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Previous Article | Next Article
The Journal of Neuroscience, November 1, 2001, 21(21):8426-8434
Distinct Roles for the Two Rho GDP/GTP Exchange Factor Domains of Kalirin in Regulation of Neurite Growth and Neuronal Morphology
Peter Penzes1, Richard C. Johnson1, Vikram Kambampati1, Richard E. Mains2, and Betty A. Eipper2 1 Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, and 2 Department of Neuroscience, University of Connecticut Health Center, Farmington, Connecticut 06030
ABSTRACT
TOP
ABSTRACT
INTRODUCTION
The actin cytoskeleton, essential for neuronal development, is regulated in part by small GTP binding proteins of the Rho subfamily. Kalirin-9, with two Rho subfamily-specific GDP/GTP exchange factor (GEF) domains, localizes to neurites and growth cones of primary cortical neurons. Kalirin-9 overexpression in cultured cortical neurons induces longer neurites and altered neuronal morphology. Expression of the first GEF domain alone results in drastically shortened axons and excessive growth cones, mediated by Rac1. Expression of the second GEF domain alone induces axonal over-elongation and abundant filopodial neurites, mediated by RhoA. Coordination of the actions of the individual GEF domains through their presence in Kalirin-9, with its Sec14p, spectrin, and Src homology domain 3 motifs, is essential for regulating neurite extension and neuronal morphology.
Key words: Rac1; RhoA; Trio; spectrin; cytoskeleton; growth cone
INTRODUCTION
The actin cytoskeleton plays an essential role in morphological changes during neuronal development and plasticity. Rho GTPases are key regulators of the actin cytoskeleton (Hall, 1998
), and there is ample evidence involving Rho GTPases in growth of neurites and axon guidance (Luo et al., 1994
Tremendous progress has been made in uncovering extracellular signals and the receptors that regulate neurite outgrowth and growth cone guidance (Tessier-Lavigne and Goodman, 1996
Kalirin, a Dbl family member with multiple isoforms, is highly expressed in adult rat CNS (Alam et al., 1997
Studies in Drosophila and C. elegans indicate that a protein homologous to Kalirin-9 (dTrio and UNC-73, respectively) is an essential player in multiple axon guidance pathways (Steven et al., 1998
MATERIALS AND METHODS
DNA and antibodies. Rac1-N17 and RhoA-N19 plasmids were gifts from Dr. Silvio Gutkind (National Institute of Dental Research, National Institutes of Health, Bethesda, MD), whereas glutathione S-transferase (GST)-RhoA, GST-Rac1, and GST-Cdc42 plasmids and constitutively active Rac1 (Rac1-Q61L) and RhoA (RhoA-Q63L) plasmids were gifts from Dr. Richard Cerione (Cornell University, Ithaca, NY). Rabbit polyclonal antisera against regions of Kalirin were affinity purified (Johnson et al., 2000
Cell cultures and transient transfections. NIH3T3 cells were cultured in DMEM-F-12 containing 10% fetal bovine serum (HyClone, Logan, UT) and 10% NuSerum (Collaborative Research, Bedford, MA). For immunocytochemistry, cells grown on glass chamber slides for 3 d to 40-60% confluence were transfected with 1 µg of plasmid DNA per 4 cm2 of pEAK10.His-Myc-DHPH1, pEAK10.His-Myc-DHPH2, or pEAK10.His-Myc-Kal-9 and 4 µl of Lipofectamine (Life Technologies, Gaithersburg, MD) in 1 ml of complete serum-free medium for 5 hr, after which they were washed and fed with growth medium. After 1 d, medium was replaced with DMEM-F-12 for 16 hr. Cells fixed in 3.7% formaldehyde in PBS (50 mM NaPi, pH7.5, and 150 mM NaCl) for 30 min at room temperature were permeabilized and stained.
Neuronal cultures and transfections. Rat embryo cerebral cortex (embryonic day 18) digested with papain for 30 min at 37°C was dissociated by pipetting. Neurons were plated in chamber slides precoated with poly-L-lysine in MEM containing 2 mM glutamine and 5% heat-inactivated horse serum (Life Technologies), penicillin, and streptomycin. After 2 d at 37°C in 5% CO2, cultures were transfected using the calcium phosphate method for 15 min (Penzes et al., 2001
Rac1 GTPase activation assays. Activation of Rac1 was measured with the Rac1/Cdc42 activation assay kit (Upstate Biotechnology). Briefly, cells that had been transfected 1 d earlier were serum-starved overnight, and cell lysates (~0.5 mg of protein) were incubated for 1 hr at 4°C with 10 µl of GST-PAK1-PBD resin per sample. Bound proteins were eluted and analyzed by SDS-PAGE and Western blotting with Rac1 and Cdc42 monoclonal antibodies.
