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The Journal of Neuroscience, May 11, 2005, 25(19):4706-4718; doi:10.1523/JNEUROSCI.4520-04.2005
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Development/Plasticity/Repair
The Neurosteroid Allopregnanolone Promotes Proliferation of Rodent and Human Neural Progenitor Cells and Regulates Cell-Cycle Gene and Protein Expression
Jun Ming Wang,1
Patrick B. Johnston,2
Bret Gene Ball,3 and
Roberta Diaz Brinton1
1Department of Molecular Pharmacology and Toxicology and Program in Neuroscience, Pharmaceutical Science Center, University of Southern California, Los Angeles, California 90033, 2Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905, and 3Gene Therapy Laboratories, Department of Biochemistry, Keck School of Medicine, University of Southern California, Los Angeles, California 90033
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Abstract
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Our previous research demonstrated that the neuroactive progesterone metabolite allopregnanolone (3 -hydroxy-5-pregnan-20-one) rapidly induced hippocampal neuron neurite regression (Brinton, 1994 ). We hypothesized that allopregnanolone-induced neurite regression was a prelude to mitogenesis initiated by a rise in intracellular calcium. Supporting this hypothesis, the current data demonstrate that allopregnanolone, in a dose-dependent manner, induces a significant increase in proliferation of neuroprogenitor cells (NPCs) derived from the rat hippocampus and human neural stem cells (hNSCs) derived from the cerebral cortex. Proliferation was determined by incorporation of bromodeoxyuridine and [3H]thymidine, fluorescence-activated cell sorter analysis of murine leukemia virus-green fluorescent protein-labeled mitotic NPCs, and total cell number counting. Allopregnanolone-induced proliferation was isomer and steroid specific, in that the stereoisomer 3 -hydroxy-5-pregnan-20-one and related steroids did not increase [3H]thymidine uptake. Immunofluorescent analyses for the NPC markers nestin and Tuj1 indicated that newly formed cells were of neuronal lineage. Furthermore, microarray analysis of cell-cycle genes and real-time reverse transcription-PCR and Western blot validation revealed that allopregnanolone increased the expression of genes that promote mitosis and inhibited the expression of genes that repress cell proliferation. Allopregnanolone-induced proliferation was antagonized by the voltage-gated L-type calcium channel (VGLCC) blocker nifedipine, consistent with the finding that allopregnanolone induces a rapid increase in intracellular calcium in hippocampal neurons via a GABA type A receptor-activated VGLCC (Son et al., 2002). These data demonstrate that allopregnanolone significantly increased rat NPC and hNSC proliferation with concomitant regulation in mitotic cell-cycle genes via a VGLCC mechanism. The therapeutic potential of allopregnanolone as a neurogenic molecule is discussed.
Key words: allopregnanolone; neurogenesis; hippocampus; cell-cycle genes; L-type calcium channel; therapeutics
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Introduction
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The neurosteroid allopregnanolone (AP) (3-hydroxy-5-pregnan-20-one) is a reduced metabolite of progesterone (P4) and is generated de novo in the CNS (for review, see Melcangi et al., 1999; Baulieu et al., 2001; Mellon and Griffin, 2002b). Developmentally, P4 and AP are synthesized in the CNS throughout the embryonic period in the pluripotential progenitor cells (Lauber and Lichtensteiger, 1996; Gago et al., 2004) and reach their highest concentration in late gestation (Pomata et al., 2000; Grobin and Morrow, 2001). In the aged and Alzheimer's disease (AD) brain, both the pool of neural stem cells (NSCs) and their proliferative potential are markedly diminished (Bernardi et al., 1998; Genazzani et al., 1998). In parallel, AP content is diminished in the brains of AD patients compared with age-matched controls (Weill-Engerer et al., 2002).
Functional analyses indicate that AP induces myelin formation in both the CNS and the peripheral nervous system (Baulieu and Schumacher, 2000; Schumacher et al., 2003) and promotes neuron survival in the presence of excitotoxic insults (Brinton, 1994; Ciriza et al., 2004). Griffin et al. (2004) recently reported that AP can delay the onset and severity of neurodegenerative pathology in a mouse model of Niemann-Pick's disease.
In mature neurons, AP is well known as an allosteric modulator of the GABAA receptor (GABAAR)/chloride channel to increase chloride influx, thereby hyperpolarizing the neuronal membrane potential and decreasing neuron excitability (Gee et al., 1992; Brinton, 1994; Grobin and Morrow, 2001; Liu et al., 2002). These properties led to the pursuit of AP and derivatives as an antiepileptic and antianxiety therapeutic drug (Monaghan et al., 1997; Kerrigan et al., 2000). In marked contrast, the flux of chloride in developing neurons is opposite to that of mature neurons (Cherubini et al., 1990; Perrot-Sinal et al., 2003). In immature neurons, the high intracellular chloride content leads to an efflux of chloride through the GABAAR depolarization of the membrane and opening of L-type voltage-gated Ca2+ channels (VGLCCs) (Dayanithi and Tapia-Arancibia, 1996; Son et al., 2002; Ben-Ari et al., 2004; van den Pol, 2004). Thus, the GABAAR-mediated depolarization could be a trigger for a spontaneous, activity-independent [Ca2+]i rise in early precursor cells or subventricular zone radial precursor cells, thereby influencing developmental events, such as neurogenesis and synaptogenesis (Owens et al., 2000; Ashworth and Bolsover, 2002; Deisseroth et al., 2004).
Previous work from our laboratory demonstrated that exposure of embryonic day 18 (E18) rat hippocampal neurons to AP induced regression of neurite outgrowth within 1 h (Brinton, 1994). Subsequent microscopic morphological observation indicated that AP significantly increased the number of cells exhibiting morphological features of mitotic events (our unpublished observations). These findings led us to hypothesize that AP promoted hippocampal progenitor cell proliferation to thereby act as a neurogenic agent. Therefore, we undertook a series of cellular, morphological, biochemical, and genomic analyses to determine the neurogenic potential of AP in cultured rat neural progenitor cells (rNPCs) and human NSCs (hNSCs).
