Kiraly Drew D, Eipper-Mains Jodi E, Mains Richard E, Eipper Betty A
Department of Neuroscience, University of Connecticut Health Center, Farmington, CT.
ACS Chem Neurosci. 2010 May 19;1(5):348-365. doi: 10.1021/cn100012x.
Dendritic spines are the postsynaptic sites for the majority of excitatory synapses in the mammalian forebrain. While many spines display great stability, others change shape in a matter of seconds to minutes. These rapid alterations in dendritic spine number and size require tight control of the actin cytoskeleton, the main structural component of dendritic spines. The ability of neurons to alter spine number and size is essential for the expression of neuronal plasticity. Within spines, guanine nucleotide exchange factors (GEFs) act as critical regulators of the actin cytoskeleton by controlling the activity of Rho-GTPases. In this review we focus on the Rho-GEFs expressed in the nucleus accumbens and localized to the postsynaptic density, and thus positioned to effect rapid alterations in the structure of dendritic spines. We review literature that ties these GEFs to different receptor systems and intracellular signaling cascades and discuss the effects these interactions are likely to have on synaptic plasticity.
树突棘是哺乳动物前脑大多数兴奋性突触的突触后位点。虽然许多树突棘表现出很强的稳定性,但其他树突棘会在几秒到几分钟内改变形状。树突棘数量和大小的这些快速变化需要对肌动蛋白细胞骨架进行严格控制,肌动蛋白细胞骨架是树突棘的主要结构成分。神经元改变树突棘数量和大小的能力对于神经元可塑性的表达至关重要。在树突棘内,鸟嘌呤核苷酸交换因子(GEFs)通过控制Rho-GTPases的活性,作为肌动蛋白细胞骨架的关键调节因子。在本综述中,我们重点关注伏隔核中表达并定位于突触后致密区的Rho-GEFs,因此它们能够影响树突棘结构的快速变化。我们回顾了将这些GEFs与不同受体系统和细胞内信号级联联系起来的文献,并讨论了这些相互作用可能对突触可塑性产生的影响。