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胚胎小鼠脑干中自发传播波的调控

Regulation of Spontaneous Propagating Waves in the Embryonic Mouse Brainstem.

作者信息

Bosma Martha M

机构信息

Department of Biology, University of Washington Seattle, WA, USA.

出版信息

Front Neural Circuits. 2017 Jan 4;10:110. doi: 10.3389/fncir.2016.00110. eCollection 2016.

DOI:10.3389/fncir.2016.00110
PMID:28101007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5209361/
Abstract

Spontaneous activity (SA) modulates many aspects of neural development, including neuronal phenotype, axon path-finding and synaptic connectivity. In the embryonic mouse brainstem, SA initially is recorded in isolated cells at embryonic day (E) 9.5, and 48 h later takes the form of propagating waves. The majority of these waves originate from one midline initiation zone (InZ), which is situated within the developing serotonergic raphe. InZ cells express a -type calcium channel, are depolarized, and have high membrane resistance, the combination of which allows spontaneous depolarization. Propagating events require signaling at metabotropic 5-HT receptors; a possible source could be 5-HT released by newly differentiating 5-HT neurons. At E11.5, waves propagate throughout the hindbrain, with some events crossing into the midbrain. At E12.5, lateral cells (further than 150 μm from the midline) up-regulate expression of a K channel that increases resting conductance and hyperpolarizes them, preventing the propagation of waves laterally. At the same stage, cells in the isthmus up-regulate -type calcium channels, permitting more events to cross into the midbrain, some of which form recurring loops of activity that are able to keep intracellular calcium levels high for many minutes. At E13.5, caudal hindbrain cells hyperpolarize utilizing the same K conductance, and 24 h later, at E14.5, the InZ hyperpolarizes and no longer undergoes spontaneous events. Thus, 5-HT receptor-dependent propagating waves in the embryonic brainstem are generated and propagated by regulation of membrane conductance. We discuss these mechanisms, and the possible role of this SA in neuronal development.

摘要

自发活动(SA)调节神经发育的许多方面,包括神经元表型、轴突路径寻找和突触连接。在胚胎小鼠脑干中,SA最初在胚胎第9.5天(E9.5)时在分离的细胞中被记录到,48小时后则以传播波的形式出现。这些波中的大多数起源于一个位于发育中的5-羟色胺能中缝核内的中线起始区(InZ)。InZ细胞表达α型钙通道,处于去极化状态,且具有高膜电阻,这些因素共同作用使得细胞能够自发去极化。传播事件需要代谢型5-羟色胺(5-HT)受体发出信号;一个可能的来源可能是新分化的5-HT神经元释放的5-HT。在E11.5时,波在整个后脑传播,一些事件会传入中脑。在E12.5时,外侧细胞(距离中线超过150μm)上调一种钾通道的表达,该通道增加静息电导并使其超极化,从而阻止波向外侧传播。在同一阶段,峡部的细胞上调α型钙通道,使得更多事件能够传入中脑,其中一些形成反复出现的活动环路,能够使细胞内钙水平在数分钟内保持较高。在E13.5时,尾侧后脑细胞利用相同的钾电导实现超极化,24小时后,即E14.5时,InZ超极化且不再发生自发事件。因此,胚胎脑干中依赖5-HT受体的传播波是通过膜电导的调节产生和传播的。我们讨论了这些机制,以及这种SA在神经元发育中可能发挥的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de26/5209361/302b41a491be/fncir-10-00110-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de26/5209361/ec8bfd6cc387/fncir-10-00110-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de26/5209361/302b41a491be/fncir-10-00110-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de26/5209361/ec8bfd6cc387/fncir-10-00110-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de26/5209361/302b41a491be/fncir-10-00110-g0002.jpg

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