Axon Branching Requires Interactions between Dynamic Microtubules and Actin Filaments

Cortical neurons innervate many of their targets by collateral axon branching, which requires local reorganization of the cytoskeleton. We coinjected cortical neurons with fluorescently labeled tubulin and phalloidin and used fluorescence time-lapse imaging to analyze interactions between microtubules and actin filaments (F-actin) in cortical growth cones and axons undergoing branching. In growth cones and at axon branch points, splaying of looped or bundled microtubules is accompanied by focal accumulation of F-actin. Dynamic microtubules colocalize with F-actin in transition regions of growth cones and at axon branch points. In contrast, F-actin is excluded from the central region of the growth cone and the axon shaft, which contains stable microtubules. Interactions between dynamic microtubules and dynamic actin filaments involve their coordinated polymerization and depolymerization. Application of drugs that attenuate either microtubule or F-actin dynamics also inhibits polymerization of the other cytoskeletal element. Importantly, inhibition of microtubule or F-actin dynamics prevents axon branching but not axon elongation. However, these treatments do cause undirected axon outgrowth. These results suggest that interactions between dynamic microtubules and actin filaments are required for axon branching and directed axon outgrowth.

[1]  D. Bentley,et al.  Accumulation of actin in subsets of pioneer growth cone filopodia in response to neural and epithelial guidance cues in situ , 1993, The Journal of cell biology.

[2]  P. Forscher,et al.  Cytoskeletal remodeling during growth cone-target interactions , 1993, The Journal of cell biology.

[3]  P. J. Smith,et al.  Birefringence imaging directly reveals architectural dynamics of filamentous actin in living growth cones. , 1999, Molecular biology of the cell.

[4]  P. Gordon-Weeks Evidence for microtubule capture by filopodial actin filaments in growth cones. , 1991, Neuroreport.

[5]  M. Kirschner,et al.  Microtubule behavior in the growth cones of living neurons during axon elongation , 1991, The Journal of cell biology.

[6]  A. Desai,et al.  Fluorescent speckle microscopy, a method to visualize the dynamics of protein assemblies in living cells , 1998, Current Biology.

[7]  A. Mikhailov,et al.  Relationship between microtubule dynamics and lamellipodium formation revealed by direct imaging of microtubules in cells treated with nocodazole or taxol. , 1998, Cell motility and the cytoskeleton.

[8]  K. Kalil,et al.  Interstitial Branches Develop from Active Regions of the Axon Demarcated by the Primary Growth Cone during Pausing Behaviors , 1998, The Journal of Neuroscience.

[9]  P Wadsworth,et al.  Nanomolar concentrations of nocodazole alter microtubule dynamic instability in vivo and in vitro. , 1997, Molecular biology of the cell.

[10]  J. Challacombe,et al.  Actin filament bundles are required for microtubule reorientation during growth cone turning to avoid an inhibitory guidance cue. , 1996, Journal of cell science.

[11]  Lorene M Lanier,et al.  From Abl to actin: Abl tyrosine kinase and associated proteins in growth cone motility , 2000, Current Opinion in Neurobiology.

[12]  F. Braet,et al.  New anti‐actin drugs in the study of the organization and function of the actin cytoskeleton , 1999, Microscopy research and technique.

[13]  K. Kalil,et al.  Dynamic behaviors of growth cones extending in the corpus callosum of living cortical brain slices observed with video microscopy , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  T. J. Keating,et al.  Microtubule release from the centrosome. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[15]  J. Bamburg,et al.  Rac1-dependent actin filament organization in growth cones is necessary for beta1-integrin-mediated advance but not for growth on poly-D-lysine. , 1998, Journal of neurobiology.

[16]  D. O'Leary,et al.  Target selection by cortical axons: alternative mechanisms to establish axonal connections in the developing brain. , 1990, Cold Spring Harbor symposia on quantitative biology.

