How do dendrites take their shape? (original) (raw)
Cajal, S. R. Histology of the Nervous System of Man and Vertebrates (Oxford Univ. Press, Oxford, 1995). Google Scholar
Hausser, M., Spruston, N. & Stuart, G. J. Diversity and dynamics of dendritic signaling. Science290, 739–744 (2000). ArticleCASPubMed Google Scholar
Cowan, W. M. The emergence of modern neuroanatomy and developmental neurobiology. Neuron20, 413–426 (1998). ArticleCASPubMed Google Scholar
Lo, D. C., McAllister, A. K. & Katz, L. C. Neuronal transfection in brain slices using particle-mediated gene transfer. Neuron13, 1263–1268 (1994). ArticleCASPubMed Google Scholar
Arnold, D., Feng, L., Kim, J. & Heintz, N. A strategy for the analysis of gene expression during neural development. Proc. Natl. Acad. Sci. USA91, 9970–9974 (1994). ArticleCASPubMedPubMed Central Google Scholar
Wu, G.-Y. & Cline, H. T. Stablization of dendritic arbor structure in vivo by CaMKII. Science279, 222–226 (1998). ArticleCASPubMed Google Scholar
Gao, F. B., Brenman, J. E., Jan, L. Y. & Jan, Y. N. Genes regulating dendritic outgrowth, branching, and routing in Drosophila. Genes Dev.13, 2549–2561 (1999). ArticleCASPubMedPubMed Central Google Scholar
Lee, T. & Luo, L. Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis. Neuron22, 451–461 (1999). ArticleCASPubMed Google Scholar
Banker, G. A. & Cowan, W. M. Further observations on hippocampal neurons in dispersed cell culture. J. Comp. Neurol.187, 469–493 (1979). ArticleCASPubMed Google Scholar
Polleux, F., Morrow, T. & Ghosh, A. Semaphorin 3A is a chemoattractant for cortical apical dendrites. Nature404, 567–573 (2000). ArticleCASPubMed Google Scholar
Wässle, H., Peichl, L. & Boycott, B. B. Dendritic territories of cat reginal ganglion cells. Nature292, 344–345 (1981). ArticlePubMed Google Scholar
Bradke, F. & Dotti, C. G. Establishment of neuronal polarity: lessons from cultured hippocampal neurons. Curr. Opin. Neurobiol.10, 574–581 (2000). ArticleCASPubMed Google Scholar
Lüscher, C., Nicoll, R. A., Malenka, R. C. & Muller, D. Synaptic plasticity and dynamic modulation of the postsynpatic membrane. Nat. Neurosci.3, 545–550 (2000). ArticlePubMed Google Scholar
Jontes, J. D. & Smith, S. J. Filopodia, spines and the generation of synpatic diversity. Neuron27, 11–14 (2000). ArticleCASPubMed Google Scholar
McAllister, A. K. Cellular and molecular mechanisms of dendrite growth. Cereb. Cortex10, 963–973 (2000). ArticleCASPubMed Google Scholar
Nedivi, E., Wu, G. Y. & Cline, H. T. Promotion of dendritic growth by CPG15, an activity-induced signaling molecule. Science281, 1863–1866 (1998). ArticleCASPubMedPubMed Central Google Scholar
Lein, P., Johnson, M., Guo, X., Rueger, D. & Higgins, D. Osteogenic protein-1 induces dendritic growth in rat sympathetic neurons. Neuron15, 597–605 (1995). ArticleCASPubMed Google Scholar
McAllister, A. K., Lo, D. C. & Katz, L. C. Neurotrophins regulate dendritic growth in developing visual cortex. Neuron15, 791–803 (1995). ArticleCASPubMed Google Scholar
McAllister, A. K., Katz, L. C. & Lo, D. C. Neurotrophin regulation of cortical dendritic growth requires activity. Neuron17, 1057–1064 (1996). ArticleCASPubMed Google Scholar
Horch, H. W., Kruttgen, A., Portbury, S. D. & Katz, L. C. Destabilization of cortical dendrites and spines by BDNF. Neuron23, 353–364 (1999). ArticleCASPubMed Google Scholar
Barbacid, M. Neurotrophic factors and their receptors. Curr. Opin. Cell Biol.7, 148–155 (1995). ArticleCASPubMed Google Scholar
McAllister, A. K., Katz, L. C. & Lo, D. C. Opposing roles for endogenous BDNF and NT-3 in regulating cortical dendritic growth. Neuron18, 767–778 (1997). ArticleCASPubMed Google Scholar
