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少突胶质细胞通过脑脑干中的 BDNF 信号调节突触前特性和神经传递。

Oligodendrocytes regulate presynaptic properties and neurotransmission through BDNF signaling in the mouse brainstem.

机构信息

The Department of Cellular and Integrative Physiology, University of Texas Health Science Center, San Antonio, United States.

Children's Medical Center, The Second Xiangya Hospital, Central South University, Changsha, China.

出版信息

Elife. 2019 Apr 18;8:e42156. doi: 10.7554/eLife.42156.

Abstract

Neuron-glia communication contributes to the fine-tuning of synaptic functions. Oligodendrocytes near synapses detect and respond to neuronal activity, but their role in synapse development and plasticity remains largely unexplored. We show that oligodendrocytes modulate neurotransmitter release at presynaptic terminals through secretion of brain-derived neurotrophic factor (BDNF). Oligodendrocyte-derived BDNF functions via presynaptic tropomyosin receptor kinase B (TrkB) to ensure fast, reliable neurotransmitter release and auditory transmission in the developing brain. In auditory brainstem slices from mice, reduction in endogenous BDNF significantly decreased vesicular glutamate release by reducing the readily releasable pool of glutamate vesicles, without altering presynaptic Ca channel activation or release probability. Using conditional knockout mice, cell-specific ablation of BDNF in oligodendrocytes largely recapitulated this effect, which was recovered by BDNF or TrkB agonist application. This study highlights a novel function for oligodendrocytes in synaptic transmission and their potential role in the activity-dependent refinement of presynaptic properties.

摘要

神经元-胶质细胞通讯有助于突触功能的微调。突触附近的少突胶质细胞检测和响应神经元活动,但它们在突触发育和可塑性中的作用在很大程度上仍未得到探索。我们表明,少突胶质细胞通过分泌脑源性神经营养因子 (BDNF) 来调节突触前末梢的神经递质释放。少突胶质细胞衍生的 BDNF 通过突触前原肌球蛋白受体激酶 B (TrkB) 发挥作用,以确保发育中的大脑中快速、可靠的神经递质释放和听觉传递。在 小鼠的听觉脑干切片中,内源性 BDNF 的减少通过减少谷氨酸囊泡的易释放池显著降低了囊泡谷氨酸的释放,而不改变突触前 Ca 通道的激活或释放概率。使用条件性敲除小鼠,在少突胶质细胞中特异性消融 BDNF 很大程度上再现了这种效应,而 BDNF 或 TrkB 激动剂的应用则恢复了这种效应。这项研究强调了少突胶质细胞在突触传递中的新功能及其在活动依赖性增强突触特性中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dfe/6504230/9c86305b8d5d/elife-42156-fig1.jpg

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