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前外侧桶状亚区在形态和细胞密度上与后内侧桶状亚区的 parvalbumin 阳性 GABA 能中间神经元不同。

The Anterolateral Barrel Subfield Differs from the Posteromedial Barrel Subfield in the Morphology and Cell Density of Parvalbumin-Positive GABAergic Interneurons.

机构信息

Department of Anatomy and Neurobiology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan.

Department of Anatomy and Neurobiology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan

出版信息

eNeuro. 2024 Mar 26;11(3). doi: 10.1523/ENEURO.0518-22.2024. Print 2024 Mar.

DOI:10.1523/ENEURO.0518-22.2024
PMID:38438262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10965236/
Abstract

Layer 4 of the rodent somatosensory cortex has unitary structures called barrels that receive tactile information from individual vibrissae. Barrels in the anterolateral barrel subfield (ALBSF) are much smaller and have gained less attention than larger barrels in the posteromedial barrel subfield (PMBSF), though the former outnumber the latter. We compared the morphological features of barrels between the ALBSF and PMBSF in male mice using deformation-free tangential sections and confocal optical slice-based, precise reconstructions of barrels. The average volume of a single barrel in the ALBSF was 34.7% of that in the PMBSF, but the numerical density of parvalbumin (PV)-positive interneurons in the former was 1.49 times higher than that in the latter. Moreover, PV neuron density in septa was 2.08 times higher in the ALBSF than that in the PMBSF. The proportions of PV neuron number to both all neuron number and all GABAergic neuron number in the ALBSF were also higher than those in the PMBSF. Somata of PV neurons in barrels and septa in the ALBSF received 1.64 and 1.50 times more vesicular glutamate transporter Type 2-labeled boutons than those in the PMBSF, suggesting more potent feedforward inhibitory circuits in the ALBSF. The mode of connectivity through dendritic gap junctions among PV neurons also differed between the ALBSF and PMBSF. Clusters of smaller unitary structures containing a higher density of representative GABAergic interneurons with differential morphological features in the ALBSF suggest a division of functional roles in the two vibrissa-barrel systems, as has been demonstrated by behavioral studies.

摘要

鼠体感皮层第 4 层具有称为桶状结构的单一结构,这些结构接收来自单个触须的触觉信息。在前外侧桶状亚区 (ALBSF) 的桶状结构比后内侧桶状亚区 (PMBSF) 的桶状结构小得多,也受到的关注少得多,尽管前者的数量比后者多。我们使用无变形切向切片和基于共聚焦光片的、对桶状结构进行精确重建的方法,比较了雄性小鼠 ALBSF 和 PMBSF 之间桶状结构的形态特征。ALBSF 中单个桶状结构的平均体积为 PMBSF 的 34.7%,但前者的 parvalbumin (PV) 阳性中间神经元的数量密度比后者高 1.49 倍。此外,ALBSF 中的隔区 PV 神经元密度比 PMBSF 高 2.08 倍。ALBSF 中 PV 神经元数与所有神经元数和所有 GABA 能神经元数的比例也高于 PMBSF。ALBSF 中桶状结构和隔区的 PV 神经元胞体接受的囊泡谷氨酸转运体 2 标记的末梢比 PMBSF 中的多 1.64 倍和 1.50 倍,提示 ALBSF 中存在更强的前馈抑制回路。PV 神经元通过树突间隙连接的连接模式在 ALBSF 和 PMBSF 之间也存在差异。ALBSF 中含有更高密度具有不同形态特征的代表性 GABA 能中间神经元的较小单元结构簇表明,两个触须-桶状系统的功能作用存在分工,这已被行为研究证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/bdcd1188b937/eneuro-11-ENEURO.0518-22.2024-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/d1bd0c0f080a/eneuro-11-ENEURO.0518-22.2024-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/67ce9089d807/eneuro-11-ENEURO.0518-22.2024-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/29b29bfaa30a/eneuro-11-ENEURO.0518-22.2024-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/b33c7a8d36a9/eneuro-11-ENEURO.0518-22.2024-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/73ca90d2b79d/eneuro-11-ENEURO.0518-22.2024-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/b0be913c2bac/eneuro-11-ENEURO.0518-22.2024-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/d4d0c6a623a1/eneuro-11-ENEURO.0518-22.2024-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/b3b1834b7b95/eneuro-11-ENEURO.0518-22.2024-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/bdcd1188b937/eneuro-11-ENEURO.0518-22.2024-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/d1bd0c0f080a/eneuro-11-ENEURO.0518-22.2024-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/67ce9089d807/eneuro-11-ENEURO.0518-22.2024-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/29b29bfaa30a/eneuro-11-ENEURO.0518-22.2024-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/b33c7a8d36a9/eneuro-11-ENEURO.0518-22.2024-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/73ca90d2b79d/eneuro-11-ENEURO.0518-22.2024-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/b0be913c2bac/eneuro-11-ENEURO.0518-22.2024-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/d4d0c6a623a1/eneuro-11-ENEURO.0518-22.2024-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/b3b1834b7b95/eneuro-11-ENEURO.0518-22.2024-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6665/10965236/bdcd1188b937/eneuro-11-ENEURO.0518-22.2024-g009.jpg

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