs) (Csordas, 1990). Acetylation of these lysine residues represents a very efficient way to loosen the interaction between histones and DNA and is generally associated with active transcription (Ashraf and Ip, 1998; Struhl, 1998). Conversely, deacetylation of lysine residues favors compaction of chromatin, making the access of the transcriptional apparatus to nearby promoters more difficult and therefore decreasing promoter basal activity (Jeong and Stein, 1994; Roth and Allis, 1996; Svaren and Horz, 1996).

Recruitment of the histone deacetylase activity HDAC to the promoter of neuronal genes has been shown to be essential for the repression of these genes in non-neuronal cells (Chong et al., 1995; Schoenherr and Anderson, 1995). A transcriptional factor called REST is responsible for repressing the neuronal phenotype by recruiting a large complex containing the HDAC and other repressors to negative regulatory cis-elements (RE-1) in the promoter of neuronal-specific genes (Ballas et al., 2001). Decreased expression of REST in postmitotic neurons results in the disruption of these chromatin modifier complexes and allows expression of neuronal genes (Griffith et al., 2001).

Conversely, recruitment of other chromatin modifiers, such as the p300 histone acetyltransferase, has been involved in the differentiation of astrocytes or neurons from neural stem cells (Nakashima et al., 1999; Sun et al., 2001). During astrocytic differentiation, for instance, p300 is part of a complex with other transcriptional activators, and the complex is responsible for the activation of the expression of glial fibrillary protein (GFAP) (Nakashima et al., 1999). Similarly, in differentiating neurons, p300 is part of a complex with general transcription factors and neurogenins, and this complex activates the expression of neural-specific genes, such as NeuroD (Sun et al., 2001)

We now asked whether histone acetylation is also part of the mechanism responsible for the differentiation of oligodendrocyte progenitors.


    MATERIALS AND METHODS

TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Antibodies. Antibodies against histones H3, H4, H2A, and H2B were purchased from Santa Cruz Biotechnology (Santa Cruz, CA), anti-acetyl lysine and acetylated histones H3 and H4 were from Upstate Biotechnology (Lake Placid, NY), anti-HMGN1 (high-motility group N 1) and anti-HMGN2 were kindly provided by Dr. M. Bustin (Laboratory of Medicinal Chemistry, National Cancer Institute, National Institutes of Health, Bethesda, MD), anti-actin antibodies were from Sigma (St. Louis, MO), anti-GalC was from Cedar Lane (Ontario, Canada), and anti-bromodeoxyuridine (BrdU) and anti-GFAP were from Dako (Carpinteria, CA). A2B5 or O4 antibodies were generated from hybridoma cells provided by Dr. R. Bansal (University of Connecticut, Farmington, CT), whereas the antibody against proteolipid protein (PLP) was a gift from Dr. K. Nave (Max Planck Institute, Gottingen, Germany). Secondary antibodies for Western blots were obtained from Promega (Madison, WI). Secondary antibodies conjugated to fluorescein and rhodamine used for immunohistochemistry were obtained from Southern Biotechnologies (Birmingham, AL), Amersham Biosciences (Piscataway, NJ), Jackson ImmunoResearch (West Grove, PA), and Vector Laboratories (Burlingame, CA).

Cell culture. Oligodendrocyte progenitors were isolated from the cortex of postnatal day 1 rats and cultured according to McCarthy and de Vellis (1980). Cells were maintained proliferating and undifferentiated by the addition of basic FGF (bFGF) (20 ng/ml) in Sato medium (DMEM, 100 µg/ml albumin, 100 µg/ml apo-transferrin, 16 µg/ml putrescine, 0.06 ng/ml progesterone, 40 ng/ml selenium, 5 µg/ml insulin, 1 mM sodium pyruvate, 2 mM L-glutamine, 100 U/ml penicillin, and 100 µg/ml streptomycin). The removal of bFGF from the medium (mitogen withdrawal) was considered as the start of differentiation.

Trichostatin A treatment and BrdU incorporation. Cells were cultured in the presence of bFGF and then induced to differentiate for different time intervals by removing the mitogen from the medium in the presence or absence of trichostatin A (TSA) (Sigma). Typically, TSA was used at a concentration of 10 ng/ml in all of the experiments, except for the dose-response experiment when 0.1, 1, and 10 ng/ml were tested. The effect of TSA treatment on the ability of the cell to synthesize DNA (S phase) was evaluated by labeling with 10 µM BrdU (Sigma) during the 6 hr before the end of the experiment. Labeling experiments, therefore, was started at time 0 for the 6 hr sample, at 6 hr for the 12 hr sample, at 18 hr for the 24 hr sample, and at 42 hr for the 48 hr sample. At the indicated times, cells were fixed with 4% paraformaldehyde and processed for immunocytochemistry. Cells synthesizing DNA were identified by positive immunoreactivity for BrdU as described previously (Casaccia-Bonnefil et al., 1997, 1999).

