Boda Bernadett, Nikonenko Irina, Alberi Stefano, Muller Dominique
Department of Neuroscience, Centre Médical Universitaire, 1211 Geneva 4, Switzerland.
Mol Neurobiol. 2006 Aug;34(1):67-80. doi: 10.1385/mn:34:1:67.
Several of the genes currently known to be associated, when mutated, with mental retardation, code for molecules directly involved in Rho guanosine triphosphatase (GTPase) signaling. These include PAK3, a member of the PAK protein kinase family, which are important effectors of small GTPases. In many systems, PAK kinases play crucial roles regulating complex mechanisms such as cell migration, differentiation, or survival. Their precise functions in the central nervous system remain, however, unclear. Although their activity does not seem to be required for normal brain development, several recent studies point to a possible involvement in more subtle mechanisms such as neurite outgrowth, spine morphogenesis or synapse formation, and plasticity. This article reviews this information in the light of the current knowledge available on the molecular characteristics of the different members of this family and discuss the mechanisms through which they might contribute to cognitive functions.
目前已知有几个基因发生突变时与智力发育迟缓相关,它们编码的分子直接参与Rho鸟苷三磷酸酶(GTP酶)信号传导。这些基因包括PAK3,它是PAK蛋白激酶家族的成员,是小GTP酶的重要效应器。在许多系统中,PAK激酶在调节细胞迁移、分化或存活等复杂机制中发挥关键作用。然而,它们在中枢神经系统中的精确功能仍不清楚。虽然正常脑发育似乎不需要它们的活性,但最近的几项研究指出,它们可能参与了更细微的机制,如神经突生长、树突棘形态发生或突触形成以及可塑性。本文根据目前有关该家族不同成员分子特征的现有知识对这些信息进行综述,并讨论它们可能影响认知功能的机制。