The role of the Rho GTPases in neuronal development

被引:765
作者
Govek, EE
Newey, SE
Van Aelst, L
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] SUNY Stony Brook, Mol & Cellular Biol Program, Stony Brook, NY 11794 USA
关键词
Rho GTPases; neurite formation; axon formation; guidance; and regeneration; dendrite formation; spine morphogenesis; nervous system disorders;
D O I
10.1101/gad.1256405
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Our brain serves as a center for cognitive function and neurons within the brain relay and store information about our surroundings and experiences. Modulation of this complex neuronal circuitry allows us to process that information and respond appropriately. Proper development of neurons is therefore vital to the mental health of an individual, and perturbations in their signaling or morphology are likely to result in cognitive impairment. The development of a neuron requires a series of steps that begins with migration from its birth place and initiation of process outgrowth, and ultimately leads to differentiation and the formation of connections that allow it to communicate with appropriate targets. Over the past several years, it has become clear that the Rho family of GTPases and related molecules play an important role in various aspects of neuronal development, including neurite outgrowth and differentiation, axon pathfinding, and dendritic spine formation and maintenance. Given the importance of these molecules in these processes, it is therefore not surprising that mutations in genes encoding a number of regulators and effectors of the Rho GTPases have been associated with human neurological diseases. This review will focus on the role of the Rho GTPases and their associated signaling molecules throughout neuronal development and discuss how perturbations in Rho GTPase signaling may lead to cognitive disorders.
引用
收藏
页码:1 / 49
页数:49
相关论文
共 484 条
[1]   The insulin receptor tyrosine kinase substrate p58/53 and the insulin receptor are components of CNS synapses [J].
Abbott, MA ;
Wells, DG ;
Fallon, JR .
JOURNAL OF NEUROSCIENCE, 1999, 19 (17) :7300-7308
[2]   Small GTPase Tc10 and its homologue RhoT induce N-WASP-mediated long process formation and neurite outgrowth [J].
Abe, T ;
Kato, M ;
Miki, H ;
Takenawa, T ;
Endo, T .
JOURNAL OF CELL SCIENCE, 2003, 116 (01) :155-168
[3]   Activity-induced targeting of profilin and stabilization of dendritic spine morphology [J].
Ackermann, M ;
Matus, A .
NATURE NEUROSCIENCE, 2003, 6 (11) :1194-1200
[4]   Differential effects of Rho GTPases on axonal and dendritic development in hippocampal neurones [J].
Ahnert-Hilger, G ;
Höltje, M ;
Grosse, G ;
Pickert, G ;
Mucke, C ;
Nixdorf-Bergweiler, B ;
Boquet, P ;
Hofmann, F ;
Just, I .
JOURNAL OF NEUROCHEMISTRY, 2004, 90 (01) :9-18
[5]   Phosphorylation of cofilin by LIM-kinase is necessary for semaphorin 3A-induced growth cone collapse [J].
Aizawa, H ;
Wakatsuki, S ;
Ishii, A ;
Moriyama, K ;
Sasaki, Y ;
Ohashi, K ;
Sekine-Aizawa, Y ;
Sehara-Fujisawa, A ;
Mizuno, K ;
Goshima, Y ;
Yahara, I .
NATURE NEUROSCIENCE, 2001, 4 (04) :367-373
[6]   Overexpression of a neural-specific Rho family GTPase, cRac1B, selectively induces enhanced neuritogenesis and neurite branching in primary neurons [J].
Albertinazzi, C ;
Gilardelli, D ;
Paris, S ;
Longhi, R ;
de Curtis, I .
JOURNAL OF CELL BIOLOGY, 1998, 142 (03) :815-825
[7]   Identification of a carboxyl-terminal diaphanous-related formin homology protein autoregulatory domain [J].
Alberts, AS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (04) :2824-2830
[8]   Coordinating structural and functional synapse development: Postsynaptic p21-activated kinase independently specifies glutamate receptor abundance and postsynaptic morphology [J].
Albin, SD ;
Davis, GW .
JOURNAL OF NEUROSCIENCE, 2004, 24 (31) :6871-6879
[9]   PAK3 mutation in nonsyndromic X-linked mental retardation [J].
Allen, KM ;
Gleeson, JG ;
Bagrodia, S ;
Partington, MW ;
MacMillan, JC ;
Cerione, RA ;
Mulley, JC ;
Walsh, CA .
NATURE GENETICS, 1998, 20 (01) :25-30
[10]   A role for drosophila Drac1 in neurite outgrowth and synaptogenesis in the giant fiber system [J].
Allen, MJ ;
Shan, XL ;
Murphey, RK .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2000, 16 (06) :754-765