[17]  David Pellman,et al.  Microtubule “Plus-End-Tracking Proteins” The End Is Just the Beginning , 2001, Cell.

[18]  G. Gallo,et al.  Localized Sources of Neurotrophins Initiate Axon Collateral Sprouting , 1998, The Journal of Neuroscience.

[19]  D. Drubin,et al.  Functional cooperation between the microtubule and actin cytoskeletons. , 2000, Current opinion in cell biology.

[20]  H. Ris,et al.  Novel organization of microtubules in cultured central nervous system neurons: formation of hairpin loops at ends of maturing neurites , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  A. Hyman,et al.  Preparation of modified tubulins. , 1991, Methods in enzymology.

[22]  E. Salmon,et al.  Microtubules Remodel Actomyosin Networks in Xenopus Egg Extracts via Two Mechanisms of F-Actin Transport , 2000, The Journal of cell biology.

[23]  E. Tanaka,et al.  Making the connection: Cytoskeletal rearrangements during growth cone guidance , 1995, Cell.

[24]  M. Kirschner,et al.  The role of microtubule dynamics in growth cone motility and axonal growth , 1995, The Journal of cell biology.

[25]  D. Lübbers,et al.  Heterogeneity and stability of local PO2 distribution within the brain tissue. , 1994, Advances in experimental medicine and biology.

[26]  S. J. Smith,et al.  Actions of cytochalasins on the organization of actin filaments and microtubules in a neuronal growth cone , 1988, The Journal of cell biology.

[27]  M. Kirschner,et al.  Dynamic instability of microtubule growth , 1984, Nature.

[28]  P. Forscher,et al.  The Ig Superfamily Cell Adhesion Molecule, apCAM, Mediates Growth Cone Steering by Substrate–Cytoskeletal Coupling , 1998, The Journal of cell biology.

[29]  R. J. Finst,et al.  Direct observation of microtubule-f-actin interaction in cell free lysates. , 1999, Journal of cell science.

[30]  P. Forscher,et al.  Substrate-cytoskeletal coupling as a mechanism for the regulation of growth cone motility and guidance. , 2000, Journal of neurobiology.

[31]  E. Salmon,et al.  Microtubule growth activates Rac1 to promote lamellipodial protrusion in fibroblasts , 1999, Nature Cell Biology.

[32]  E. Dent,et al.  GAP-43 phosphorylation is dynamically regulated in individual growth cones. , 1992, Journal of neurobiology.

[33]  C. Goodman,et al.  Profilin and the Abl Tyrosine Kinase Are Required for Motor Axon Outgrowth in the Drosophila Embryo , 1999, Neuron.

[34]  P Wadsworth,et al.  Taxol suppresses dynamics of individual microtubules in living human tumor cells. , 1999, Molecular biology of the cell.

[35]  M. Black,et al.  Individual microtubules in the axon consist of domains that differ in both composition and stability , 1990, The Journal of cell biology.

[36]  W. Sossin,et al.  Protein Kinase C Activation Promotes Microtubule Advance in Neuronal Growth Cones by Increasing Average Microtubule Growth Lifetimes , 2001, The Journal of cell biology.

[37]  W. Kiosses,et al.  Regulation of the small GTP‐binding protein Rho by cell adhesion and the cytoskeleton , 1999, The EMBO journal.

[38]  D. Nelson,et al.  Cdc42-interacting Protein 4 Mediates Binding of the Wiskott-Aldrich Syndrome Protein to Microtubules* , 2000, The Journal of Biological Chemistry.

[39]  Y. Li,et al.  Composite microtubules of the axon: quantitative analysis of tyrosinated and acetylated tubulin along individual axonal microtubules. , 1993, Journal of cell science.

[40]  F. McNally Cytoskeleton: CLASPing the end to the edge , 2001, Current Biology.

[41]  J. Bamburg,et al.  Cdc42 stimulates neurite outgrowth and formation of growth cone filopodia and lamellipodia. , 2000, Journal of neurobiology.