Fryer, R. H. et al. Developmental and mature expression of full-length and truncated TrkB receptors in the rat forebrain. J. Comp. Neurol.374, 21–40 (1996). ArticleCASPubMed Google Scholar
Yacoubian, T. A. & Lo, D. C. Truncated and full-length TrkB receptors regulate distinct modes of dendritic growth. Nat. Neurosci.3, 342–349 (2000). ArticleCASPubMed Google Scholar
Gundersen, R. W. & Barrett, J. N. Neuronal chemotaxis: chick dorsal-root axons turn toward high concentrations of nerve growth factor. Science206, 1079–1080 (1979). ArticleCASPubMed Google Scholar
Tessier-Lavigne, M. & Goodman, C. S. The molecular biology of axon guidance. Science274, 1123–1133 (1996). ArticleCASPubMed Google Scholar
Luo, Y., Raible, D. & Raper, J. A. Collapsin: a protein in brain that induces the collapse and paralysis of neuronal growth cones. Cell75, 217–227 (1993). ArticleCASPubMed Google Scholar
Messersmith, E. K. et al. Semaphorin III can function as a selective chemorepellent to pattern sensory projections in the spinal cord. Neuron14, 949–959 (1995). ArticleCASPubMed Google Scholar
Song, H. J. et al. Conversion of neuronal growth cone responses from repulsion to attraction by cyclic nucleotides. Science281, 1515–1518 (1998). ArticleCASPubMed Google Scholar
Giger, R. J., Wolfer, D. P., De Wit, G. M. & Verhaagen, J. Anatomy of rat semaphorin III/collapsin-1 mRNA expression and relationship to developing nerve tracts during neuroembryogenesis. J. Comp. Neurol.375, 378–392 (1996). ArticleCASPubMed Google Scholar
Polleux, F., Giger, R. J., Ginty, D. D., Kolodkin, A. L. & Ghosh, A. Patterning of cortical efferent projections by semaphorin-neuropilin interactions. Science282, 1904–1906 (1998). ArticleCASPubMed Google Scholar
Gertler, F. B. et al. enabled, a dosage-sensitive suppressor of mutations in the Drosophila Abl tyrosine kinase, encodes an Abl substrate with SH3 domain-binding properties. Genes Dev.9, 521–533 (1995). ArticleCASPubMed Google Scholar
Wills, Z., Bateman, J., Korey, K. A., Comer, A. & Van Vactor, D. The tyrosine kinase Abl and its substrate enabled collaborate with the receptor phosphatase Dlar to control motor axon guidance. Neuron22, 301–312 (1999). ArticleCASPubMed Google Scholar
Bashaw, G. J., Kidd, T., Murray, D., Pawson, T. & Goodman, C. S. Repulsive axon guidance: Abelson and Enabled play opposing roles downstream of the roundabout receptor. Cell101, 703–715 (2000). ArticleCASPubMed Google Scholar
Lanier, L. M. & Gertler, F. B. From Abl to actin: Abl tyrosine kinase and associated proteins in growth cone motility. Curr. Opin. Neurobiol.10, 80–87 (2000). ArticleCASPubMed Google Scholar
O'Leary, D. D. M. & Terashima, T. Cortical axons branch to multiple subcortical targets by interstitial axon budding: implications for target recognition and “waiting periods.” Neuron1, 901–910 (1988). ArticleCASPubMed Google Scholar
Yu, W., Ahmad, F. J. & Baas, P. W. Microtubule fragmentation and partitioning in the axon during collateral branch formation. J. Neurosci.14, 5872–5884 (1994). ArticleCASPubMedPubMed Central Google Scholar
Zakharenko, S. & Popov, S. Dynamics of axonal microtubules regulate the topology of new membrane insertion into the growing neurites. J. Cell Biol.16, 1077–1086 (1998). Article Google Scholar
Redmond, L. & Ghosh, A. The role of Notch and Rho GTPase signaling in the control of dendritic development. Curr. Opin. Neurobiol.11, 111–117 (2001). ArticleCASPubMed Google Scholar
Li, Z., Van Aelst, L. & Cline, H. T. Rho GTPases regulate distinct aspects of dendritic arbor growth in Xenopus central neurons in vivo. Nat. Neurosci.3, 217–225 (2000). ArticleCASPubMed Google Scholar
