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血管活性肠肽中间神经元在神经发育障碍中的作用。

A Role for Vasoactive Intestinal Peptide Interneurons in Neurodevelopmental Disorders.

机构信息

Medical Scientist Training Program (MSTP), The University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

Neuroscience Graduate Group, The University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

出版信息

Dev Neurosci. 2021;43(3-4):168-180. doi: 10.1159/000515264. Epub 2021 Apr 1.

DOI:10.1159/000515264
PMID:33794534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8440337/
Abstract

GABAergic inhibitory interneurons of the cerebral cortex expressing vasoactive intestinal peptide (VIP-INs) are rapidly emerging as important regulators of network dynamics and normal circuit development. Several recent studies have also identified VIP-IN dysfunction in models of genetically determined neurodevelopmental disorders (NDDs). In this article, we review the known circuit functions of VIP-INs and how they may relate to accumulating evidence implicating VIP-INs in the mechanisms of prominent NDDs. We highlight recurring VIP-IN-mediated circuit motifs that are shared across cerebral cortical areas and how VIP-IN activity can shape sensory input, development, and behavior. Ultimately, we extract a set of themes that inform our understanding of how VIP-INs influence pathogenesis of NDDs. Using publicly available single-cell RNA sequencing data from the Allen Institute, we also identify several underexplored disease-associated genes that are highly expressed in VIP-INs. We survey these genes and their shared related disease phenotypes that may broadly implicate VIP-INs in autism spectrum disorder and intellectual disability rather than epileptic encephalopathy. Finally, we conclude with a discussion of the relevance of cell type-specific investigations and therapeutics in the age of genomic diagnosis and targeted therapeutics.

摘要

大脑皮层表达血管活性肠肽的 GABA 能抑制性中间神经元(VIP-INs)正在迅速成为调节网络动态和正常回路发育的重要调节因子。最近的几项研究还在遗传决定的神经发育障碍(NDDs)模型中发现了 VIP-IN 功能障碍。在本文中,我们回顾了已知的 VIP-IN 回路功能,以及它们如何与越来越多的证据表明 VIP-INs 参与 NDD 机制相关联。我们强调了跨大脑皮质区域共享的 VIP-IN 介导的回路基序,以及 VIP-IN 活性如何影响感觉输入、发育和行为。最终,我们提取了一组主题,这些主题使我们能够了解 VIP-INs 如何影响 NDD 的发病机制。我们还使用艾伦研究所的公开可用的单细胞 RNA 测序数据,鉴定了几个在 VIP-INs 中高度表达的未充分研究的疾病相关基因。我们调查了这些基因及其共享的相关疾病表型,这些表型可能广泛暗示 VIP-INs 与自闭症谱系障碍和智力障碍有关,而不是癫痫性脑病。最后,我们讨论了在基因组诊断和靶向治疗时代,细胞类型特异性研究和治疗的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/8440337/3e723dcc1601/nihms-1676689-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/8440337/21c457824b27/nihms-1676689-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/8440337/ca2acdca67c8/nihms-1676689-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/8440337/3e723dcc1601/nihms-1676689-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/8440337/21c457824b27/nihms-1676689-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/8440337/ca2acdca67c8/nihms-1676689-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e97/8440337/3e723dcc1601/nihms-1676689-f0003.jpg

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