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Materials and Methods
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Animals. Timed-pregnant Sprague Dawley rats were purchased from Harlan Sprague Dawley (Indianapolis, IN). These rats were housed at 24°C on a 14/10 h light/dark cycle, fed with regular rat chow, and allowed tap water ad libitum. All studies were approved by the University of Southern California Institutional Review Board for animal care.
Steroids. All steroids used in this study were purchased from Steraloids (Newport, RI). They are as follows: AP, epipregnanolone (AP) (5-pregnan-3-ol-20-one), epiallopregnanolone (5-pregnan-3-ol-20-one), P4, allopregnanediol (5-pregnan-3, 20-diol), allopregnanetriol (5-pregnan-3, 17, 20-triol), 5-pregnan-3-ol, and pregnenolone sulfate (5-pregnan-3-ol-20-one sulfate).
Hippocampal neuronal culture. Primary cultures of dissociated hippocampal neurons were performed as described previously (Nilsen and Brinton, 2003). Briefly, hippocampi were dissected from the brains of E18 rat fetuses, treated with 0.02% trypsin in HBSS (Invitrogen, Grand Island, NY) for 5 min at 37°C, and dissociated by repeated passage through a series of fire-polished constricted Pasteur pipettes. Cells were plated on poly-D-lysine-coated 60 mm Falcon Petri dishes at a density of 0.5-1 x 105 cells/cm2 for biochemical study. Cells were plated on Nalge Nunc (Naperville, IL) CC2-coated four-well chamber slides at a density of 2-4 x 104 cells/cm2 for morphological study or on laminin-coated cell culture-grade black clear-bottom 96-well Falcon plates at a density of 7.5-15 x 104 cells per well for 5-bromo-2-deoxyuridine (BrdU) incorporation chemiluminescence immunoassay. Nerve cells were grown in Neurobasal medium (Invitrogen, Carlsbad, CA) supplemented with 10 U/ml penicillin, 10 µg/ml streptomycin, 0.5 mM glutamine, 25 µM glutamate, and 2% B27 (Invitrogen, Gaithersburg, MD). Cultures were maintained at 37°C in a humidified 5% CO2 atmosphere. All experiments were performed at the times indicated.
Culture of human neural stem cells. Human embryonic brain cortical stem cells (gift from Dr. Svendsen, Departments of Anatomy and Neurology and the Waisman Center, University of Wisconsin, Madison, WI) were provided as cryopreserved neurospheres. Neurospheres were cultured as described previously by Dr. Svendsen's laboratory (Wachs et al., 2003) in DMEM/Ham's F-12 medium (7:3) containing penicillin/streptomycin/amphotericin B (1%), supplemented with B27 (2%; Invitrogen, Gaithersburg, MD), epidermal growth factor (EGF) (20 ng/ml; Invitrogen, Gaithersburg, MD), FGF-2 (20 ng/ml; Invitrogen, Gaithersburg, MD), and heparin (5 µg/ml; Sigma, St. Louis, MO) in a humidified incubator (37°C and 5% CO2), and one-half of the growth medium was replenished every 3-4 d. Neurospheres were then mechanically triturated into single cells with flame-polished Pasteur pipettes, plated onto T75 flasks at a density equivalent to 2 x 106 cells per flask, and passaged every 14 d. After the second passage, cells were switched to maintenance media [DMEM/Ham's F-12 (7:3)] containing N2 supplement (1%; Invitrogen), 20 ng/ml EGF, and 10 ng/ml LIF (Chemicon, Temecula, CA) and seeded onto T75 flasks coated with laminin (MP Biomedicals, Irvine, CA) at a density of 2 x 106 cells per flask, which were then plated onto laminin-coated 96-well plates at a density of 7.5-15 x 104 cells per well or chamber slides at a density of 2-4 x 104 cells/cm2 before analysis.
Immunocytochemical staining. Immunocytochemistry was performed to check the cell composition in the culture and determine the cell lineage of the newly formed neurons. Hippocampal neurons, plated onto four-well chamber slides and allowed to seed for 1 h, were treated with 250 nM AP or vehicle for times as indicated in Results and fixed with 4% paraformaldehyde. Neurons were then incubated overnight with the following primary antibodies (Doetsch et al., 1997; Romero-Ramos et al., 2002): monoclonal antibody for neuronal class III -tubulin [Tuj1; 1:500 (NPC marker); Covance, Berkeley, CA], monoclonal antibody for nestin [1:5000 (NSC marker); Chemicon], monoclonal antibody for myelin basic protein (MBP) [1:50 (oligodendrocyte marker); Research Diagnostics, Flanders, NJ], polyclonal antibody for glial fibrillary acidic protein (GFAP) [1:1000 (astrocyte marker); Santa Cruz Biotechnology, Santa Cruz, CA], and monoclonal antibody for microtubule-associated protein 2 (MAP2) [1:200 (neuronal cell marker); Sigma] for colabeling with GFAP or polyclonal antibody for MAP2 (1:1000; Chemicon) for colabeling with other mice-derived antibodies. After PBS wash, cells were incubated for 30 min in a mixture of secondary antibodies containing anti-mouse IgG or anti-rabbit IgG conjugated with FITC (1: 200; Vector Laboratories, Burlingame, CA) and anti-rabbit IgG or anti-mouse IgG conjugated with Texas Red (1:50; Vector Laboratories) according to the requirements of the first antibody and colabeling combination. Slides were washed three times for 10 min each with PBS, rinsed with water, and mounted under coverslips with 4',6'-diamidino-2-phenylindole (DAPI)-containing mounting medium (Vector Laboratories). Labeled cells were observed by Zeiss (Oberkochen, Germany) Axiovert 200M fluorescent microscope, and images were captured by SlideBook software (Intelligent Imaging Innovations, San Diego, CA).
Human neuronal stem cells were plated into four-well chamber slides coated with laminin. The cells were immunostained for the neuronal stem cells markers nestin and Tuj1 as described above.
