Rho GTPases, dendritic structure, and mental retardation

被引:284
作者
Newey, SE [1 ]
Velamoor, V [1 ]
Govek, EE [1 ]
Van Aelst, L [1 ]
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
来源
JOURNAL OF NEUROBIOLOGY | 2005年 / 64卷 / 01期
基金
英国惠康基金;
关键词
dendrites; spines; mental retardation; Rho GTPases; actin; cytoskeleton;
D O I
10.1002/neu.20153
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A consistent feature of neurons in patients with mental retardation is abnormal dendritic structure and/or alterations in dendritic spine morphology. Deficits in the regulation of the dendritic cytoskeleton affect both the structure and function of dendrites and synapses and are believed to underlie mental retardation in some instances. In support of this, there is good evidence that alterations in signaling pathways involving the Rho family of small GTPases, key regulators of the actin and microtubule cytoskeletons, contribute to both syndromic and nonsyndromic mental retardation disorders. Because the Rho GTPases have been shown to play increasingly well-defined roles in determining dendrite and dendritic spine development and morphology, Rho signaling has been suggested to be important for normal cognition. The purpose of this review is to summarize recent data on the Rho GTPases pertaining to dendrite and dendritic spine morphogenesis, as well as to highlight their involvement in mental retardation resulting from a variety of genetic mutations within regulators and effectors of these molecules. (c) 2005 Wiley periodicals, Inc.
引用
收藏
页码:58 / 74
页数:17
相关论文
共 191 条
[1]   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
[2]   ADP-ribosylation factor 6 and a functional PIX/p95-APP1 complex are required for Rac1B-mediated neurite outgrowth [J].
Albertinazzi, C ;
Za, L ;
Paris, S ;
de Curtis, I .
MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (04) :1295-1307
[3]   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
[4]   Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase [J].
Arber, S ;
Barbayannis, FA ;
Hanser, H ;
Schneider, C ;
Stanyon, CA ;
Bernard, O ;
Caroni, P .
NATURE, 1998, 393 (6687) :805-809
[5]   THE LOWE OCULOCEREBRORENAL SYNDROME GENE ENCODES A PROTEIN HIGHLY HOMOLOGOUS TO INOSITOL POLYPHOSPHATE-5-PHOSPHATASE [J].
ATTREE, O ;
OLIVOS, IM ;
OKABE, I ;
BAILEY, LC ;
NELSON, DL ;
LEWIS, RA ;
MCINNES, RR ;
NUSSBAUM, RL .
NATURE, 1992, 358 (6383) :239-242
[6]   A tyrosine-phosphorylated protein that binds to an important regulatory region on the cool family of p21-activated kinase-binding proteins [J].
Bagrodia, S ;
Bailey, D ;
Lenard, Z ;
Hart, M ;
Guan, JL ;
Premont, RT ;
Taylor, SJ ;
Cerione, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (32) :22393-22400
[7]   Understanding fragile X syndrome: insights from animal models [J].
Bakker, CE ;
Oostra, BA .
CYTOGENETIC AND GENOME RESEARCH, 2003, 100 (1-4) :111-123
[8]   Signals from the X: signal transduction and X-linked mental retardation [J].
Barnes, AP ;
Milgram, SL .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2002, 20 (3-5) :397-406
[9]   The mGIuR theory of fragile X mental retardation [J].
Bear, MF ;
Huber, KM ;
Warren, ST .
TRENDS IN NEUROSCIENCES, 2004, 27 (07) :370-377
[10]   DENDRITIC ATROPHY IN CHILDREN WITH DOWNS-SYNDROME [J].
BECKER, LE ;
ARMSTRONG, DL ;
CHAN, F .
ANNALS OF NEUROLOGY, 1986, 20 (04) :520-526