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通过对桶状皮层 VIP 神经元进行全脑输入映射揭示 Reeler 小鼠胼胝体连接增加。

Increased Callosal Connectivity in Reeler Mice Revealed by Brain-Wide Input Mapping of VIP Neurons in Barrel Cortex.

机构信息

Institute for Neuroanatomy, University Medical Center, Georg-August-University Göttingen, 37075 Göttingen, Germany.

Functional Imaging Laboratory, German Primate Center, Leibniz Institute for Primate Research, 37077 Göttingen, Germany.

出版信息

Cereb Cortex. 2021 Feb 5;31(3):1427-1443. doi: 10.1093/cercor/bhaa280.

DOI:10.1093/cercor/bhaa280
PMID:33135045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7869096/
Abstract

The neocortex is composed of layers. Whether layers constitute an essential framework for the formation of functional circuits is not well understood. We investigated the brain-wide input connectivity of vasoactive intestinal polypeptide (VIP) expressing neurons in the reeler mouse. This mutant is characterized by a migration deficit of cortical neurons so that no layers are formed. Still, neurons retain their properties and reeler mice show little cognitive impairment. We focused on VIP neurons because they are known to receive strong long-range inputs and have a typical laminar bias toward upper layers. In reeler, these neurons are more dispersed across the cortex. We mapped the brain-wide inputs of VIP neurons in barrel cortex of wild-type and reeler mice with rabies virus tracing. Innervation by subcortical inputs was not altered in reeler, in contrast to the cortical circuitry. Numbers of long-range ipsilateral cortical inputs were reduced in reeler, while contralateral inputs were strongly increased. Reeler mice had more callosal projection neurons. Hence, the corpus callosum was larger in reeler as shown by structural imaging. We argue that, in the absence of cortical layers, circuits with subcortical structures are maintained but cortical neurons establish a different network that largely preserves cognitive functions.

摘要

新皮层由层组成。层是否构成功能回路形成的基本框架尚不清楚。我们研究了 reeler 小鼠中血管活性肠肽 (VIP) 表达神经元的全脑输入连接。这种突变的特征是皮质神经元迁移不足,因此没有形成层。尽管如此,神经元仍保留其特性,reeler 小鼠的认知障碍很小。我们专注于 VIP 神经元,因为它们已知接收强烈的长程输入,并且具有向上层的典型层偏置。在 reeler 中,这些神经元在皮层中更加分散。我们使用狂犬病病毒追踪法在野生型和 reeler 小鼠的桶状皮层中绘制了 VIP 神经元的全脑输入图。与皮质回路相反,reeler 中的皮质下输入的神经支配没有改变。长程同侧皮质输入的数量在 reeler 中减少,而对侧输入则大大增加。reeler 小鼠有更多的胼胝体投射神经元。因此,结构成像显示 reeler 中的胼胝体较大。我们认为,在没有皮质层的情况下,维持了与皮质下结构的回路,但皮质神经元建立了一个不同的网络,在很大程度上保留了认知功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/ce282327650e/bhaa280f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/41f47fe73635/bhaa280f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/6b6741b49d52/bhaa280f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/b01c2b587c46/bhaa280f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/5186dbea7dde/bhaa280f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/0f453b2e10d9/bhaa280f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/ce282327650e/bhaa280f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/41f47fe73635/bhaa280f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/5f909aa80b07/bhaa280f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/6b6741b49d52/bhaa280f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/b01c2b587c46/bhaa280f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/5186dbea7dde/bhaa280f5.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c73/7869096/ce282327650e/bhaa280f7.jpg

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