BrdU incorporation. Cell proliferation was first evaluated by measuring the incorporation of BrdU in the S phase of the cell cycle. BrdU incorporation was detected by using kits purchased from Roche (Penzberg, Germany). For immunofluorescent assay, cells were loaded with 10 µM BrdU after 1 h of seeding on chamber slides in the presence or absence of 250 nM AP and cultured for 1 d. After fixation with 4% paraformaldehyde, cells were then incubated with anti-BrdU working solution, a 1:10 dilution of antibody to incubation buffer (in mM: 66 Tris, pH 8.0, 0.66 MgCl2, and 1 2-mercaptoethanol), for 30 min at 37°C. Cells were then incubated with anti-mouse IgG conjugated with fluorescein (1:10 in incubation buffer) for 30 min at 37°C. Chamber slides were mounted, cells were observed, and the images were captured as described above. For chemiluminescence immunoassay, rat hippocampal cells, after 1 h of seeding, were loaded with 10 µM BrdU in the presence or absence of mouse EGF (20 ng/ml) and 100 pM to 1000 µM AP in Neurobasal medium with B27 for 1 d, and human cerebral cortical stem cells, after overnight adhesion and then 4-5 h of starvation (medium without supplements), were loaded with 10 µM BrdU in the presence or absence of basic FGF (bFGF) and a different concentration of AP in complete maintenance medium for 1 d. The cells were then fixed using the Fixdenat solution (Roche) for 30 min, incubated with anti-BrdU peroxidase for 90 min, and further developed with substrate solution for 3 min. The plates were then read with an Lmax microplate luminometer (Molecular Devices, Sunnyvale, CA). After subtracting the value of the blank (without BrdU loading), the results were analyzed using a one-way ANOVA, followed by a Neuman-Keuls post hoc test, and presented as percentage increase versus control.
[3H]thymidine uptake. The specificity of AP and its stereoisomers, as well as its parental neurosteroid progesterone, on DNA replication was determined by [3H]thymidine uptake. Briefly, hippocampal neurons (1 x 105 per well) were seeded in poly-D-lysine-coated 24-well Falcon plates. After 1 h, neurons were loaded with 1 µCi/ml [3H]thymidine in the presence or absence of 250 nM AP or its relative stereoisomers for 24 h. Neurons were washed three times with PBS to remove free [3H]thymidine and collected by a rubber policeman. Cell lysates were counted in a Beckman counter (LS1801; Beckman Coulter, Fullerton, CA). Data are presented as mean ± SEM of three independent experiments conducted in triplicate.
Murine leukemia virus-enhanced green fluorescent protein viral particle preparation and cell labeling. To verify that AP-induced DNA amplification was indicative of mitosis and not DNA repair and that AP led to a complete mitosis, fluorescence-activated cell sorting (FACS) assay was performed to quantitatively measure the number of retrovirusen-hanced green fluorescent protein (eGFP)-labeled dividing rNPCs (Palmer et al., 1997; van Praag et al., 2002). The murine leukemia virus (MuLV)-GFP retrovirus integrates into the host genome only if nuclear envelope breakdown occurs, which takes place during mitosis and hence does not occur under conditions of DNA repair during which BrdU can also be incorporated. More importantly, MuLV is unable to infect growth-arrested cells or cells progressing through a partial cell cycle that includes S phase but not mitosis (Roe et al., 1993; Lewis and Emerman, 1994; Bieniasz et al., 1995). Thus, the GFP signal can only be observed in the cells that have transversed a complete cell cycle. Importantly, MuLV is unable to infect growth-arrested cells or cells progressing through a partial cell cycle that includes the S phase but not mitosis (Roe et al., 1993; Lewis and Emerman, 1994; Bieniasz et al., 1995). Therefore, an increase in the number of GFP-positive cells serves not only as a marker for proliferation but also as an indicator for complete mitosis.
Retroviral vector particles were produced by a three-plasmid expression system (Soneoka et al., 1995). In brief, 24 h before transfection, human embryonic kidney 293T (HEK293T) cells were split one to five and transferred to a 10 cm tissue culture plate. To transfect, 10 µg of retroviral vector containing GFP gene, which was constructed into a PGK-eGFP gene cassette between MuLV 5' long-term repeat (LTR) plus a packaging signal and 3' LTR (W. F. Anderson, University of Southern California, Los Angeles, CA); 10 µg of pCGP plasmid containing the viral gag pol genes, which encode the viral matrix, capsid, nucleoproteins, and reverse transcriptase (W. F. Anderson); and 10 µg of pCEE+ plasmid expressing the MuLV ecotropic envelope protein (MacKrell et al., 1996) were coprecipitated by calcium phosphate. The precipitate was added drop-wise to HEK293T cells at  75% confluence. Twelve to 16 h after transfection, cells were washed with PBS warmed to 37°C, and then fresh medium was added. Thirty-six hours after transfection, viral supernatants were harvested and passed through a 0.45 µm filter (Millipore, Bedford, MA) to remove transfected cells and cellular debris. Final virus titers (labeled MuLV-eGFP) were 5-7 x 106 colony-forming units per milliliter as determined by FACS (Coulter Epics-XL Fluorescence-Activated Cell Sorter) analysis of transduced HEK293T controls.
Rat hippocampal neurons were seeded onto 60 mm Petri dishes for FACS analysis or slide chambers for fluorescent microscopy observation and were infected with MuLV-eGFP viral particles (2.5-3.5 x 106/ml) in the presence or absence of 500 nM AP, 500 nM AP, 10 µM nifedipine, or nifedipine plus AP 1 h after seeding. After 4 h, cells were washed and further incubated with fresh media with steroids to allow for the GFP expression in infected cells.
HT-22 cell culture and MuLV-GFP infection. The immortalized mouse hippocampal HT-22 cell line (Sagara et al., 2002; Mize et al., 2003) was used as a positive control for labeling dividing cells by MuLV-GFP. Cells were cultivated in DMEM (high glucose, with L-glutamine, with pyridoxine hydrochloride; Invitrogen, Grand Island, NY) supplemented with 100 U/ml penicillin, 100 mg/ml streptomycin, and 5% FBS (heat inactivated). The cells were split 1-10 every 4 d. One day after splitting, the cells were infected with MuLV-GFP viral particles in the presence or absence of AP as described above.