DHPH binding to Rho GTPases. The GST fusion proteins of Rho GTPases purified from Escherichia coli were depleted of bound nucleotide by incubation in 10 mM EDTA. pEAK-rapid human embryonic kidney 293 (HEK-293) cells expressing myc-DHPH1 or myc DHPH2 were extracted in binding buffer (20 mM Tris-HCl, pH 7.5, and 50 mM NaCl containing 1% Triton X-100). For each binding reaction, 5 µg of GST-GTPase bound to 25 µl of glutathione-Sepharose beads was mixed with an aliquot of cell extract containing 1 mg of protein for 1 hr at 4°C. The beads were washed three times with binding buffer, and bound proteins eluted with Laemmli's buffer were analyzed by SDS-PAGE and Western blotting using the monoclonal myc antibody.
Tissue preparation and subcellular fractionation. Parietal cortex dissected from Sprague Dawley (Harlan Sprague Dawley, Indianapolis, IN) rat pups was sonicated in 10 vol of buffer A: 20 mM Tris HCl, pH 7.5, 1% SDS, 0.3 mg/ml PMSF, 50 µg/ml lima bean trypsin inhibitor, 2 µg/ml leupeptin, 16 µg/ml benzamidine, and 2 µg/ml pepstatin. Cultured primary neurons were extracted in the same buffer. Samples were prepared by addition of 2 vol of 1× SDS-PAGE loading buffer and analyzed by SDS-PAGE and Western blotting.
RESULTS
Expression of Kalirin isoforms with single and dual DHPH domains
To determine when Kalirin isoforms with single or dual DHPH domains are expressed, we used a Kalirin antibody directed to the common spectrin-like domains to evaluate expression during postnatal development (Fig. 1b). Forms with two DHPH domains, Kalirin-9 and Kalirin-12, are prevalent at postnatal day 2 (P2), a time when they could play a role in neural development. Expression of Kalirin-7, with a single DHPH domain, is not detectable until 2 weeks after birth, with increasing levels thereafter, consistent with its reported function in generation of spine-like structures in mature hippocampal neurons (Penzes et al., 2001
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Figure 1. Expression of Kalirin. a, Kalirin isoforms and related proteins. Bars indicate antigens used to generate antibodies. b, Expression of Kalirin in rat cerebral cortex (25 µg of protein) during postnatal development, detected with the Kal-spec antibody (1:1000). c, Expression of Kalirin isoforms in 4-d-old cultures of dissociated cortical neurons (25 µg of protein), detected with the indicated Kalirin antibodies. Kal-spec was used at 1:1000; Kalirin-9, Kalirin-12, and Kalirin-7 affinity-purified antibodies were used at 1:100. Kalirin-7 cannot be detected at this age. FnIII, Fibronectin III; div, days in vitro.
Because we wanted to use cultured neurons to study the function of Kalirin and its isolated DHPH domains, we evaluated extracts of 4-d-old dissociated cortical cultures using several Kalirin antibodies (Fig. 1c). The expression patterns of Kalirin isoforms in primary cortical cultures and P2 brain extracts are similar; forms of Kalirin with two DHPH domains predominate, and Kalirin-7 is not detectable (Fig. 1c).
Kalirin is a dual-function GEF
The first DHPH domain of Kalirin (DHPH1) is similar to the first DHPH domain of Trio (Debant et al., 1996
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Figure 2. Biochemical characterization of Kalirin. a, Binding of the individual DHPH domains of Kalirin to nucleotide-depleted Rho GTPases. myc-DHPH1 and myc-DHPH2 were expressed in pEAK-rapid HEK-293 cells, and lysates (1 mg of protein) were incubated with 5 µg of GST or nucleotide-depleted GST-RhoA, GST-Rac1, or GST-Cdc42. Bound proteins were analyzed by Western blotting with the myc monoclonal antibody. Bound GST fusion proteins were visualized with Coomassie blue (bottom). b, GTPase activation by DHPH1 and DHPH2. DHPH1 and DHPH2 were transiently expressed in pEAK-rapid HEK-293 cells. Six hours after transfection, cells were serum starved for 15 hr. Activation of endogenous GTPases was measured by evaluating their binding to GST-PAK1-PBD. Bound GTPases were detected by Western blotting (top). Expression of the DHPH protein was detected by Western blotting with the myc antibody (bottom). c, Effects of transient expression of myc-DHPH1, myc-DHPH2, and myc-Kalirin-9 on cellular morphology and filamentous actin in NIH3T3 fibroblasts. Scale bar, 20 µm. R, Ruffles; nt, nontransfected cells; sf, stress fibers. d, Expression of Rac1 and RhoA in P2 rat cerebral cortex (20 µg of protein).