Immunoprecipitation and Western blot analysis. Whole cell lysates were prepared from proliferating progenitors (cultured in bFGF) or from differentiating cells (6, 24, and 48 hr after mitogen withdrawal). Cells were lysed in a buffer containing 50 mM HEPES, pH 7.0, 250 mM NaCl, 0.15% Nonidet P-40, 1 mM DTT, 1 mM EDTA, 0.01% PMSF, 1 mM aprotinin, and 1 mM leupeptin (Zhang et al., 2000) for 15 min on ice. Lysates were further disrupted by serial passages through syringes equipped with different sized needles (18G11/2, 22G11/2, and 26G3/8), followed by sonication on ice at the highest output (three times, 30 sec each, cells were kept on ice for 30 sec between each pulse). Equal amounts of protein (150 µg) were separated on a 15% SDS-PAGE and transferred, at 30 V for 16-18 hr, onto a 0.22 µm nitrocellulose membrane using a buffer containing 25 mM Tris base, 192 mM glycine, 20% v/v methanol, and 0.04% SDS, pH 8.3. Western blot analysis was performed as reported previously (Casaccia-Bonnefil et al., 1996, 1997, 1999) using the appropriate dilutions of primary and secondary antibodies. Equal protein loading was guaranteed by probing the blots with anti-actin antibodies. For protein immunoprecipitation experiments, equal amounts of protein (150 µg) were immunoprecipitated for 16-18 hr at 4°C using 1 µg of anti-acetyl lysine antibodies (Upstate Biotechnology). Proteins were separated by SDS-PAGE and transferred to nitrocellulose membrane, as described above, followed by Western blot analysis with antibodies against histone H3 (FL-136; Santa Cruz Biotechnology), histone H4 (H-97; Santa Cruz Biotechnology), histone H2A (H-124; Santa Cruz Biotechnology), histone H2B (FL-126; Santa Cruz Biotechnology), or antiserum against HMGN1 and HMGN2 (Dr. M. Bustin). Immunoreactive bands were visualized using HRP-conjugated secondary antibodies, followed by chemiluminescence. Typically, three to four separate experiments were conducted using cell lysates obtained from three different culture preparations. Changes in protein acetylation were evaluated by scanning the acetylated bands and the actin band with a densitometer (model 300A; Molecular Dynamics, Sunnyvale, CA) and normalizing proteins by actin content. The acetylation of the bands observed in the presence of mitogens was considered as 100%, and the values obtained for each of the other time points were described as a percentage of this value.

Reverse transcription-PCR. Total RNA was isolated using a RNeasy Mini kit (Qiagen, Hilden, Germany); 1.5 µg of total RNA was used in 40 µl of reverse transcription (RT) reaction, using a GeneAmp RT-PCR kit (Roche Products, Hertforshire, UK). The RT-PCR was performed in a 20 µl reaction mixture containing 2 µl of cDNA as template and 0.1 µM specific oligonucleotide primer pair. Cycle parameters were 30 sec at 94°C, 30 sec at 50°C, and 1.5 min at 72°C for 22 cycles. The following oligonucleotide DNA primers were used: for rat PLP, the 5' primer was 5'-GGGTTTGTTAGAGTGCTGTGCTA-3', and the 3' was 5'-CCATGAGTTTAAGGACGGCAA-3'; for rat ceramyl-galactosyl transferase (CGT) the 5' primer was 5'-GGAGTGCTGTTGGAATAGCAA-3', and the 3' was 5'-CGTACTCCTAGAACACAGACTT-3'; for rat beta -actin, the 5' primer was 5'-TGGAATCCTGTGGCATCC-3' and the 3' primer was 5'-TCGTACTCCTGCTTGCTG-3'; and for p21, the 5' primer was 5'-GTCCGATCCTGGTGATGTCCGA-3' and the 3' was 5'-GCTTTCTCTTGCAGAAGACCAA-3'.

Immunocytochemistry. Cells were grown on Permanox chambers for all immunocytochemistry. For oligodendrocyte lineage markers as A2B5, O4, and GalC, coverslips were rinsed gently with PBS (10 mM sodium phosphate, pH 7.4, and 150 mM NaCl) and incubated with hybridoma supernatant (diluted 1:1) for 30 min at 37°C. The cells were then fixed with 4% paraformaldehyde for 20 min at room temperature. For staining with antibodies against PLP or GFAP, the fixed cells were first incubated in blocking solution (0.1 M phosphate buffer, 0.1% gelatin, 1% bovine serum albumin, and 0.002% sodium azide) with 10% normal goat serum (NGS) (Vector Laboratories) and then typically incubated overnight in primary antibody diluted 1:1000. After incubation with the biotinylated secondary (1:200) for 1 hr at room temperature, immunolabeled cells were visualized using avidin conjugated with specific fluorochromes (diluted 1:500). For double immunocytochemistry with anti-BrdU antibodies, after staining, the first antibody cells were treated with 2N HCl for 10 min at room temperature, followed by neutralization in 0.1 M sodium borate, pH 8.6, for 10 min, and then they were incubated in anti-BrdU (1:100). Cells on the chamber slides were counterstained with 4',6'-diamidino-2-phenylindole (DAPI) (1:1000; Molecular Probes, Eugene, OR) to visualize cell nuclei. Labeled cells were counted in at least three fields, from two or three different experiments performed in duplicate, at 40× using an inverted fluorescence microscope (Leica, Nussloch, Germany). Cells were counted and classified according to one of the following morphologies: simple, cells are either bipolar or stellate composed exclusively of short primary branches; intermediate, defined by the presence of very long primary branches and or secondary branches; or complex morphology, defined by the presence of tertiary branches. The relative contribution of each category to the whole cell population was calculated, statistically analyzed, and represented in a graph.


    RESULTS

TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Histone deacetylation, rather than acetylation, occurs during a specific temporal window of oligodendrocyte development

To investigate whether changes in the acetylation of nucleosomal histones occurred during oligodendrocyte lineage progression, we established primary cultures of neonatal rat cortical progenitors and induced them to differentiate by removing the mitogens from the culture medium (Casaccia-Bonnefil et al., 1997). The advantage of such an experimental system is the possibility to follow in vitro the same sequence of events observed during lineage progression in vivo, although within a much shorter time frame (Noble and Murray, 1984; Temple and Raff, 1985; Gard and Pfeiffer, 1993). When cultured in the presence of mitogens, progenitors proliferate and can be identified by a simple bipolar or stellate morphology and positive immunoreactivity for the progenitor markers A2B5 and O4 (Fig. 1A). On mitogen removal, cells exit from the cell cycle within 24 hr and start acquiring secondary and tertiary branches. As progenitors mature, they lose A2B5 but retain O4 immunoreactivity. After 48-72 hr of mitogen withdrawal, differentiating oligodendrocytes begin synthesizing GalC, and, by 96-120 hr, they also express the myelin component PLP (Fig. 1A).



