Newey Sarah E, Velamoor Vanisree, Govek Eve-Ellen, Van Aelst Linda
Cold Spring Harbor Laboratory, New York 11724, USA.
J Neurobiol. 2005 Jul;64(1):58-74. doi: 10.1002/neu.20153.
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.
智力迟钝患者神经元的一个一致特征是树突结构异常和/或树突棘形态改变。树突细胞骨架调节缺陷会影响树突和突触的结构与功能,在某些情况下被认为是智力迟钝的基础。支持这一观点的是,有充分证据表明,涉及小GTP酶Rho家族(肌动蛋白和微管细胞骨架的关键调节因子)的信号通路改变,会导致综合征性和非综合征性智力迟钝障碍。由于Rho GTP酶在决定树突和树突棘的发育及形态方面所起的作用越来越明确,有人提出Rho信号对正常认知很重要。本综述的目的是总结有关Rho GTP酶在树突和树突棘形态发生方面的最新数据,并强调它们在这些分子的调节因子和效应器内各种基因突变导致的智力迟钝中的作用。