Because both DHPH1 and DHPH2 bound nucleotide-depleted Rac1, we examined the activation of Rac1 and Cdc42 by DHPH1 and DHPH2. We expressed myc-tagged DHPH1 or DHPH2 in pEAK-rapid HEK-293 cells and measured the activation of endogenous Rac1 (Fig. 2b) and Cdc42 (data not shown) by affinity isolation of their activated forms. Expression of the DHPH1 domain resulted in activation of Rac1 but not Cdc42. On the contrary, expression of DHPH2 at the same level activated neither Rac1 nor Cdc42. As for DHPH2, other Dbl family members have been found to bind to Rho family members without catalyzing nucleotide exchange (Whitehead et al., 1997
We used fibroblasts to compare the actions of the isolated DHPH domains of Kalirin with those of full-length Kalirin-9 (Fig. 2c). We transfected fibroblasts with myc-tagged Kalirin constructs. After serum starvation, we detected expression of the Kalirin proteins by immunostaining for the myc tag and examined the actin cytoskeleton by staining with FITC-phalloidin. As reported, DHPH1-transfected cells are disc shaped and display lamellipodia and ruffles, indicative of activated Rac1 (Hall, 1998
Full-length Kalirin-9, which includes both DHPH domains, induced a phenotype distinct from that of either DHPH domain alone. The formation of both lamellipodia and stress fibers was increased when Kalirin-9 was transfected into fibroblasts. Cells expressing Kalirin-9 did not exhibit the massive ruffles seen in cells expressing DHPH1, suggesting that the DHPH1 domain may not be as active when part of the larger protein. This experiment suggests that both DHPH domains are activated to some extent in serum-starved fibroblasts.
To evaluate the expression of the potential Kalirin substrates in cortical cultures and to test the specificities of the commercial monoclonal antibodies for Rac1 and RhoA, we probed Western blots with monoclonal antibodies specific for Rac1 and RhoA (Fig. 2d). Both Rho proteins were readily detected, with both antibodies visualizing doublets of ~21 kDa proteins, showing that the antibodies are specific.
Kalirin forms are compartmentalized in neurons
To examine the distribution of endogenous Kalirin in cultured cortical neurons, we used form-specific Kalirin antisera and neuron-specific tubulin antiserum (Fig. 3a,b). We examined young (P0-P2) neurons and found that essentially all of the neurons expressed both Kalirin-9 and Kalirin-12. Whereas endogenous Kalirin-9 was abundant in processes, along with the cell soma (Fig. 3a), endogenous Kalirin-12 was exclusively localized to the cell soma (Fig. 3b). Staining of neurons with Kalirin-9 antibodies along with the dendritic marker microtubule-associated protein 2 (MAP2) or the axonal marker tau showed that Kalirin-9 was abundant in both dendrites and axons (Fig. 3c,d). Depletion of both antisera by binding to affinity resins containing the corresponding antigenic peptide confirmed that the antibodies detected the desired epitopes (Fig. 3e). Because the two dual DHPH domain forms of Kalirin are localized differently, each may play a distinct role in regulating neuronal process growth.
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Figure 3. Compartmentalization of endogenous Kalirin. Cultured cortical neurons (2 d in vitro) were stained simultaneously for neuron-specific tubulin (nst) (a, b) and Kalirin-9 (a) or Kalirin-12 (b), MAP2 and Kalirin-9 (c), and tau and Kalirin-9 (d). e, Immunostaining with Kalirin-9 and Kalirin-12 antibody solutions depleted by binding to antigen-affinity resins. f, Immunostaining of cultured neurons with Kal-spec antibody. Simultaneous immunostaining of cultured neurons for Kal-spec and F-actin (g), Rac1 (h), or RhoA (i). Scale bars: a-f, 20 µm; g-i, 5 µm. p, Processes; s, soma; a, axons; d, dendrites; gc, growth cones; arrowheads, growth cone filopodia.