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  		Figure 1.   Histone deacetylation during oligodendrocyte differentiation. A, Schematic representation of oligodendrocyte lineage progression. Oligodendrocyte progenitors can be isolated from the cortex of neonatal rats and cultured in the presence of mitogens. In these conditions, cells have a simple morphology and express the A2B5 marker for early progenitors and the O4 marker for late progenitors. After removal of mitogens from the culture medium, cells exit from the cell cycle, elaborate secondary and tertiary branches, and, between 48 and 72 hr, begin synthesis of GalC, the major lipid constituent of myelin. After 96 hr from the removal of mitogens, cells express high levels of the protein constituent of myelin, PLP. B, Time course of protein deacetylation during oligodendrocyte development. Protein lysates were obtained from proliferating progenitors cultured in the presence of bFGF (0), from cells cultured for 6 (6), 24 (24), or 48 (48) hr in the absence of bFGF, and from cells treated for 24 hr with 10 ng/ml TSA in medium without bFGF. After SDS-PAGE and transfer onto nitrocellulose, the blots were probed with antibodies anti-acetyl lysine, and the bands were visualized by chemiluminescence. The size of the molecular weight markers is indicated on the left. The intensity of the chemiluminescent signal reflects the acetylation level. Reprobing the blots with anti-actin antibodies was used as loading control. C, Densitometric analysis of histone acetylation. Western blot analysis was performed as described in B using four different cellular preparations. The results of the four experiments were then scanned with a densitometer, quantitated, normalized, and represented as a bar graph. Briefly, the intensity of the signal of each band was measured and normalized by the actin content. The signal of the band detected in progenitors cultured in bFGF was arbitrarily chosen as 100% value, and the acetylation of each sample was referred to as a percentage of that value.

To detect changes in histone acetylation during oligodendrocyte lineage progression, protein extracts were harvested from proliferating progenitors cultured in bFGF after 6, 24, and 48 hr of mitogen withdrawal and analyzed by Western blot analysis using an antibody directed against acetyl-lysine residues. Interestingly, two heavily acetylated bands ranging between 10 and 17 kDa were present in proliferating progenitors (Fig. 1B). As early as 6 hr after mitogen withdrawal, the intensity of the signal for both bands decreased, indicating loss of the acetyl groups from the lysine residues. The decrease of intensity was observed throughout the duration of the experiment, with the weakest acetylation signal observed in cells cultured for 24 hr after mitogen withdrawal (Fig. 1B). Treatment of cells with TSA during this time interval strongly inhibited HDAC activity, as shown by the threefold to fourfold increase of the acetylation signal in TSA-treated samples (Fig. 1B,C).

Although this temporal pattern of deacetylation was observed in four separate experiments, the intensity of the acetylation changes was variable from experiment to experiment. For this reason, a densitometric analysis of the chemiluminescent signal was performed, and the average values from the separate determinations are shown in Figure 1C. Each acetylated band was scanned, and the densitometric value was normalized to the actin content. The level of acetylation in the bFGF sample was arbitrarily defined as 100%. The acetylation signal of the samples harvested at different time points after mitogen removal was then represented as a percentage of the value in the presence of bFGF (Fig. 1C). Interestingly, at 6 hr, the average acetylation of H3 was 53%, and the average of H4 was 44% of the values determined in progenitor cells. At 24 hr, the average intensity of the acetylation signal decreased even further, reaching 28% of the original values for H3 and 13% for H4. Finally, at 48 hr, the average acetylation signal for H3 was 36% and for H4 was 30% of the initial levels.

To exclude the possibility that the decreased histone acetylation signal observed during oligodendrocyte lineage progression was attributable to decreased histone levels, cell lysates were harvested at distinct time points and analyzed for protein content by Western blot analysis using antibodies against total histones. As shown in Figure 2, the steady-state protein levels of histones H3, H2A, H2B (Fig. 2A), and histone H4 (Fig. 2B) did not change significantly during the time period examined in this study. We therefore concluded that the decreased histone acetylation signal was not attributable to significant changes in protein levels.



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  		Figure 2.   Changes in chromatin components during oligodendrocyte lineage progression. A, The steady-state levels of histones H2A, H2B, and H3 do not change during oligodendrocyte lineage progression. Protein lysates were obtained from proliferating progenitors cultured in bFGF (0) and from cells cultured for 6 (6), 24 (24), or 48 (48) hr in the absence of this mitogen. After separation by electrophoresis, the blots were probed with a mixture of three antibodies recognizing total histones H3, H2A, and H2B. Controls for loading of proteins were obtained probing the same blot for actin. B, The steady-state levels of histone H4 do not change during oligodendrocyte lineage progression. Protein lysates were obtained from proliferating progenitors cultured in bFGF (0) and from cells cultured for 6 (6), 24 (24), or 48 (48) hr in the absence of this mitogen. After separation by electrophoresis, the blots were probed with antibodies recognizing total histone H4. Reprobing with actin was used as loading control. C, Histones H3 and H4 are deacetylated. Protein lysates isolated from progenitor cells cultured in the presence of bFGF (0) or in the absence of mitogens for 24 or 48 hr, with (TSA) or without (24, 48) trichostatin A, were immunoprecipitated using anti-acetyl lysine antibodies (i.p. ac-lys). The blots were probed using anti-histone H3 and anti-histone H4 antibodies. D, Histone H2A and HMGN1 are deacetylated. Protein lysates were obtained from cells cultured in the conditions described in C. Samples were immunoprecipitated using antibodies recognizing acetyl lysine residues and then probed with anti-H2A, -H2B, -HMGN1, and -HMGN2 antibodies. The presence of H2A, H2B, HMGN1, and HMGN2 in the cells before immunoprecipitation was evaluated by including a whole cell lysate control (wcl).

To determine whether the changes in the acetylation during oligodendrocyte differentiation were attributable exclusively to deacetylation of lysine residues in nucleosomal histones (i.e., H2A, H2B, H3, and H4) or also affecting other chromatin proteins of the high-mobility group (i.e., HMGNs), we performed immunoprecipitation followed by Western blot analysis. Protein lysates obtained from differentiating oligodendrocyte progenitors were immunoprecipitated with antibodies against acetyl lysine, and the acetylated bands were then identified by Western blot analysis using antibodies recognizing histones H3 and H4 (Fig. 2C), histones H2A and H2B (Fig. 2D), or the high-mobility group proteins HMGN-1 and HMGN-2 (Fig. 2D). Interestingly, not all of the chromatin proteins were affected by HDAC activity during the onset of oligodendrocyte differentiation. Histone H2B and the high-mobility group protein HMGN-2, for instance, although both were detected in cell lysates of oligodendrocyte progenitors, did not show any change in acetylation during oligodendrocyte differentiation (Fig. 2D).

