Department of Cell Biology, Duke University Medical Center, 333A Nanaline Duke Bldg., Box 3709, Durham, NC 27710, United States.
Curr Opin Neurobiol. 2009 Oct;19(5):491-7. doi: 10.1016/j.conb.2009.09.007. Epub 2009 Oct 29.
Historically, our understanding of synapse formation has been shaped by studies focusing on neurons. However, with advancements in live imaging techniques and molecular and genetic tools we are rapidly uncovering new roles for glia in synapse formation and function. Contact-mediated signals from glia instruct dendrites to become receptive to synaptic partners. Glia-secreted factors coordinate the assembly and apposition of pre-synaptic and post-synaptic specializations. Glial cells also provide cues that are required for synaptic maturation and remodeling of spines both during development and in the adult. As we continue to learn about glial contributions to synapse formation and maintenance, it is likely that glia-derived signals will emerge as potential therapeutic targets for diseases that involve aberrant circuit function such as autism, epilepsy and Alzheimer's Disease.
从历史上看,我们对突触形成的理解受到了专注于神经元研究的影响。然而,随着活细胞成像技术以及分子和遗传工具的进步,我们正在迅速揭示出胶质细胞在突触形成和功能中的新作用。胶质细胞的接触介导信号指导树突变得能够接受突触伙伴。胶质细胞分泌的因子协调突触前和突触后特化的组装和贴合。胶质细胞还为突触成熟以及在发育和成年期的脊柱重塑提供线索。随着我们继续了解胶质细胞对突触形成和维持的贡献,很可能源自胶质细胞的信号将成为涉及异常电路功能的疾病(如自闭症、癫痫和阿尔茨海默病)的潜在治疗靶点。