Because the Kalirin-9 antibody showed several cross-reactive bands on Western blots, we corroborated these observations by immunostaining cultures with the Kalirin
spectrin (Kal-spec) antibody (Fig. 3f). Kalirin was visualized in growth cones (gc) and in the perinuclear region of the cell soma (s). Kalirin was abundant in the growth cones (Fig. 3g-i, arrowheads), in which it colocalized with filamentous actin (F-actin) (Fig. 3g). Rac1 and RhoA, potential Kalirin substrates, are also localized to growth cones (Fig. 3h,i). Because Kalirin-12 is primarily localized to the cell soma (Fig. 3b) and Western blot analysis indicates that Kalirin-9 is the major isoform, growth cone staining is likely to represent Kalirin-9. Thus, Kalirin-9 is located where it could regulate actin assembly via available Rho protein substrates.
Kalirin-9 and its individual DHPH domains have different effects on neuronal process length and morphology
Based on the function of invertebrate proteins related to Kalirin and the striking subcellular localization of Kalirin in neurites and growth cones, we first compared the ability of Kalirin-9 and its individual DHPH domains to affect neurite extension. We expressed green fluorescent protein (GFP) (control) (Fig. 4a) and myc-tagged Kalirin-9 (Fig. 4b) in young cortical neurons (P0). We evaluated the effect of overexpressing myc-Kalirin-9 by measuring the length of the longest process in the population of neurons visualized with the myc antibody. The longest processes in myc-Kalirin-9-expressing neurons were significantly longer than the longest processes of control neurons expressing GFP alone; GFP was visualized by autofluorescence (Fig. 4c).
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Figure 4. Overexpression of Kalirin-9 and its individual DHPH domains affects length of neurites. Cortical neurons (2 d in vitro) were transfected with GFP (a) or myc-Kalirin-9 (b). Scale bar, 10 µm. c, The length of the longest process in each Kalirin-9- or GFP-expressing neuron was determined. Low-magnification pictures of cortical cultures transfected with myc-DHPH1 (d), myc-DHPH2 (e), or GFP (f). Scale bar, 100 µm. g, Histograms of lengths of the longest process of transfected neurons. For c and g, error bars are SDs for three experiments, each containing 40-80 neurons. Cultured cortical neurons transfected with myc-DHPH1 (h, i, left) or myc-DHPH2 (h, i, right) were stained for myc and MAP2 (h) or myc and tau (i). Scale bar, 20 µm.
To evaluate the contribution of the individual DHPH domains to the function of Kalirin-9, we overexpressed each DHPH domain in young cortical neurons (Fig. 4d,e). Expression of DHPH1 resulted in neurons with significantly shorter processes (Fig. 4d,g, top) than control neurons (Fig. 4c, top, f). In contrast, expression of DHPH2 (Fig. 4e,g, bottom) resulted in a larger number of neurons with much longer processes than control neurons, Kalirin-9-transfected neurons, or neurons expressing DHPH1. For neurons transfected with myc-tagged DHPH1 or DHPH2, myc staining filled dendrites to the same extent as MAP2 staining and axons to the same extent as tau staining. Based on staining intensity, the expression levels of transfected DHPH1 and DHPH2 were similar.
To determine whether the processes affected by overexpression of the DHPH domains were axons or dendrites, we stained transfected neurons with the dendritic marker MAP2 (Fig. 4h, arrow d) or with the axonal marker tau (Fig. 4i, arrow a). Some of the longest processes of neurons transfected with DHPH1 stained with the MAP2 antibody, whereas others stained with the tau antibody (Fig. 4h,i), showing that expression of DHPH1 affected the length of both types of processes. In contrast, the longest processes of DHPH2-transfected neurons stained for tau but not for MAP2, indicating that they were axons (Fig. 4h,i). Thus, expression of the individual DHPH domains of Kalirin affected the growth of axons in opposite ways: DHPH1 expression resulted in a drastic reduction in length or disappearance of the axon, whereas DHPH2 expression induced an exaggerated extension of the axon.
