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三方突触形成过程中神经元与神经胶质细胞之间的神经营养因子信号传导。

Neurotrophin signaling among neurons and glia during formation of tripartite synapses.

作者信息

Elmariah Sarina B, Hughes Ethan G, Oh Eun Joo, Balice-Gordon Rita J

机构信息

Department of Neuroscience, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6074, USA.

出版信息

Neuron Glia Biol. 2004 Nov;1(4):1-11. doi: 10.1017/S1740925X05000189.

Abstract

Synapse formation in the CNS is a complex process that involves the dynamic interplay of numerous signals exchanged between pre- and postsynaptic neurons as well as perisynaptic glia. Members of the neurotrophin family, which are widely expressed in the developing and mature CNS and are well-known for their roles in promoting neuronal survival and differentiation, have emerged as key synaptic modulators. However, the mechanisms by which neurotrophins modulate synapse formation and function are poorly understood. Here, we summarize our work on the role of neurotrophins in synaptogenesis in the CNS, in particular the role of these signaling molecules and their receptors, the Trks, in the development of excitatory and inhibitory hippocampal synapses. We discuss our results that demonstrate that postsynaptic TrkB signaling plays an important role in modulating the formation and maintenance of NMDA and GABAA receptor clusters at central synapses, and suggest that neurotrophin signaling coordinately modulates these receptors as part of mechanism that promotes the balance between excitation and inhibition in developing circuits. We also discuss our results that demonstrate that astrocytes promote the formation of GABAergic synapses in vitro by differentially regulating the development of inhibitory presynaptic terminals and postsynaptic GABAA receptor clusters, and suggest that glial modulation of inhibitory synaptogenesis is mediated by neurotrophin-dependent and -independent signaling. Together, these findings extend our understanding of how neuron-glia communication modulates synapse formation, maintenance and function, and set the stage for defining the cellular and molecular mechanisms by which neurotrophins and other cell-cell signals direct synaptogenesis in the developing brain.

摘要

中枢神经系统(CNS)中的突触形成是一个复杂的过程,涉及突触前和突触后神经元以及突触周围神经胶质细胞之间交换的众多信号的动态相互作用。神经营养因子家族的成员在发育中和成熟的中枢神经系统中广泛表达,并因其在促进神经元存活和分化中的作用而闻名,现已成为关键的突触调节剂。然而,神经营养因子调节突触形成和功能的机制尚不清楚。在这里,我们总结了我们关于神经营养因子在中枢神经系统突触发生中的作用的研究工作,特别是这些信号分子及其受体Trks在兴奋性和抑制性海马突触发育中的作用。我们讨论了我们的结果,这些结果表明突触后TrkB信号在调节中枢突触处NMDA和GABAA受体簇的形成和维持中起重要作用,并表明神经营养因子信号作为促进发育中回路兴奋与抑制平衡机制的一部分,协调调节这些受体。我们还讨论了我们的结果,这些结果表明星形胶质细胞通过差异调节抑制性突触前终末和突触后GABAA受体簇的发育来促进体外GABA能突触的形成,并表明神经胶质细胞对抑制性突触发生的调节是由神经营养因子依赖性和非依赖性信号介导的。这些发现共同扩展了我们对神经元 - 神经胶质细胞通讯如何调节突触形成、维持和功能的理解,并为确定神经营养因子和其他细胞间信号在发育中的大脑中指导突触发生的细胞和分子机制奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17a/1397704/001c39778749/nihms8720f1.jpg

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