[42]  E. Salmon,et al.  Positive feedback interactions between microtubule and actin dynamics during cell motility. , 1999, Current opinion in cell biology.

[43]  P. Forscher,et al.  Cytoskeletal reorganization underlying growth cone motility , 1995, Current Opinion in Neurobiology.

[44]  K. Kalil,et al.  Common mechanisms underlying growth cone guidance and axon branching. , 2000, Journal of neurobiology.

[45]  G. Gallo,et al.  Different Contributions of Microtubule Dynamics and Transport to the Growth of Axons and Collateral Sprouts , 1999, The Journal of Neuroscience.

[46]  Chad W. Seys,et al.  Fibroblast Growth Factor-2 Promotes Axon Branching of Cortical Neurons by Influencing Morphology and Behavior of the Primary Growth Cone , 2001, The Journal of Neuroscience.

[47]  T. Mitchison,et al.  Regulated Actin Cytoskeleton Assembly at Filopodium Tips Controls Their Extension and Retraction , 1999, The Journal of cell biology.

[48]  P. Bridgman,et al.  Nerve growth cone lamellipodia contain two populations of actin filaments that differ in organization and polarity , 1992, The Journal of cell biology.

[49]  P. Forscher,et al.  Growth cone advance is inversely proportional to retrograde F-actin flow , 1995, Neuron.

[50]  J Waters,et al.  A high-resolution multimode digital microscope system. , 1998, Methods in cell biology.

[51]  E. Salmon,et al.  Endoplasmic reticulum membrane tubules are distributed by microtubules in living cells using three distinct mechanisms , 1998, Current Biology.

[52]  M. Kirschner,et al.  Microtubule behavior during guidance of pioneer neuron growth cones in situ , 1991, The Journal of cell biology.

[53]  T. Mitchison,et al.  Microtubule polymerization dynamics. , 1997, Annual review of cell and developmental biology.

[54]  C. Cohan,et al.  Actin dynamics and organization during growth cone morphogenesis in Helisoma neurons. , 1997, Cell motility and the cytoskeleton.

[55]  G. Kreitzer,et al.  A signal transduction pathway involved in microtubule‐mediated cell polarization , 1999, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[56]  M. Schachner,et al.  Microtubule reorganization is obligatory for growth cone turning. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[57]  M. Dailey,et al.  The organization of myosin and actin in rapid frozen nerve growth cones , 1989, The Journal of cell biology.

[58]  K. Kalil,et al.  Reorganization and Movement of Microtubules in Axonal Growth Cones and Developing Interstitial Branches , 1999, The Journal of Neuroscience.

[59]  M. Dailey,et al.  Polymerizing microtubules activate site-directed F-actin assembly in nerve growth cones. , 1999, Molecular biology of the cell.

[60]  M. Dailey,et al.  Structure and organization of membrane organelles along distal microtubule segments in growth cones , 1991, Journal of neuroscience research.

[61]  G. Davis,et al.  Drosophila Futsch Regulates Synaptic Microtubule Organization and Is Necessary for Synaptic Growth , 2000, Neuron.

[62]  M. Rochlin,et al.  Microtubule Stability Decreases Axon Elongation but Not Axoplasm Production , 1996, The Journal of Neuroscience.

[63]  Y. Li,et al.  Microtubule assembly and turnover in growing axons , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[64]  Y. Wang,et al.  Assembly of actin-containing cortex occurs at distal regions of growing neurites in PC12 cells. , 1991, Journal of cell science.

[65]  J. Challacombe,et al.  Dynamic Microtubule Ends Are Required for Growth Cone Turning to Avoid an Inhibitory Guidance Cue , 1997, The Journal of Neuroscience.

[66]  D. Bentley,et al.  Cytoskeletal events in growth cone steering , 1994, Current Opinion in Neurobiology.