Other morphological alterations were apparent after expression of Kalirin-9, DHPH1, and DHPH2 in cortical neurons. Neurons overexpressing Kalirin-9 often displayed multiple lateral growth cones extending from neurites (Fig. 5a). A large fraction of neurons overexpressing Kalirin-9 had growth cones on their cell soma. An even larger fraction of neurons expressing DHPH1 had growth cones on their cell body (Fig. 5b, inset, gc; quantified in e); neurons expressing DHPH2 (Fig. 5c) or GFP (Fig. 5d) did not exhibit a similar morphology. DHPH1-expressing neurons, although they had been in culture for 4 d, were reminiscent of the first stages of emergence of neurites.
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Figure 5. Expression of Kalirin-9 and its DHPH domains affects the morphology of cortical neurons. Morphological features induced by overexpression of Kalirin-9 (a), DHPH1 (b), DHPH2 (c), and GFP (d). Scale bars: a, 10 µm; b-d, 20 µm. gc, Growth cones; s, soma; fn, aberrant filopodial neurites. e, Percentage of neurons with one or more growth cones on soma. f, Percentage of neurons with abundant aberrant filopodial neurites extending from the soma. Bars represent averages of values for ~50 neurons, in three separate experiments; error bars are SDs. Cells were visualized by immunostaining with antisera for myc (a-c) or by GFP autofluorescence (d) cones on soma. f, Percentage of neurons with abundant aberrant filopodial neurites extending from the soma. Bars represent averages of values for ~50 neurons, in three separate experiments; error bars are SDs. Cells were visualized by immunostaining with antisera for myc (a-c) or by GFP autofluorescence (d).
Neurons expressing DHPH2 had many small aberrant filopodial neurites (fn) and shorter and thinner than normal processes, densely covering the soma (Fig. 5c, inset; quantified in f), dendrites, and axon. Such structures were much less abundant on neurons expressing GFP, DHPH1, or Kalirin-9. Localization of endogenous Kalirin-9 to growth cones and small neuritic filopodia along processes places it at the sites of action of its overexpressed DHPH domains. These observations suggest that endogenous Kalirin-9 may generate these structures by selective activation of its DHPH1 and DHPH2 domains.
DHPH1 and DHPH2 actions involve Rac1 and RhoA, respectively
To determine whether the effects of DHPH1 and DHPH2 on neurons involve the small GTPases Rac1 and RhoA, we used dominant negative constructs of Rac1 and RhoA (Ridley and Hall, 1992
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Figure 6. The actions of Kalirin-9 and its DHPH domains involve Rac1 and RhoA. a, Coexpression of dominant negative Rac1 and RhoA. Histogram of lengths of longest processes of neurons cotransfected with DHPH1 plus Rac1-T17N or DHPH2 plus RhoA-T19N. Bars represent averages of >30 neurons in each experiment, and error bars are SDs for two experiments. b, Histogram of lengths of longest processes of neurons expressing dominant negative Rac1-N17 and RhoA-N19 in the absence of exogenous Kalirin. Morphology of neurons transfected with DHPH2 plus C3 transferase (c), Kalirin-9 plus Rac1-T17N (d), or Kalirin-9 plus RhoA-T19N (e). Histograms of lengths of longest processes of neurons cotransfected with DHPH2 plus C3 transferase (f), Kalirin-9 plus Rac1-T17N (g, top), or Kalirin-9 plus RhoA-T19N (g, bottom). Bars represent averages of >30 neurons in each experiment, and error bars are SDs for two experiments.
Our results regarding the effects of Rac1 and RhoA on neurite outgrowth in cortical cultures were not those predicted based on some previous studies (van Leeuwen et al., 1997
To confirm that DHPH2 action involved activation of RhoA, we cotransfected neurons with vectors encoding myc-DHPH2 and C3 enzyme, a Clostridium botulinum ADP-ribosyltransferase that ADP-ribosylates Rho proteins and inactivates RhoA (Aktories et al., 1987
To examine the behavior of the two DHPH domains in the context of full-length Kalirin-9, we cotransfected neurons with Kalirin-9 along with Rac1-T17N or RhoA-T19N, respectively. Overexpression of Kalirin-9 with Rac1-T17N resulted in neurons with cell bodies covered with small filopodial neurites (Fig. 6d,f), similar to those of neurons overexpressing DHPH2. The longest processes of these neurons were slightly longer than those of neurons overexpressing Kalirin-9 alone (Figs. 4c, 6g, top). Thus, the effects of Kalirin-9 on cortical neurons are mediated in part through activation of Rac1.
