Gerges Nashaat Z, Brown Tyler C, Correia Susana S, Esteban José A
Methods Enzymol. 2005;403:153-66. doi: 10.1016/S0076-6879(05)03013-2.
Members of the Rab family of small GTPases are essential regulators of intracellular membrane sorting. Nevertheless, very little is known about the role of these proteins in the membrane trafficking processes that operate at synapses, and specifically, at postsynaptic terminals. These events include the activity-dependent exocytic and endocytic trafficking of AMPA-type glutamate receptors, which underlies long-lasting forms of synaptic plasticity such as long-term potentiation (LTP) and long-term depression (LTD). This chapter summarizes different experimental methods to address the role of Rab proteins in the trafficking of neurotransmitter receptors at postsynaptic terminals in the hippocampus. These techniques include immunogold electron microscopy to ultrastructurally localize endogenous Rab proteins at synapses, molecular biology methods to express recombinant Rab proteins in hippocampal slice cultures, electrophysiological techniques to evaluate the role of Rab proteins in synaptic transmission, and confocal fluorescence imaging to monitor receptor trafficking at dendrites and spines and its dependence on Rab proteins.
小GTP酶Rab家族的成员是细胞内膜分选的重要调节因子。然而,对于这些蛋白质在突触尤其是突触后终端进行的膜运输过程中的作用,我们知之甚少。这些过程包括AMPA型谷氨酸受体的活性依赖性胞吐和内吞运输,这是长期突触可塑性如长时程增强(LTP)和长时程抑制(LTD)的基础。本章总结了不同的实验方法,以研究Rab蛋白在海马体突触后终端神经递质受体运输中的作用。这些技术包括免疫金电子显微镜,用于在超微结构水平上定位突触中的内源性Rab蛋白;分子生物学方法,用于在海马脑片培养物中表达重组Rab蛋白;电生理技术,用于评估Rab蛋白在突触传递中的作用;以及共聚焦荧光成像,用于监测树突和棘突处的受体运输及其对Rab蛋白的依赖性。