FACS analysis and morphological observation of MuLV-GFP-positive cells. After 48 h of incubation, cells were trypsinized, suspended gently by pipetting up and down, and collected into a Falcon 12 x 75 mm tube (polystyrene). After fixation with 4% paraformaldehyde, the cells were then subjected to FACS analysis. In each sample, 2000 cells were sorted by Coulter Epics-XL Fluorescence Activated Cell Sorter, and the numbers of GFP-positive cells were given. The mouse hippocampal derived cell line HT-22 was used as a positive control, whereas primary 7 d in vitro (DIV) hippocampal neurons, which were without detectable mitotic activity as measured by BrdU labeling, were used as a negative control. The neuronal morphology of the GFP-positive cells was assessed using cells seeded on chamber slides. In addition, cells were immunostained with the NPC cell marker Tuj1 as described above.
Gene-array assay. To analyze cell-cycle gene regulation, a commercially available targeted cDNA array of 96 cell-cycle regulatory genes and two housekeeping genes (Cell Cycle GEArray Q series, version 1; Super-Array, Bethesda, MD) were used according to the instructions of the manufacturer. Briefly, primary cultures were treated with or without 500 nM AP for 24 h, and total RNA was isolated using TRIzol reagent (Invitrogen, Carlsbad, CA) as described by the manufacturer. Ten micrograms of total RNA were reverse transcribed into biotin-16-deoxy-UTP-labeled single-strand cDNA by Moloney murine leukemia virus reverse transcriptase. After prehybridization, membranes were hybridized with biotin-labeled cDNA probe and incubated with alkaline phosphatase-conjugated streptavidin. Chemiluminescence was visualized by autoradiography. The intensity of the spots was extracted using "ScanAlyze" software [developed by Michael Eisen at Lawrence Berkeley National Laboratory (Berkeley, CA), recommended by SuperArray]. The data were analyzed by GEArray Analyzer (SuperArray, version 1.3). -Actin and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were used as internal controls. Bacterial plasmid (pUC18) was used as a negative control.
Real-time reverse transcription-PCR. Real-time reverse transcription (RT)-PCR was performed to validate the gene-array results. Total RNA was prepared as described above. cDNA was synthesized using Super-Script III reverse transcriptase (Invitrogen, Grand Island, NY) and oligo-dT primer in accordance with the protocols of the manufacturer. The expression of related genes was quantified using the SYBR green reagent (2x SYBR Green Supermix; Bio-Rad, Hercules, CA) following the instructions of the manufacturer on a Bio-Rad iCycler. PCR was performed in multiplicate in optimized conditions: 95°C denatured for 3 min, followed by 40 cycles of 45 s at 94°C, 45 s at 55°C, and 45 s at 72°C using the following primers: cyclin A2 (GenBank accession number XM_342229), forward, 5'-GCTTTTAGTGCCGCTGTCTC-3', reverse, 5'-AGTGATGTCTGGCTGCCTCT-3'; cyclin B1 (GenBank accession number NM_171991
[GenBank]
), forward, 5'-CTGCTGCAGGAGACCATGTA-3', reverse, 5'-CTACGGAGGAAGTGCAGAGG-3'; cyclin E (GenBank accession number D14015
[GenBank]
), forward, 5'-ATGTCCAAGTGGCCTACGTC-3', reverse, 5'-TCTGCATCAACTCCAACGAG-3'; cell-dividing control protein 2 (CDC2) (GenBank accession number NM_019296
[GenBank]
), forward, 5'-CGGTTGACATCTGGAGCATA-3', reverse, 5'-GCATTTTCGAGAGCAAGTCC-3'; proliferating cell nuclear antigen (PCNA) (GenBank accession number NM_022381
[GenBank]
), forward, 5'-TCACAAAAGCCACTCCACTG-3', reverse, 5'-CATCTCAGAAGCGATCGTCA-3'; cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4) (Cdkn2c) (GenBank accession number NM_131902
[GenBank]
), forward, 5'-ACCGAACTGGTTTTGCTGTC-3', reverse, 5'-GGGCAGGTTCCCTTCATTAT-3'; and ubiquitin-activating enzyme E1 (GenBank accession number XM_217252
[GenBank]
), forward, 5'-ACAATTGGCCCAGCTTAATG-3', reverse, 5'-CTTGGAGTCAGTCAGCACCA-3'. No other products were amplified because melting curves showed only one peak in each primer pair. Fluorescence signals were measured over 40 PCR cycles. The cycle number (Ct) at which the signals crossed a threshold set within the logarithmic phase was recorded. For quantitation, we evaluated the difference in cycle threshold ( Ct) between the AP-treated group and vehicle control of each gene. The efficiency of amplification of each pair of primers was determined by serial dilutions of templates and all were >0.9. Each sample was normalized with the loading references -actin and GAPDH. Ct values used were the means of triplicate replicates. Experiments were repeated at least three times.
Western blot analyses for CDC2 and PCNA protein expression. The effects of AP on gene expression were further validated at the protein level by Western blot analyses. AP was added to the cultures after a 1 h seeding period, and cells were lysed at the time points as indicated. Cells were washed with cold PBS and incubated in ice-cold lysis buffer consisting of 0.1% SDS, 1% Igepal CA-630 (nonionic, nondenaturing detergent), 0.2 mM phenylmethylsulfonylfluoride, and 0.01 protease inhibitor mixture (Sigma) for 30 min at 4°C. Cell lysates were centrifuged at 12,000 x g for 10 min, and the concentration of protein in the supernatant was determined by the BCA protein assay (Sigma). Twenty micrograms of total protein from whole-cell lysates were separated under reducing and denaturing conditions by 12% SDS-PAGE and electro-transferred to a polyvinylidene difluoride membrane (Millipore). Nonspecific binding sites were blocked with 5% skim milk in PBS containing 0.05% Tween 20 (PBS-Tween). A purified rabbit IgG recognizing the C-terminal domain of CDC2/p34 (ab7953; Novus Biologicals, Littleton, CO), a cell-proliferation marker (Gannon et al., 1998), was used to evaluate regulation of CDC2 expression. Mouse IgG2a (clone PC10; Zymed Laboratories, San Francisco, CA) directed to PCNA, a commonly used marker of cell proliferation (Gannon et al., 1998), was used to evaluate the cell proliferation. The membranes were incubated with CDC2 antibody (1:500 in PBS-Tween/1% goat serum) or PCNA antibody (1:1000 in PBS-Tween/1% horse serum) overnight at 4°C. Membranes were then incubated in horseradish peroxidase-conjugated goat anti-rabbit or horse anti-mouse IgG (1:6000), and results were visualized by the TMB Peroxidase Substrate kit (Vector Laboratories). Relative amounts of CDC2 and PCNA were quantified by optical density analysis using the UN-SCAN-IT gel automated digitizing system (Scion, Frederick, MD). The level was normalized with respect to GAPDH, a domestic loading control. Data are presented as means ± SEM for at least three independent experiments.