A considerable fraction of the neurons overexpressing Kalirin-9 and RhoA-T19N displayed massive lamellipodia on their soma and lateral growth cones along their neurites, reminiscent of the phenotype of neurons overexpressing DHPH1 (Fig. 6e). Overexpression of Kalirin-9 with RhoA-T19N resulted in neurons with slightly shorter processes than those of neurons expressing Kalirin-9 alone (Fig. 6g, bottom). Thus, the effects of Kalirin-9 are mediated in part through activation of RhoA. These results are consistent with the behavior of Kalirin-9 and its separate DHPH domains when transfected into NIH3T3 fibroblasts (Fig. 2c). Dominant negative Rac and Rho exerted a greater effect on neurons overexpressing Kalirin-9 than on control neurons (Fig. 6b, g); this may reflect the more controlled activation of endogenous Kalirin or the involvement of additional factors. Together, these experiments demonstrate that both DHPH domains are active in the context of the full-length protein. Protein localization or controlled activation of individual DHPH domains within the context of the full-length protein may account for the distinct effects of Kalirin-9.
DISCUSSION
An important role for dual DHPH isoforms of Kalirin in neurite growth in cortical neurons is supported by several lines of evidence. In the neonatal rat cortex, expression of Kalirin-9 and Kalirin-12 predominates, with little expression of Kalirin-7. Kalirin-9 is enriched in processes and growth cones of cortical neurons, with a striking localization to zones of intense growth. The dramatic effects of Kalirin-9 and its isolated DHPH1 and DHPH2 domains on neurite length and neuronal morphology implicate this protein in neuritogenesis, a process that takes place at the sites of localization of endogenous Kalirin-9. The homology of Kalirin-9 with Drosophila Trio and C. elegans UNC-73A, both involved in axon growth and guidance, implicates Kalirin in similar processes.
Whereas invertebrates have a single Kalirin/Trio gene, mammals have two, as revealed by database searches. In both Drosophila and C. elegans, Trio plays essential roles both within and outside the nervous system (Awasaki et al., 2000
In Drosophila and C. elegans, expression of the dual DHPH proteins dTrio and Unc-73 is essential for axon growth and guidance (Steven et al., 1998
Neurons encounter spatial issues not faced by other cells. One way they could address these problems is by using dual-function GEFs such as Kalirin-9 and Kalirin-12 to coordinate the actions of individual GEF activities. The actions of full-length Kalirin-9 are not simply the sum of the actions of its individual DHPH domains. The presence of two distinct GEF activities in a single protein, such as Kalirin-9, allows coordinated regulation of the morphological changes induced; this may be especially important for neurite extension versus retraction. In the context of the full-length Kalirin protein, both DHPH domains are active in neonatal cortical neurons. Neither domain appears to be maximally activated under control conditions, making it possible for each domain to be activated in a regulated manner. Extracellular attractive or repulsive cues may selectively activate one DHPH domain or the other, and Kalirin-9 may have its separate DHPH domains activated like a switch, to quickly respond to the growth needs of the neuron, by virtue of its localization to active zones of growth.
The actions of DHPH1 and DHPH2 in neonatal cortical neurons are different, more dramatic and more complex than those reported for Rac1 and RhoA alone. These differences may reflect localization of the DHPH proteins or their ability to interact with multiple Rho proteins. The ability of DHPH domains to bind Rho proteins without activating them can clearly play a role in the differences observed. Diverse effects of Rho GTPases on neuronal morphology have been reported previously (Luo et al., 1994
The effect of any DHPH domain will depend on the complement of Rho proteins present in any given neuron at a particular time. In addition, the action of a particular Rho family member may vary with cell type and developmental stage. For example, C. elegans UNC-73B and Drosophila Still life (SIF) both activate Rac1, yet UNC-73 stimulates axon growth and SIF inhibits it (Sone et al., 1997
FOOTNOTES Received June 19, 2001; revised Aug. 1, 2001; accepted Aug. 7, 2001.
This work was supported by National Institutes of Health Grants DA-00266 and DK-32948. We thank Dr. L. Redmond for her help with neuronal transfections. We thank Drs. A. Ghosh, A. Kolodkin, and C. Hopf for their useful advice and for critically reading this manuscript.
Correspondence should be addressed to Betty A. Eipper, Department of Neuroscience, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030. E-mail: eipper{at}uchc.edu.
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