Wong, W. T., Faulkner-Jones, B., Sanes, J. R. & Wong, R. O. L. Rapid dendritic remodeling in the developing retina: dependence on neurotransmission and reciprocal regulation by Rac and Rho. J. Neurosci.20, 5024–5036 (2000). ArticleCASPubMedPubMed Central Google Scholar
Luo, L. et al. Differential effects of the Rac GTPase on Purkinje cell axons and dendritic trunks and spines. Nature379, 837–840 (1996). ArticleCASPubMed Google Scholar
Nakayama, A. Y., Harms, M. B. & Luo, L. Small GTPases Rac and Rho in the maintenance of dendritic spines and branches in hippocampal pyramidal neurons. J. Neurosci.20, 5329–5338 (2000). ArticleCASPubMedPubMed Central Google Scholar
Prokop, A., Uhler, J., Roote, J. & Bate, M. The kakapo mutation affects terminal arborization and central dendritic sprouting of Drosophila motorneurons. J. Cell Biol.143, 1283–1294 (1998). ArticleCASPubMedPubMed Central Google Scholar
Gregory, S. L. & Brown, N. H. Kakapo, a gene required for adhesion between and within cell layers in drosophila, encodes a large cytoskeletal linker protein related to plectin and dystrophin. J. Cell Biol.143, 1271–1282 (1998). ArticleCASPubMedPubMed Central Google Scholar
Strumpf, D. & Volk, T. Kakapo, a novel cytoskeletal-associated protein is essential for the restricted localization of the neuregulin-like factor, vein, at the muscle-tendon junction site. J. Cell Biol.143, 1259–1270 (1998). ArticleCASPubMedPubMed Central Google Scholar
Van Vactor, D., Sink, H., Fambrough, D., Tsoo, R. & Goodman, C. S. Genes that control neuromuscular specificity in Drosophila. Cell73, 1137–1153 (1993). ArticleCAS Google Scholar
Kolodziej, P. A., Jan, L. Y. & Jan, Y. N. Mutations that affect the length, fasciculation, or ventral orientation of specific sensory axons in the Drosophila embryo. Neuron15, 273–286 (1995). ArticleCASPubMed Google Scholar
Lee, S., Harris, K. L., Whitington, P. M. & Kolodziej, P. A. short stop is allelic to kakapo, and encodes rod-like cytoskeletal-associated proteins required for axon extension. J. Neurosci.20, 1096–1108 (2000). ArticleCASPubMedPubMed Central Google Scholar
Wang, K. H. et al. Biochemical purification of a mammalian slit protein as a positive regulator of sensory axon elongation and branching. Cell96, 771–784 (1999). ArticleCASPubMed Google Scholar
Gao, F. B., Kohwi, M., Brenman, J. E., Jan, L. Y. & Jan, Y. N. Control of dendritic field formation in Drosophila: the roles of flamingo and competition between homologous neurons. Neuron28, 91–101 (2000). ArticleCASPubMed Google Scholar
Usui, T. et al. Flamingo, a seven-pass transmembrane cadherin, regulates planar cell polarity under the control of Frizzled. Cell98, 585–595 (1999). ArticleCASPubMed Google Scholar
Ruchhoeft, M. L., Ohnuma, S., McNeill, L., Holt, C. E. & Harris, W. A. The neuronal architecture of Xenopus retinal ganglion cells is sculpted by rho-family GTPases in vivo. J. Neurosci.19, 8454–8463 (1999). ArticleCASPubMedPubMed Central Google Scholar
Lee, T., Winter, C., Marticke, S. S., Lee, A. & Luo, L. Essential roles of Drosophila RhoA in the regulation of neuroblast proliferation and dendritic but not axonal morphogenesis. Neuron25, 307–316 (2000). ArticleCASPubMed Google Scholar
Kimura, K. et al. Regulation of myosin phosphatase by Rho and Rho-associated kinase (Rho-kinase). Science273, 245–248 (1996). ArticleCASPubMed Google Scholar
Winter, C. G. et al. Drosophila Rho-associated kinase (Drok) links frizzled-mediated planar cell polarity signaling to the actin cytoskeleton. Cell (in press).