Densitometric analysis of the acetylation signal of H3 at 24 hr revealed a decrease to 23% of the values observed in progenitors. A similar decrease in acetylation during the first 24 hr of differentiation was also observed for HMGN-1, in which levels were reduced to 27% of the initial values. In contrast, the changes of H2A were of much smaller entity because, at 24 hr, the acetylation signal was still 70% of the progenitor values. From these data, we conclude that HDAC activity in differentiating oligodendrocytes is primarily directed to lysine residues in the tail of nucleosomal histones H4 and H3 and of the high-mobility group protein HMGN-1.

Inhibition of histone deacetylation with TSA prevents branching associated with oligodendrocyte progenitor lineage progression

To establish the functional significance of histone deacetylation during oligodendrocyte development, differentiation of progenitors was evaluated in the presence of increasing doses of the pharmacological inhibitor of HDAC TSA. Untreated progenitors differentiate very fast in response to mitogen withdrawal, and, within 24 hr, cells are characterized by the outgrowth of several fine cellular processes and a complex morphology (Fig. 1A). Treatment of differentiating progenitors with increasing concentrations of TSA progressively inhibited the formation of cellular branches (Fig. 3A). A quantitative analysis of the effect of the inhibitor on process outgrowth revealed a gradual shift of the prevalent phenotype with increasing doses of TSA. We observed a change from the complex morphology of untreated progenitors, to the intermediate phenotype of cells treated with 1 ng/ml TSA, to the simple morphology of cells treated with 10 ng/ml TSA (Fig. 3C). The progressive effect of increasing concentrations of TSA on morphological differentiation (Fig. 3A,C) correlated with a detectable increase in the acetylation signal (Fig. 3B).



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  		Figure 3.   Inhibition of histone deacetylation prevents morphological differentiation of oligo progenitors. A, Dose-dependent effect of TSA in preventing morphological changes associated with differentiation. Photomicrograph of progenitors cultured for 1 d in the absence of TSA or in the presence of 0.1 ng/ml (b), 1 ng/ml (c), or 10 ng/ml (d) TSA. The green immunofluorescence indicates O4-positive cells. The blue immunofluorescence (DAPI) identifies all cell nuclei. Cells treated with increasing doses of TSA display a progressively simpler morphology. B, Dose-dependent effect of TSA in inducing changes in acetylation. Western blot analysis of protein lysates obtained from cells treated for 24 hr with 0.1, 1, or 10 ng/ml TSA (+TSA). After SDS-PAGE, the blots were probed with anti-acetyl lysine antibodies. C, Quantitation of the TSA effect on the morphology of cells. Oligodendrocyte progenitors were allowed to differentiate by removal of mitogens from the medium containing 0.1, 1, or 10 ng/ml TSA for 24 hr. After staining live with O4, cells were fixed, processed by immunofluorescence, and then classified in each of the following categories: simple morphology, intermediate morphology, or complex morphology. Cells were classified as simple morphology if they only had short primary branches and bulky processes. Cells were classified as intermediate morphology if they had long primary or secondary branches. Cells were classified as complex morphology if they had tertiary branches. D, Effect of sodium butyrate on the morphology of the cells. Oligodendrocyte progenitors were treated with either 0.5 mM (a) or 5 mM (b) sodium butyrate. Only concentrations that are known to inhibit histone deacetylase (b) have an effect on progenitors morphology.

The effect of TSA on morphological differentiation of progenitors was observed also with other inhibitors of histone deacetylase, such as sodium butyrate. Lower concentrations of the drug (0.5 mM) did not affect process outgrowth (Fig. 3D). However, at a concentration known to inhibit HDAC activity (5 mM), sodium butyrate induced morphological changes similar to the ones induced by TSA. Also in this case, the outgrowth of the characteristic fine and complex branches was replaced by the formation of few bulky and thick cytoplasmic processes (Fig. 3D).

To begin to characterize the effect of the HDAC inhibitor on oligodendrocyte branching, we asked what was the minimum duration of the treatment resulting in stable alterations of process outgrowth. For this purpose, cells were induced to differentiate in mitogen-free medium containing 10 ng/ml TSA for the first 6, 12, or 24 hr of culture and then kept in medium without TSA for an additional 24 hr. As shown in Figure 4, the effect of TSA on the morphology of the cells was most evident after 24 hr of treatment. By this time, >90% of the cells exhibited a simple morphology. Together, these results suggest that HDAC activity is required for the induction of the morphological changes characteristic of differentiated oligodendrocytes.



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  		Figure 4.   The effect of TSA is time dependent. A, Population analysis of the TSA-dependent effect. Photomicrograph of O4-positive cells cultured for 48 hr in medium without mitogens (a, -TSA) or cultured for 6 hr (b), 12 hr (c), or 24 hr (d) in the presence of 10 ng/ml TSA, followed by an additional 24 hr of culture in the absence of TSA. Cells were fixed and stained for O4. Stable changes were observed only after 24 hr treatment. B, Quantitation of the TSA-dependent effect. O4-positive cells were analyzed under a fluorescence microscope and classified as either simple, intermediate, or complex morphology, as described in Figure 3C. The bar graph represents the results of the counts from four to six determinations resulting from two or three experiments each performed in duplicate.