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Figure 1. Characterization of neural progenitor cells in primary cultures of embryonic day 18 rat hippocampus. A, At 1 DIV, nestin (top)-positive cells are clustered, and nestin immunoreactivity is apparent within the cytoplasmic compartment of both the cell body and neurites. Nonclustered cells are nestin negative. The middle shows that the majority of cells are Tuj1 positive. The bottom shows one cell with BrdU immunoreactivity (green) localized to the nuclear compartment. Scale bars, 20 µm. B, At 1 DIV, a proportion of cells show coexpression of nestin (green) and MAP2 (red), as evidenced by yellow fluorescence. The majority of cells are MAP2 positive. At 4 DIV, the majority of cells label positive for MAP2, whereas immunolabeling for nestin, GFAP, and MBP is rarely observed. These data are consistent with the previous demonstration that the majority (>99%) of cells, under these culture conditions, are phenotypically neuronal (Brewer et al., 1993; Brewer, 1995). Scale bars, 20 µm.
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Statistical analyses. Differences in cell-proliferation markers were determined using one-way ANOVA, followed by a Neuman-Keuls post hoc analysis. Data derived from cDNA array or Western blot analyses represent semiquantitative estimates of the amount of a specific mRNA or protein that was present in a cell extract. The data displayed in graphs are reported as means ± SEM or fold change ± SEM of the actual scanning units derived from the densitometric analysis of each cDNA array or for Western blot densitometric units normalized to internal standard for protein content.
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Results
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Characterization of neuroprogenitor cells in primary cultures of embryonic day 18 rat hippocampal neurons
Dissociated cultures from E18 rat hippocampus were cultured in serum-free Neurobasal/B27 medium for 1-7 d. Immunochemical markers revealed that the cultures were predominantly neuronal in composition and also possessed a proportion of NPCs (Fig. 1A,B). Labeling for nestin, a large intermediate filament protein (class type VI) expressed during development and typically disappearing after E18, was used to identify progenitor cells (Fig. 1A, top) (Doetsch et al., 1997; Roy et al., 2000; Yamaguchi et al., 2000; Kawaguchi et al., 2001; Sawamoto et al., 2001; Romero-Ramos et al., 2002). Tuj1 labeling for neuron-specific III-microtubulin was conducted to identify cells committed to neuronal lineage (Fig. 1A, middle) (Menezes and Luskin, 1994; Menezes et al., 1995; Romero-Ramos et al., 2002). This antigen is not expressed by astrocytes or oligodendrocytes and is an early marker of neuronal differentiation for progenitor cells undergoing mitosis and for postmitotic neurons (Doetsch et al., 1997; Jacobs and Miller, 2000). Specific antibodies recognizing MAP2, a specific marker for postmitotic and differentiated neurons (Menezes and Luskin, 1994; Niijima et al., 1995; Young et al., 2000), GFAP, a specific marker for astrocytes, and MBP, a marker for oligodendrocytes, were also used. DAPI was used as a nuclear counterstain.
At 1 DIV, 27.4 ± 4.7% of cells were positive for nestin (Fig. 1A, top), 93 ± 6.3% of cells were positive for Tuj1 (Fig. 1A, middle), and 5.4% cells showed BrdU-positive nuclei (Fig. 1A, bottom), whereas at 7 DIV, no BrdU-positive nuclei were observed (data not shown). At 1 and 4 DIV, 96 ± 3.8 and 98 ± 1.6%, respectively, of the cells were positive for MAP2 (Fig. 1B). At 4 DIV, <2% of the cells were nestin positive, and <0.4% of the total cell population were GFAP and MBP positive. These results are consistent with previous reports indicating that neurons and their precursors make up the majority of postmitotic cultures and that glial cell contributions to the culture are reduced to <0.5% of the nearly pure neuronal population, as judged by immunocytochemistry for GFAP and neuron-specific enolase (Brewer et al., 1993; Brewer, 1995).
AP increases the number of nestin- and BrdU-positive cells
At 1 DIV, nestin-positive cells were found in clusters (as shown in Fig. 1A). In hippocampal cultures exposed to 500 nM AP, 36.3 ± 7.2% nestin-positive cells were observed compared with the 27.4 ± 4.7% observed in the control group, presenting a 32% increase in progenitor cells. This observation led us to perform a BrdU incorporation study to verify the proliferative effect of AP. Hippocampal neuron cultures were treated with either vehicle or 500 nM AP. Each set of cultures were exposed to BrdU (10 µM) for 4 h, followed by a 12 h of culture. Cultures treated with AP had a significantly greater number of BrdU-positive cells relative to vehicle control: 138 ± 10 (in every 2000 cells counted) vs 108 ± 6 (in every 2000 cells) (see Fig. 3B), which represents a 26% increase in BrdU-positive cells relative to control (Fig. 2).
Biphasic dose-response of AP-induced BrdU incorporation
The dose-response of AP-induced proliferation was determined by chemiluminescence BrdU cell-proliferation ELISA. Data from three independent assays conducted in octuplets are presented in Figure 3. As a positive control, hippocampal neurons were treated with EGF (20 ng/ml), which induced a 40 ± 9% increase in BrdU incorporation. Exposure of hippocampal neurons to different concentrations of AP for 1 DIV showed a biphasic regulation in BrdU incorporation. Exposure of hippocampal neurons to different concentrations of AP for 1 DIV revealed a dose-dependent biphasic regulation of BrdU incorporation. At 100, 250, and 500 nM concentrations, AP significantly increased BrdU incorporation (lower concentrations were not statistically different from control). At 1000 nM, a reversal of the dose-response was first apparent, with higher doses shifting the response to significant repression of proliferation at 100-1000 µM. Comparison of neurogenic efficacy indicated that AP was nearly as efficacious as the growth factor EGF.