Hirose, M. et al. Molecular dissection of the Rho-associated protein kinase (p160ROCK)-regulated neurite remodeling in neuroblastoma N1E-115 cells. J. Cell Biol.141, 1625–1636 (1998). ArticleCASPubMedPubMed Central Google Scholar
Sestan, N., Artavanis-Tsakonas, S. & Rakic, P. Contact-dependent inhibition of cortical neurite growth mediated by notch signaling. Science286, 741–746 (1999). ArticleCASPubMed Google Scholar
Redmond, L., Oh, S., Hicks, C., Weinmaster, G. & Ghosh, A. Nuclear Notch1 signaling and the regulation of dendritic development. Nat. Neurosci.3, 30–40 (2000). ArticleCASPubMed Google Scholar
Altman, J. & Anderson, W. J. Experimental reorganization of the cerebellar cortex. I. Morphological effects of elimination of all microneurons with prolonged x-irradiation started at birth. J. Comp. Neurol.146, 355–406 (1972). ArticleCASPubMed Google Scholar
Rakic, P. & Sidman, R. L. Organization of cerebellar cortex secondary to deficit of granule cells in weaver mutant mice. J. Comp. Neurol.152, 133–162 (1973). ArticleCASPubMed Google Scholar
Baptista, C. A., Hatten, M. E., Blazeski, R. & Mason, C. A. Cell-cell interactions influence survival and differentiation of purified Purkinje cells in vitro. Neuron12, 243–260 (1994). ArticleCASPubMed Google Scholar
Segal, I., Korkotian, I. & Murphy, D. D. Dendritic spine formation and pruning: common cellular mechanisms? Trends Neurosci.23, 53–57 (2000). ArticleCASPubMed Google Scholar
Morrison, M. E. & Mason, C. A. Granule neuron regulation of Purkinje cell development: striking a balance between neurotrophin and glutamate signaling. J. Neurosci.18, 3563–3573 (1998). ArticleCASPubMedPubMed Central Google Scholar
Hirai, H. & Launey, T. The regulatory connection between the activity of granule cell NMDA receptors and dendritic differentiation of cerebellar Purkinje cells. J. Neurosci.20, 5217–5224 (2000). ArticleCASPubMedPubMed Central Google Scholar
Fischer, M., Kaech, S., Knutti, D. & Matus, A. Rapid actin-based plasticity in dendritic spines. Neuron20, 847–854 (1998). ArticleCASPubMed Google Scholar
Peters, A., Palay, S. L. & Webster, H. D. The Fine Structure of the Nervous System: Neurons and Their Supporting Cells (Oxford Univ. Press, New York, 1991). Google Scholar
Caceres, A., Mautino, J. & Kosik, K. S. Suppression of MAP2 in cultured cerebellar macroneurons inhibits minor neurite formation. Neuron9, 607–618 (1992). ArticleCASPubMed Google Scholar
Sharp, D. J. et al. Identification of a microtubule-associated motor protein essential for dendritic differentiation. J. Cell Biol.138, 833–843 (1997). ArticleCASPubMedPubMed Central Google Scholar
Yu, W. et al. Depletion of a microtubule-associated motor protein induces the loss of dendritic identity. J. Neurosci.20, 5782–5791 (2000). ArticleCASPubMedPubMed Central Google Scholar
Liu, Z., Steward, R. & Luo, L. Drosophila Lis1 is required for neuroblast proliferation, dendritic elaboration and axonal transport. Nat. Cell Biol.2, 776–783 (2000). ArticleCASPubMed Google Scholar
Smith, D. S. et al. Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1. Nat. Cell Biol.2, 767–775 (2000). ArticleCASPubMed Google Scholar