TSA treatment is effective in preventing differentiation only if initiated during a specific temporal window

The time course of histone deacetylation, immediately preceding the onset of oligodendrocyte differentiation, suggested the possible existence of a temporal window of responsiveness of progenitors to differentiative stimuli (Fig. 5A). This hypothesis predicts that inhibition of histone deacetylation will prevent differentiation only during a specific time frame. To test this hypothesis, we started a 24 hr treatment with TSA at several time points after mitogen withdrawal. Cells were allowed to differentiate in mitogen-free medium for 6, 12, 24, 48, and 72 hr in the absence of TSA and were then kept for 24 hr in medium containing 10 ng/ml TSA. At the end of the treatment, cells were fixed, stained with O4, and assessed for morphological differentiation. As predicted by our hypothesis, the effect of TSA in preventing the acquisition of the complex branched morphology was observed only if treatment was started during the first 48 hr of mitogen withdrawal (Fig. 5A,B). However, the earlier start of the treatment correlated with a more prominent effect of TSA on branching. If treatment was initiated at the time of mitogen withdrawal, the cells displayed a very simple morphology after 1 d (Fig. 5A, d). The simple morphology was retained by the cells even after 4 d of treatment (Fig. 5C). Similar results were obtained when the treatment was started 6 hr after the removal of mitogens (Fig. 5B). However, when TSA was added to the medium after the cells had began to emit long primary branches (i.e., after 12 or 24 hr of culture in mitogen-free medium), the cells did not revert to a simpler morphology and did not elaborate additional processes. Therefore, they were characterized as "intermediate phenotype" (Fig. 5B). Finally, the start of treatment after differentiation had occurred (i.e., after 72 or 96 hr of culture in mitogen-free medium) did not revert the cells to a simpler phenotype. In this case, TSA-treated cells displayed the typical branching and membrane sheets (Fig. 5A, f) characteristic of mature oligodendrocyte (Fig. 5A, e). From these results, we conclude that TSA is not effective after the differentiation program has been initiated but prevents the progression to a mature phenotype if deacetylation is inhibited during the first 24-48 hr after mitogen withdrawal.



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  		Figure 5.   The effect of TSA in preventing morphological differentiation depends on when the treatment started. A, Effect of TSA on the morphology. Cells were cultured for 24 hr in the presence of TSA (b, d, f) or in its absence (a, c, e) and then stained for O4 (a, d) and PLP (e, f). TSA treatment did not change the morphology of progenitors cultured in bFGF (a, b). In addition, TSA treatment neither "reverted" the branching of cells cultured for 72 hr in the absence of mitogens (e, f) nor affected the expression of PLP by these cells. B, Quantitation of the effect of 24 hr TSA treatment started at different time points on the morphology of the cells. Oligo progenitors were cultured in medium without mitogens for 6, 12, or 24 hr (-TSA) and then treated with TSA for the next 24 hr (+TSA). After staining with the O4 marker, cells were analyzed by immunofluorescence and classified according to their morphology. Note that the effect of TSA on the morphology of the cells occurs only if the treatment is started early after mitogen withdrawal. C, Effect of 4 d treatment. Treatment of cells with 10 ng/ml TSA for 4 d completely prevented branching when it was started immediately after mitogen withdrawal.

Inhibition of histone deacetylation with TSA prevents the synthesis of oligodendrocyte differentiation markers

The effect of TSA treatment on morphological branching suggested that inhibiting histone deacetylation prevented the acquisition of a differentiated phenotype, although it did not address whether the expression of specific differentiation genes was also inhibited. To test the role of HDAC activity in oligodendrocyte differentiation, we therefore characterized the expression profile of stage-specific markers in the absence and presence of TSA. Untreated oligodendrocyte progenitors cultured in bFGF are characterized by the presence of the surface antigen A2B5 and the lipid sulfatide O4 (Bansal et al., 1989). When these cells are induced to differentiate by mitogen withdrawal, they lose A2B5 immunoreactivity and begin to express myelin components. GalC, the major lipid in myelin, is typically expressed between 48 and 72 hr, whereas PLP is expressed after 96-120 hr. TSA-treated cells, in contrast, did not lose A2B5 immunoreactivity and did not express the myelin components GalC and PLP, even 120 hr after mitogen withdrawal (Fig. 6A). Loss of PLP immunoreactivity occurred in the vast majority of the TSA-treated cells (Fig. 7). To determine whether decreased PLP immunoreactivity was attributable to decreased RNA levels, we used an RT-PCR. Consistent with an effect of TSA in modulating gene expression by affecting histone acetylation, decreased levels of PLP and GalC in the TSA-treated cells correlated with decreased RNA levels (Fig. 6B) for PLP and CGT (i.e., the synthetic enzyme responsible for the production of GalC). These data suggest that presumptive chromatin changes attributable to histone deacetylation are necessary for the expression of oligodendrocyte differentiation markers.



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  		Figure 6.   Treatment of oligodendrocyte progenitors with TSA arrests the cells at an immature stage of differentiation. A, TSA prevents the expression of late oligodendrocyte differentiation markers. To test the effect of histone deacetylation on the synthesis of lineage-specific markers, progenitors were cultured for 5 d without mitogens in the absence (-TSA) or presence (+TSA) of TSA. Cells were then processed for immunocytochemistry using antibodies against A2B5 (red, a, b), O4 (red, c, d), GalC (green, e, f), and PLP (green, g, h). Cell nuclei were visualized using DAPI (blue fluorescence in a-h). Typically, after 5 d of mitogen withdrawal, control cells have lost immunoreactivity for the progenitor marker A2B5 (a) but express O4 (c), GalC (e), and PLP (g). Preventing histone deacetylation with TSA halters the progression from progenitors to mature oligodendrocytes. TSA-treated cells do not express GalC and PLP (f, h) but express O4 (d) and the progenitor marker A2B5 (b). Scale bar, 20 µm. B, TSA lowers the RNA levels of CGT and PLP. To determine whether the lack of GalC and PLP immunoreactivity in TSA-treated cells was attributable to an effect on the RNA levels, a semiquantitative RT-PCR was performed. Briefly, RNA was isolated from untreated progenitors cultured in bFGF (bFGF) or differentiated in mitogen-free medium for 1 d (1d) or 3 d (3d). For TSA-treated cultures, the inhibitor was kept in the medium for 1 d (1d + TSA) or 3 d (3d + TSA) after mitogen withdrawal. After conversion into cDNA, the same amount was amplified using primers specific for actin, CGT, and PLP.