AP promotes the proliferation of neural progenitor cells derived from E18 rat hippocampus
To quantitatively assess the neurogenic efficacy of AP by FACS, primary cultures of rat hippocampal neurons were infected with MuLV-eGFP virus in the presence or absence of AP or AP (serving as a negative control) 1 h after seeding for 4 h. The numbers of GFP-labeling dividing cells were measured by FACS at 2 DIV (Fig. 4A). In control cultures, 153 ± 12 per 2000 FACS sorted cells were positive for GFP. In cultures treated with 500 nM AP, 194 ± 17 per 2000 FACS sorted cells were positive (Table 1) and exhibited a 27% increase versus control (Fig. 4B). A slight but not statistically significant increase in GFP-positive cells was apparent in cultures treated with the stereoisomer AP: 163 ± 11 per 2000 FACS sorted cells (Table 1, Fig. 4B). The 27% increase in the number of GFP-positive neurons induced by AP determined by FACS analysis is consistent with the percentage increase in BrdU incorporation (24 ± 9% for 250 nM and 28 ± 8% at 500 nM) and the total cell number determined by a nonfluorescent automatic cell counter, as shown in Figure 4C, in which a 28 ± 6 and 32 ± 12% increase in total cells was observed for 250 nM and 500 nM AP-treated groups, respectively, compared with the vehicle control group. These data are also consistent with the results derived from the nestin expression analyses, which showed a 32% increase in nestin-positive cells.
Under fluorescent microscopy, the morphology of GFP-positive cells exhibited features of typical neurons, which were comparable with GFP-negative neurons (Fig. 4D), with a prominent nucleus and neurite extensions (Fig. 4E). GFP-positive cells also expressed positive Tuj1 immunoreactivity, indicating that these cells were of a neuronal lineage.
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Figure 4. AP increases the proliferation of GFP-labeled hippocampal neural progenitor cells and the total number of cells. Cultures were treated with vehicle, 500 nM AP, or 500 AP in the presence of MuLV-GFP retroviral particles (2 x 106/ml) for 4 h and further incubated with AP, AP, or vehicle in the absence of MuLV-GFP retroviral particles for 44-48 h. A, FACS profile. Area E presents the MuLV-GFP fluorescent cells, and area D presents the nonfluorescent cells. Results of FACS analysis indicated a greater number of cells sorted to the E fluorescent region. B, The relative percentage of positive MuLV-GFP cells was plotted and shows that AP induced a 27% increase in the number of FACS sorted GFP-labeled neural progenitor cells, which was significantly increased above control and AP conditions. The stereoisomer AP was without effect on GFP incorporation into hippocampal neural progenitor cells. C, Ratio of the total number of cells determined by particle size analyzer set to detect particles of 12-25 µm. Date derived from analysis of vehicle condition were set to 1, and data from other conditions are plotted relative to a vehicle value of 1. Analysis of total number of cells revealed that both 250 and 500 nM AP induced a significant increase in the number of cells. Data were derived from three independent experiments, analyzed by one-way ANOVA, followed by Neuman-Keuls post hoc analysis, and are presented as mean ± SEM. D, Fluorescent microscopy images of MuLV-GFP-labeled cells. Each panel of D shows the fluorescent image overlaid onto the differential interference contrast image to visualize the underlying cells. Scale bar, 20 µm. E, Coimmunolabeling of GFP-positive cells with the neuron-specific marker Tuj1 (red). Cells that coexpress GFP and Tuj1 appear yellow and label those cells that have divided and express a neuron-specific phenotype. Nuclei were counterstained with DAPI (blue). Scale bar, 20 µm.
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Validation of the MuLV-eGFP retrovirus as a strategy to determine neuron proliferation
To verify the accuracy of this strategy for neurogenesis determinations in primary hippocampal neurons, we executed FACS analyses in a constantly dividing hippocampal cell line, the mouse clonal HT-22 cell line, as a positive control. At 2 DIV after infection, 25-32% cells (449-638 per 2000 cells) were positive for GFP (Table 2), which is consistent with the one cell cycle per day mitotic rate for HT-22 cells (Sagara et al., 2002; Mize et al., 2003) and indicates that infection by MuLV-eGFP did not promote nor interfere with mitosis.
When HT-22 cells were treated with 500 nM AP, the number of GFP-positive cells increased to 680 ± 32 per 2000 FACS sorted cells, an increase of 22% over control condition (558 ± 28) for this continually dividing cell line at 2 DIV (Table 2, Fig. 5A). GFP-positive cells exhibited typical HT-22 cell morphology and GFP subcellular location (Fig. 5B). As a negative control, rat hippocampal neurons at 7 DIV treated with the same amount of viral loading showed no GFP-positive cells (data not shown), which is consistent with the BrdU incorporation results showing no BrdU incorporation in rat hippocampal cultures after 7 DIV.
Neurogenic effect of AP is stereospecific
To determine the steroid specificity for induction of neurogenesis, uptake of [3H]thymidine incorporation was used as a surrogate marker of DNA synthesis and mitosis. Results (Fig. 6) of these analyses indicate that 250 nM AP induced a highly significant increase (150 ± 21%) in [3H]thymidine incorporation relative to the control. Progesterone induced a 126 ± 12% increase (p < 0.05 vs control). Although the percentage average of progesterone was lower than that of AP, there was no statistical difference between them (p > 0.05) in [3H]thymidine incorporation. However, the stereoisomers of AP, i.e., epiallopregnanolone and AP, as well as 5-pregnan-3-ol were without effect. Additionally, allopregnandiol, 5-pregnan-3, 17, 20-triol, and pregnenolone sulfate, which we demonstrated to increase neurites number and length of primary cultured rat hippocampal neurons (our unpublished data), induced a significant decrease in [3H]thymidine incorporation, which is consistent with their differentiation effect. The steroid specificity analysis provides evidence for both the specificity of AP-induced mitogenesis and supportive evidence that factors that promote morphological differentiation, such as pregnenolone sulfate, have an effect opposite to that of AP in primary cultured rat hippocampal progenitor cells.