Niethammer, M. et al. Nudel is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein. Neuron28, 697–711 (2000). ArticleCASPubMed Google Scholar
Sasaki, S. et al. A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system. Neuron28, 681–696 (2000). ArticleCASPubMed Google Scholar
Nikolic, M., Chou, M. M., Lu, W., Mayer, B. J. & Tsai, L. H. The p35/Cdk5 kinase is a neuron-specific Rac effector that inhibits Pak1 activity. Nature395, 194–198 (1998). ArticleCASPubMed Google Scholar
Le Roux, P., Behar, S., Higgins, D. & Charette, M. OP-1 enhances dendritic growth from cerebral cortical neurons in vitro. Exp. Neurol.160, 151–163 (1999). ArticleCASPubMed Google Scholar
Cantallops, I., Haas, K. & Cline, H. T. Postsynaptic CPG15 promotes synaptic maturation and presynaptic axon arbor elaboration in vivo. Nat. Neurosci.3, 1004–1011 (2000). ArticleCASPubMed Google Scholar
Davies, A. M. Neurotrophins: neurotrophic modulation of neurite growth. Curr. Biol.10, R198–200 (2000). ArticleCASPubMed Google Scholar
Nakamura, F., Kalb, R. G. & Strittmatter, S. M. Molecular basis of semaphorin-mediated axon guidance. J. Neurobiol.44, 219–229 (2000). ArticleCASPubMed Google Scholar
Atwal, J. K., Massie, B., Miller, F. D. & Kaplan, D. R. The TrkB-Shc site signals neuronal survival and local axon growth via MEK and P13-kinase. Neuron27, 265–277 (2000). ArticleCASPubMed Google Scholar
Ichinose, T. & Snider, W. D. Differential effects of TrkC isoforms on sensory axon outgrowth. J. Neurosci. Res.59, 365–371 (2000). ArticleCASPubMed Google Scholar
Threadgill, R., Bobb, K. & Ghosh, A. Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42. Neuron19, 625–634 (1997). ArticleCASPubMed Google Scholar
Bito, H. et al. A critical role for a Rho-associated kinase, p160ROCK, in determining axon outgrowth in mammalian CNS neurons. Neuron26, 431–441 (2000). ArticleCASPubMed Google Scholar
Pfister, K. K. Cytoplasmic dynein and microtubule transport in the axon: the action connection. Mol. Neurobiol.20, 81–91 (2000). Article Google Scholar
Zou, D. J. & Cline, H. T. Postsynaptic calcium/calmodulin-dependent protein kinase II is required to limit elaboration of presynaptic and postsynaptic neuronal arbors. J. Neurosci.19, 8909–8918 (1999). ArticleCASPubMedPubMed Central Google Scholar
Gertler, F. B., Niebuhr, K., Reinhard, M., Wehland, J. & Soriano, P. Mena, a relative of VASP and Drosophila Enabled, is implicated in the control of microfilament dynamics. Cell87, 227–239 (1996). ArticleCASPubMed Google Scholar
Reinhard, M. et al. The proline-rich focal adhesion and microfilament protein VASP is a ligand for profilins. EMBO J.14, 1583–1589 (1995). ArticleCASPubMedPubMed Central Google Scholar
Vaessin, H. et al. prospero is expressed in neuronal precursors and encodes a nuclear protein that is involved in the control of axonal outgrowth in Drosophila. Cell67, 941–953 (1991). ArticleCASPubMed Google Scholar
Doe, C. Q., Chu-LaGraff, Q., Wright, D. M. & Scott, M. P. The prospero gene specifies cell fates in the Drosophila central nervous system. Cell65, 451–464 (1991). ArticleCASPubMed Google Scholar
Brand, A. H. & Perrimon, N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development118, 401–415 (1993). CASPubMed Google Scholar