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  		Figure 7.   Inhibition of histone deacetylase activity prevents the progression of O4+ cells to a mature phenotype. A, TSA treatment prevents branching and PLP expression. Oligodendrocyte progenitors were allowed to differentiate by removing the mitogens from the culture medium in the absence (a, c, e) or presence (b, d, f) of 10 ng/ml TSA. The medium was replaced every other day, and, after 4 d, cells were stained with antibodies against O4 (red immunofluorescence in a, b and e, f) and PLP (green immunofluorescence in c, d and e, f). DAPI (blue immunofluorescence) was used to identify cell nuclei. B, TSA treatment reduces the proportion of cells expressing PLP. After immunohistochemistry, treated and untreated cells were examined under a fluorescence microscope, and three fields were counted from three distinct experiments, each performed in duplicate. The bar graphs represent the results of the quantitation.

The effect of histone deacetylation inhibition on oligodendrocyte differentiation is independent of cell cycle exit

The inhibitory effect of TSA on oligodendrocyte lineage progression could have been attributable to a direct effect of histone deacetylation on the differentiation program itself or to an indirect effect on proliferation. To distinguish between these two possibilities, we labeled cells in S phase with the thymidine analog BrdU and then counted the number of BrdU-positive cells in TSA-treated and untreated cultures. Briefly, progenitors were cultured in the presence of bFGF or in the absence of mitogen for 6, 12, 24, and 48 hr. All cultures were labeled with 10 µM BrdU during the last 6 hr before the end of the experiment. Cells were then fixed and double stained with antibodies against BrdU and against specific progenitor markers (i.e., A2B5 and O4). The number of A2B5+/BrdU+ cells and O4+/BrdU+ cells (Fig. 8A) was counted, and the percentage of BrdU-incorporating cells was calculated by dividing the number of double-labeled cells by the total number of A2B5+ and O4+ cells (Fig. 8B). The percentage of cells in S phase was similar in TSA-treated and untreated progenitors cultured in bFGF (Fig. 8A,B). A similar percentage of proliferating cells was also observed in TSA-treated and untreated cells after 6 and 12 hr of mitogen withdrawal. Interestingly, TSA-treated cells showed a faster kinetic of withdrawal from the cell cycle, because 100% of the treated cells exited the cell cycle at 24 hr, whereas 30% of the untreated cells was still proliferating (Fig. 8B). This effect was likely attributable to increased levels of the cell cycle inhibitor p21waf-1 (Fig. 8C) in TSA-treated cells, which is consistent with reports in other cell types (Yoshida et al., 1995; Sowa et al., 1999; Xiao et al., 1999). From these results, we conclude that the inability of oligodendrocyte progenitors to differentiate in the presence of HDAC inhibitors was not attributable to increased proliferation.



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  		Figure 8.   Inhibition of histone deacetylation blocks differentiation but not cell cycle exit. A, BrdU incorporation in TSA-treated cultures. Progenitors were kept proliferating in the presence of bFGF (a, b) or were allowed to differentiate by removing the mitogen from the medium (c, d) in the presence (b, d) or absence (a, c) of 10 ng/ml TSA. Cells in S phase were pulse labeled for 6 hr with 10 µM BrdU at 6, 12, 24, and 48 hr and then identified by positive immunoreactivity for BrdU (red) and O4+ (green) to identify proliferating cells. DAPI (blue) was used to identify all the cell nuclei. Scale bar, 20 µm. B, TSA treatment does not increase the number of cells in S phase. The number of double-labeled O4+/BrdU+ cells was counted and expressed as a percentage of the total number of O4+ cells. The gray bars represent the number of proliferating cells in the untreated cultures, whereas the black bars represent the number of proliferating cells in the TSA-treated cultures. C, The RNA levels of the cell cycle inhibitor p21 are increased by TSA. RNA was isolated from progenitors cultured in the absence or presence of 10 ng/ml TSA. Amplification of the mRNA was performed by semiquantitative RT-PCR. Actin levels were measured as internal control.

Removal of histone deacetylase inhibition allows recovery of morphological branching but not the synthesis of late differentiation markers

The acetylation state of nucleosomal histones is a reversible event because acetyl groups are transferred to lysine residues by the activity of acetyltransferases and removed by the activity of histone deacetylases. TSA inhibits the removal of acetyl groups from the histone tails, and, presumably, the activity of HDAC is restored immediately after removal of the drug, unless histone modifications have induced more permanent changes in chromatin conformation. To test the reversibility of TSA effect, progenitors were treated during the first 24 hr of mitogen withdrawal and then the drug was washed away, and the cells were kept in mitogen-free medium for a total of 3 or 5 d. After this recovery time, cells were fixed, stained, and then analyzed for branched morphology and myelin gene expression (Fig. 9). Three days after mitogen withdrawal, untreated cells were highly branched and expressed both lipid sulfatides (identified by O4 immunoreactivity) and galactocerebrosides (identified by GalC immunoreactivity). At the same time point, cells that were treated with TSA during the first 24 hr showed shorter cellular processes and barely detectable levels of GalC. Five days after mitogen withdrawal, untreated cells expressed high levels of PLP and had developed extensive myelin sheets (Fig. 9A). At the same time point, however, cells that were treated with TSA for the first 24 hr did not elaborate complex membranes and expressed very low levels of PLP (Fig. 9A). Interestingly, a Western bot analysis of cell extracts obtained from cells at distinct recovery times reveals fast deacetylation kinetics after the removal of the drug (Fig. 9B). These data suggested that the effects of preventing histone deacetylation during the first 24 hr of mitogen withdrawal are only partially reversible.