AP treatment regulates gene expression for cell-cycle proteins
The mitogenic action of AP predicted the regulation of cell-cycle gene expression. To determine AP regulation of cell-cycle gene expression, we used a biased DNA gene array containing genes known to control cell proliferation. Primary cultures of rat hippocampal neurons were treated with 500 nM AP, which resulted in a marked upregulation of the genes that promotes the cell cycle, such as an eightfold increase in cyclin E, a protein that promotes progression from G1 to S phase, a fourfold increase in two members of the M phase promoting factor complex, CDC2 (also called CDK1) and cyclin B, which promotes M phase transition required for completion of mitosis. In addition, another well defined cell-proliferation marker (Gannon et al., 1998; Graeber et al., 1998), PCNA, showed a more than twofold increase in expression. In contrast to the increase in cell-cycle genes involved in progression through the cell cycle, the expression of cell-cycle inhibitors CDK4 and CDK6, inhibitors p16 and p18, were decreased by more than twofold (Fig. 7A).
Because multiple endpoints were measured, there was an increased probability that differences in gene expression could occur by chance alone. To address this issue, the gene expression data were divided into subgroups of genes known to promote or inhibit cell proliferation, and the data from each subgroup of genes were subjected to multivariate ANOVA (Snedecor and Cochran, 1967; Jiang et al., 2002). Results of this analysis indicated a statistically significant effect of AP treatment on cyclins, CDKs, and CDK inhibitors (Table 3).
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Figure 6. The neurogenic property of AP is specific and not shared by isomers or other steroids in the biosynthetic pathway. Rat hippocampal neurons were loaded with 1 µCi/ml [3H]thymidine in the presence or absence of the indicated neurosteroids at 37°C for 24 h. AP induced a 150% increase in [3H]thymidine incorporation relative to control. Moreover, DNA synthesis was specific to AP compared with other structurally and chemically similar steroids. P4, the precursor molecule to AP, also induced a modest increase in [3H]thymidine incorporation; however, the stereoisomers of allopregnanolone, epiallopregnanolone, and AP, as well as 5-pregnan-3-ol, were without effect. Additionally, allopregnanediol, allopregnantriol, and pregnenolone sulfate induced a significant decrease in [3H]thymidine incorporation. Data are expressed as mean ± SEM. *p < 0.05; **p < 0.01; ***p < 0.001.
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As validation of the gene-array data, real-time PCR was performed for five mRNAs coding for genes that promote transition through the cell cycle, two genes that inhibit cell-cycle progression, and two invariant genes. As presented in Figure 7B, 500 nM AP increased the mRNA expression: 9.61 ± 0.8-fold for cyclin E versus control; 5.76 ± 0.56 for cyclin B; 4.24 ± 0.51 for CDC2; and 6.35 ± 0.3 for PCNA. In addition, cyclin A2, an S phase expression protein, increased 4.35 ± 0.34-fold. In contrast, AP treatment decreased the mRNA expression of Cdkn2c (p18) 4.84 ± 0.32-fold and ubiquitin-activating enzyme E1 4.16 ± 0.4-fold versus control. These results are entirely consistent with the direction of change indicated by the gene-array data, although the real-time PCR data indicate a slightly greater magnitude of fold change. Together, these data indicate that AP promotes the expression of activators of cell-cycle progression, such as cyclins, CDKs, and PCNA, while simultaneously downregulating the CDK inhibitors and other ubiquitin-related genes.
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Figure 7. AP regulates cell-cycle gene expression. Cultures of hippocampal neurons were treated with vehicle or 500 nM AP for 24 h, followed by extraction of total RNA. A, Gene array of cell-cycle-related gene expression. Nonradioactive probes were prepared and hybridized to a 96-gene miniarray. Two housekeeping genes (-actin and GAPDH) were used as internal controls. Two blanks and pUC18 from bacterial plasmid were used as negative controls. Data were represented as fold change of mRNA expression in AP-treated neurons versus control (mean ± SEM) as determined by optical density. Results of these analyses in cultured hippocampal neurons indicate that AP induced a marked increase in genes that promote progression through the cell cycle while inhibiting genes associated with exiting the cell cycle. AP induced an eightfold increase in cyclin E, which promotes progression from G1 to S phase, and a more than twofold increase in two well defined cell proliferation markers, CDC2 (also known as CDK1) and PCNA. In parallel to an increase in cell-cycle progression genes, AP inhibited the expression of CDK4 and CDK6 inhibitors and ubiquitin and cullin 3, which are associated with exiting the cell cycle. Two housekeeping genes, actin and GAPDH, were unchanged. Data were from three separate experiments, and multivariant ANOVA statistical analysis indicated that the increase and decrease were statistically significant, as presented in Table 3. B, Validation of the gene-array results by real-time RT-PCR. AP induced a significant increase in mRNA expression of cyclin A2, cyclin B1, cyclin E, CDC2, and PCNA mRNA, whereas AP induced a significant reduction in mRNA for cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4) and ubiquitin-activating enzyme E1 (Ube1X). These quantitative PCR data are entirely consistent with the gene-array results. Data are depicted as fold change of mRNA expression in AP-treated neurons versus vehicle control (mean ± SEM) from three separate experiments. Controls were set to zero. *p < 0.05.
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AP increases the protein level of cell-proliferating markers CDC2 and PCNA
Based on the results of the gene-array analysis, two well defined cell-proliferating markers, CDC2 and PNCA, were further analyzed by Western blot to determine whether increases in mRNA for mitotic cell-cycle genes were indicative of increases in protein. Whole-cell lysates from hippocampal neurons treated with 500 nM AP and control neurons were assessed by Western blot for CDC2 and PNCA. As shown in Figure 8, A and B, both CDC2 and PNCA protein levels were elevated by 1.5- or 2-fold by AP. These results indicate that AP significantly increased protein expression for two cell-cycle proteins, CDC2 and PCNA, which are required for progression through mitosis. These data are consistent with the mRNA increases observed in the cell-cycle gene expression analysis.
