Muly E Chris, Nairn Angus C, Greengard Paul, Rainnie Donald G
Department of Psychiatry and Behavioral Sciences, Yerkes National Primate Research Center, Atlanta, Georgia 30322, USA.
J Comp Neurol. 2008 Jun 20;508(6):927-39. doi: 10.1002/cne.21703.
The strength of synaptic connections in the brain varies with activity, and this plasticity depends on remodeling of the actin cytoskeleton in dendritic spines. Critical to this are the Rho family GTPases, whose activity is controlled by various modulatory proteins, including the Rho-GEF Lfc. In cultured neurons and nonneuronal cells, Lfc has been shown both to bind to microtubules and to regulate the actin cytoskeleton. Significantly, Lfc was found to be concentrated in the dendritic shafts of cultured hippocampal neurons under control conditions but then translocated into spines when neural activity was stimulated. In this study, we used immunohistochemistry and electron microscopy to examine activity-dependent changes in the distribution of Lfc in the neuropil of monkey prefrontal cortex. We found that, although Lfc was concentrated in dendrites, it also had a complex distribution in the neuropil, including being present in spines, axons, terminals, and glial processes. Moreover, Lfc distribution varied in different layers of cortex. By using an in vitro slice preparation of monkey prefrontal cortex, we demonstrated an activity-dependent translocation of Lfc from dendritic shafts to spines. The results of this study support a role for Lfc in activity-dependent spine plasticity and demonstrate the feasibility of studying activity-dependent changes in protein localization in tissue slices.
大脑中突触连接的强度随活动而变化,这种可塑性取决于树突棘中肌动蛋白细胞骨架的重塑。对此至关重要的是Rho家族小G蛋白,其活性受多种调节蛋白控制,包括Rho鸟苷酸交换因子Lfc。在培养的神经元和非神经元细胞中,Lfc已被证明既能与微管结合,又能调节肌动蛋白细胞骨架。值得注意的是,在对照条件下,Lfc集中在培养的海马神经元的树突干中,但在刺激神经活动时会转移到树突棘中。在本研究中,我们使用免疫组织化学和电子显微镜来检查猴前额叶皮质神经毡中Lfc分布的活动依赖性变化。我们发现,虽然Lfc集中在树突中,但它在神经毡中也有复杂的分布,包括存在于树突棘、轴突、终末和胶质细胞突起中。此外,Lfc分布在皮质的不同层中有所不同。通过使用猴前额叶皮质的体外脑片制备,我们证明了Lfc从树突干到树突棘的活动依赖性转移。本研究结果支持Lfc在活动依赖性树突棘可塑性中的作用,并证明了研究组织切片中蛋白质定位的活动依赖性变化的可行性。