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  		Figure 9.   The effect of TSA treatment on morphological differentiation of progenitors is reversible. A, Recovery after TSA washout. Oligodendrocyte progenitors were allowed to differentiate in the absence of TSA by withdrawal of mitogen from the medium for either 3 d (a, e, i) or 5 d (c, g, k). The TSA-treated group was exposed to 10 ng/ml TSA during the first 24 hr of mitogen withdrawal and then allowed to recover for an additional 2 d (b, f, j) or 4 d (d, h, l) in the absence of the drug. Cells cultured for 3 d (a-j) were stained with antibodies against O4 (red) and GalC (green), whereas the nuclei were identified using DAPI (blue). Cells cultured for 5 d were stained with antibodies against O4 (red) and PLP (green). Note that the alterations of the cell morphology induced by TSA were completely reversible, whereas the expression of myelin-specific genes was weaker in cells treated with TSA during the first 24 hr of mitogen withdrawal. Scale bar, 20 µm. B, Recovery of deacetylation after TSA washout. Western blot analysis of protein lysates obtained from cells treated for 1 d with 10 ng/ml TSA (0) and from cells allowed to recover in the absence of TSA for 1 d (1d), 2 d (2d), or 3 d (3d). Note that, after removal of the HDAC inhibitor from the medium, deacetylation occurs quite rapidly, and this correlates with the recovery of branching.

TSA blocks the progression of progenitors into oligodendrocytes but not into astrocytes

Cortical oligodendrocyte progenitors have the ability to differentiate in vitro into oligodendrocytes, when cultured in the absence of mitogens, or into type II astrocytes, when cultured in the presence of serum. The results described above show that histone deacetylation was necessary for oligodendrocyte differentiation. We now asked whether histone deacetylation was crucial also for the progression into type II astrocytes. Progenitors were cultured in serum containing medium with or without TSA for 7-10 d and then stained for GFAP (Fig. 10). In the presence of bFGF or after the removal of mitogens, progenitors do not express GFAP (data not shown). However, after 7-10 d of culture in medium containing 20% serum, cells can be identified as "protoplasmic" astrocyte or type II astrocytes, characterized by a stellate morphology with thick cytoplasmic processes and GFAP expression. Interestingly, the presence of TSA in the medium did not affect the morphology or the expression of astrocyte markers and were virtually indistinguishable from untreated controls (Fig. 10). We conclude that histone deacetylation is a specific event occurring during differentiation of bipotential progenitors into the oligodendrocyte but not into the astrocyte lineage.



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  		Figure 10.   Inhibition of histone deacetylase activity does not prevent differentiation of cortical progenitors into type IIA astrocytes. Rat cortical progenitors were differentiated into type II astrocytes cultured in medium supplemented with 20% FCS in the absence (a) or presence (b) of TSA and then stained for glial fibrillary acidic protein (green fluorescence). No difference was observed in either morphology or GFAP expression between treated and untreated cells.


    DISCUSSION

TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Histone deacetylation is necessary for oligodendrocyte differentiation

The mechanisms responsible for oligodendrocyte differentiation are still primarily not understood. Recent progress has been made in the identification of transcription factors regulating the specification of oligodendrocyte progenitors from multipotential neural stem cells, but the steps involved in the subsequent progression to a myelinating cell are still primarily not understood. Several lines of evidence have established the existence of an obligate relationship between cell cycle exit and differentiation. Although differences might exist between progenitors isolated from the optic nerve or from the cerebellar or cortical cortex (Ghiani and Gallo, 2001), it can be stated that the presence of mitogens favors cell division at the expenses of differentiation, whereas the absence of mitogens favors withdrawal from the cell cycle and oligodendrocyte differentiation (Noble and Murray, 1984; Temple and Raff, 1985). In addition, clonal analysis of single optic rat nerve progenitors indicated that, in the presence of specific extracellular signals, cells divide a certain number of times before they stop and differentiate (Temple and Raff, 1986; Barres et al., 1994). Finally, phenotypic analysis of mice with targeted deletions for genes encoding the cell cycle inhibitors p21-Waf1 or p27-Kip1 indicated that differentiation of oligodendrocyte progenitors was clearly impaired (Casaccia-Bonnefil et al., 1997, 1999; Zezula et al., 2001). These results led to the hypothesis that cell cycle inhibitors may be sufficient to induce differentiation of oligodendrocyte progenitors. However, when p27-Kip1 levels were increased in proliferating oligodendrocyte progenitors by treatment with neurotransmitters (Ghiani et al., 1999) or by viral gene transfer (Tikoo et al., 1998; Tang et al., 1999), the cells stopped proliferating but did not differentiate. Together, these data indicated that, besides cell cycle regulators, other elements might be required to start the oligodendrocyte transcriptional program of differentiation.

Studies in other lineages indicated that chromatin modifiers with histone acetyltransferase activity are necessary for the induction of terminal differentiation. The recruitment of coactivators such as p300 in a complex with other transcription factors is able to activate expression of neuronal and astrocytic genes.

Based on these studies, we asked whether histone acetylation could be a molecular mechanism that, together with molecules regulating cell cycle exit, modulates the access of transcription factors to the promoter regions of genes involved in oligodendrocyte differentiation. To test this hypothesis, we induced cell cycle exit by removing the mitogens from the culture medium. There are several advantages in using mitogen withdrawal as an experimental paradigm of oligodendrocyte differentiation. First, it allows the study of events "intrinsic" to the cell, in the absence of additional signals from the extracellular environment. Second, differentiation of progenitors proceeds in a sequence of temporally well defined stages, each characterized by specific morphological features and unique antigenic repertoire (Pfeiffer et al., 1993). Using this model system, we first showed that histone deacetylation, rather than acetylation, occurs in primary cortical oligodendrocyte progenitors during the temporal window preceding the onset of differentiation. We then addressed the necessity of this event for oligodendrocyte differentiation by testing the consequences of histone deacetylase inhibitors on oligodendrocyte lineage progression. Because the acetyl groups on nucleosomal histone tails are in a dynamic equilibrium based on the activity of HATs and deacetylases (e.g., HDACs), blockers of HDAC, such as TSA and sodium butyrate, increase the histone acetylation state (Fig. 3). Our data indicate that TSA prevented the progression of progenitors to mature oligodendrocytes (Figs. 3-7). Although we cannot formally exclude the possibility that TSA may act also on proteins other than nucleosomal histones, our data using antibodies directed against acetylated lysine residues detected changes only in proteins with a molecular weight between 9 and 18 kDa. These bands were further characterized by their immunoreactivity with antibodies against the nucleosomal histones H2A, H3, and H4 and the high-mobility group protein HMGN-1. In addition, several studies in other cell types have indicated the specificity of TSA on the inhibition of HDAC activity at the concentrations used in our studies (Yoshida et al., 1990, 1995). Finally, additional data on the specificity of TSA as inhibitor of HDAC have been provided by the recent crystal structure of the histone deacetylase catalytic core bound to TSA (Finnin et al., 1999). Together, these evidences validate the use of TSA as a specific inhibitor of HDAC enzymatic activity.