Antagonist to VGLCC abolishes AP-induced neuronal cell proliferation
Based on previous findings from our group that demonstrated that AP induced a significant rise in intracellular calcium in cultured hippocampal neurons during 1-10 d in vitro that was dependent on the GABAAR and the VGLCC (Son et al., 2002), we determined whether the neurogenic effect of AP was antagonized by the VGLCC blocker nifedipine. Nifedipine alone had no effect on rat hippocampal primary culture proliferation, whereas nifedipine completely abolished 500 nM AP-induced NPC proliferation increase (Fig. 9). These results indicate that AP requires activation of the VGLCC to promote neurogenesis.
AP induces proliferation of human neural stem cells from the cerebral cortex
To determine whether our findings in rat neural progenitor cells were relevant to proliferation of human neural stem cells, we investigated the neurogenic properties of AP in human neural stem cells derived from the human cerebral cortex (Jakel et al., 2004; Suzuki et al., 2004). Results of those analyses indicate that AP induced a highly significant increase in BrdU incorporation (35 ± 10 to 49 ± 15% increase vs control in the range of 1-500 nM AP). As with the rNPCs, AP-induced neurogenesis in the hNSCs was dose dependent and exhibited a biphasic response. AP was a more potent neurogenic factor in the hNSCs with a minimally effective dose of 1 nM, whereas in the rNPCs the minimally effective dose was 100 nM. The efficacy of AP as a neurogenic factor in hNSCs was comparable with that induced by bFGF (20 ng/ml) plus heparin (5 µg/ml) treatment (30 ± 9% increase vs control) (Fig. 10A). The stem cell marker nestin (Fig. 10B) and the neural progenitor marker Tuj1 (Fig. 10C) were both expressed in the human neural stem cells.
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Discussion
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In this study, we demonstrated that AP specifically increased proliferation of rat hippocampal NPCs and human cerebral cortical NSCs in a dose-dependent manner. In parallel, AP significantly increased expression of genes that promote progression through the cell cycle while inhibiting expression of genes involved in cell-cycle repression. Immunocytochemical labeling for NPC markers indicated that the newly formed cells are of neuronal lineage. Furthermore, we determined that the mechanism for AP-induced neurogenesis requires activation of VGLCCs.
Potency and efficacy of AP-induced neurogenesis
AP-induced neurogenesis was a dose-dependent process, with concentrations within the 10-9 to mid 10-7 M range promoting proliferation, whereas concentrations in excess of 10-6 M significantly inhibiting neurogenesis. The biphasic effect of AP on neurogenesis is supported by a recent study showing that nanomolar levels of AP increase whereas micromolar levels of AP inhibit the proliferation of polysialylated form of the neural cell adhesion molecule (PSA-NCAM)-positive neural progenitors (Gago et al., 2004). At high concentrations (i.e., in micromolar), AP can be converted by 20 hydroxysteroid dehydrogenase to allopregnanediol (Wiebe and Lewis, 2003) and hence may increase the local concentration of allopregnanediol that inhibited DNA replication of rNPC, thereby inducing a biphasic dose-response.
AP was a more potent neurogenic factor for hNSCs with a minimally effective dose of 1 nM, whereas in the rNPCs the minimally effective dose was >10 nM. The concentrations of AP required to induce neurogenesis in vitro are comparable with those found in both rat and human brain. AP levels are 12 ng/g (38 nM) in the pregnant maternal rat brain and 19 ng/g (60 nM) within the embryonic rat brain (Concas et al., 1998; Grobin and Morrow, 2001). In the human premenopausal female, AP levels in serum are 4 nM in the middle of menstrual cycle (Wang et al., 1996; Genazzani et al., 1998) and are 160 nM during the third trimester in healthy pregnant women (Luisi et al., 2000). Because a similar concentration has been detected in the umbilical cord, it is suggested to be an indicator of fetal levels of AP (Luisi et al., 2000).
In contrast to fetal development, an age-associated decrease in serum AP was observed in men >40 yr of age but remarkably not in women (Genazzani et al., 1998). Interestingly, a significant decrease (approximately threefold) in AP levels was observed in patients with Alzheimer's disease compared with the age-matched control group (Bernardi et al., 2000; Weill-Engerer et al., 2002). In parallel, in the aged brain, both the pool of NSC and their proliferative potential are markedly diminished (Jin et al., 2003; Wise, 2003; Enwere et al., 2004).
Reported herein, AP-induced neurogenesis ranged from 20 to 30% in the rodent NPCs to 37-49% in the human neural stem cells. The efficacy of AP as a neurogenic factor is comparable with that induced by bFGF plus heparin from our own study and also in agreement with previously published results. For example, bFGF induced a 0.4-fold increase in cultured rat brain-derived progenitor cells (Gago et al., 2003) after 3 d treatment and a 25% increase in BrdU incorporation in 3-month-old rat brain (Jin et al., 2003). Additional support comes from the recent studies that AP induces an 20% increase in thymidine incorporation in immatured rat cerebral granular cells (Keller et al., 2004) and a 20-30% increase in PSA-NCAM-positive progenitor proliferation derived from rat brain (Gago et al., 2004). Together, these data indicate that AP can promote neurogenesis of neural stem cells derived from multiple sites within the rodent brain and from the cerebral cortex of human brain.
Genetic and proliferative properties of AP-induced neurogenesis
The gene-array and real-time RT-PCR data are consistent with a neurogenic effect of AP. Genes that promote transition through the cell cycle and proliferation, such as cyclins and CDKs, including CDC2, cyclin B, and PNCA, were upregulated by AP. Correspondingly, AP downregulated the expression of genes involved in inhibition and degradation of CDKs and cyclins, such as CDK4 and CDK6 inhibitor p16, p18, cullin 3, and ubiquitin-activating enzyme E1, enzymes that are required for ubiquitination of mitotic cyclins and promote exit from the cell cycle (Schulman et al., 2000; Tyers and Jorgensen, 2000). In our study, AP not only regulated the expression of cell-cycle proteins and DNA amplification but also drove a complete mitosis of the rNPCs. This conclusion is supported by the data showing that AP increases the MuLV-GFP-positive cell number, because GFP signal can only be observed in the cells that transversed a complete cell cycle (Roe et al., 1993; Lewis and Emerman, 1994; Bieniasz et al., 1995). Moreover, the AP |
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Abstract
Introduction