Bulk histone deacetylation is transiently observed during oligodendrocyte differentiation

Although histone acetylation-deacetylation has been shown to regulate the activity of specific promoter regions, this is the first study to our knowledge of bulk histone deacetylation associated with differentiation of progenitor cells. Because deacetylation of nucleosomal histones is associated with repressed chromatin structure, the detection of this event during a specific temporal window after mitogen withdrawal and before onset of differentiation raises several questions. Does repression occur during oligodendrocyte lineage progression? If so, what is the extent of transcriptional repression event? The importance of transcriptional repression in oligodendrocyte lineage progression is supported by numerous studies describing progressive loss of specific gene products during normal oligodendrocyte development. There is general consensus regarding downregulation of specific surface antigens (Raff et al., 1984), transcription factors (Wegner, 2001), differentiation inhibitors (Kondo and Raff, 2000), growth factor receptors (Hart et al., 1989; Ellison and de Vellis, 1994; Bansal et al., 1996; Rodriguez-Pena, 1999), guidance molecules, and cell cycle genes (Casaccia-Bonnefil et al., 1997; Huang et al., 2002) during oligodendrocyte differentiation. In vivo, this decrease in gene expression occurs gradually, whereas in vitro, the withdrawal of mitogens accelerates timing of differentiation, therefore "condensing" changes in gene expression within a much shorter timeframe. This "synchronized" repression of multiple genes could explain the "bulk" histone deacetylation observed in our study.

A proposed model of the role of histone deacetylation in oligodendrocyte differentiation

Our observations suggest that histone deacetylation is required for differentiation of oligodendrocyte progenitors. Because histone deacetylation is associated with chromatin compaction, we propose two models to explain the role possibly played by chromatin remodeling in oligodendrocyte differentiation. According to one model, compaction of chromatin may occur on negative regulatory sites of differentiation genes (Fig. 11A). According to this model, the promoter activity of specific differentiation genes, such as PLP, is maintained low in progenitor cells (Timsit et al., 1995; Dickinson et al., 1996; Mallon et al., 2002) by the interaction of specific repressors binding negative regulatory sites in the promoter region (Berndt et al., 1992; Wight et al., 1997). Histone deacetylation in these regions would result in chromatin compaction and difficult access of repressors to these negative regulatory elements. This change of conformation therefore reduces repression and results in increased levels of expression in the gene product (Fig. 11A). According to an alternative model, chromatin compaction may occur in the promoter region of genes encoding for inhibitors of differentiation site (i.e., Ids) (Kondo and Raff, 2000), thereby blocking the access of the transcriptional apparatus to the START site. In this case, chromatin compaction may be responsible for the decreased levels of molecules known to sequester activators of myelin gene expression, such as the Ids (Fig. 11B). These models are not mutually exclusive and may well both occur within the same cell at a given time.



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  		Figure 11.   A proposed model of the role of histone deacetylation in oligodendrocyte differentiation. A, Direct model. The first model assumes that histone deacetylation occurs directly in the promoter of specific differentiation genes (e.g., myelin genes). In the presence of mitogens, nucleosomal histones are acetylated on lysine residues (orange circles with COO- tails), and this results in open chromatin conformation and exposure of negative regulatory sites (green rectangles) in the promoter region of myelin genes. Binding of specific regulatory molecules (black ovals) to these sites is favored, and progenitors are kept in an undifferentiated state. On recruitment of HDAC, induced by the withdrawal of mitogens, histone tails are deacetylated (orange circles with no tails), and the chromatin around the negative regulatory sites is compacted, thus preventing the access to transcriptional inhibitors. This event results in onset of differentiation caused by compaction of negative cis-element on the promoter region of myelin genes. B, Indirect model. The second model predicts that histone deacetylation occurs on the promoter of genes encoding for differentiation inhibitors (e.g., gene X). In progenitor cells, nucleosomal histones in the promoter region of the differentiation inhib-itor are acetylated (orange circles with COO- tails), resulting in open chromatin conformation and expression of the inhibitor X. This in turn may bind to negative regulatory sites on differentiation genes and prevent their expression. Onset of differentiation in this case is initiated by recruitment of HDAC to the promoter region, resulting in chromatin compaction and decreased expression of the differentiation inhibitor. According to this model, the negative element on the promoter of differentiation genes may be acetylated but inactive, because of the absence of gene X (left), or deacetylated and compacted (right). In both cases, the expression of differentiation genes is activated by histone deacetylation.

Concluding remarks

In conclusion, we identified histone deacetylase activity as necessary for oligodendrocyte differentiation. This mechanism involves deacetylation of chromatin components and is followed by presumptive chromatin remodeling. Blocking deacetylation prevents differentiation and suggests that transcriptional repression is a crucial event during oligodendrocyte lineage progression. A better understanding of these molecular events will allow the design of therapies targeted at efficient remyelination.


    FOOTNOTES

Received May 21, 2002; revised Aug. 30, 2002; accepted Sept. 13, 2002.

This work was supported by the Wadsworth Foundation (P.C.B.) and National Multiple Sclerosis Society Grants RG 3154-A-2 (P.C.B.) and FA 1512-A-1 (M.M.H.). We thank Drs. N. Hayes and E. Di Cicco-Bloom for critical reading of this manuscript, Dr. D. Reinberg for advice and reagents, and Dr. M. Bustin for antibodies.

Correspondence should be addressed to Patrizia Casaccia-Bonnefil, Department of Neuroscience and Cell Biology, University of Medicine and Dentistry of New Jersey, 675 Hoes Lane, Piscataway, NJ 08854. E-mail: casaccpa{at}umdnj.edu.


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ABSTRACT
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RESULTS
DISCUSSION
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