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CA2锥体细胞和表达小白蛋白的细胞上的神经周网对海马体依赖性记忆有不同的调节作用。

Perineuronal nets on CA2 pyramidal cells and parvalbumin-expressing cells differentially regulate hippocampal dependent memory.

作者信息

Alexander Georgia M, Nikolova Viktoriya D, Stöber Tristan M, Gruzdev Artiom, Moy Sheryl S, Dudek Serena M

机构信息

Neurobiology Laboratory, National Institute of Environmental Health Sciences, Division of Intramural Research, National Institute of Health, Research Triangle Park, North Carolina 27713, USA.

Carolina Institute for Developmental Disabilities and Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599, USA.

出版信息

bioRxiv. 2024 Nov 8:2024.11.07.622463. doi: 10.1101/2024.11.07.622463.

DOI:10.1101/2024.11.07.622463
PMID:39574580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11581025/
Abstract

Perineuronal nets (PNNs) are a specialized extracellular matrix that surround certain populations of neurons, including (inhibitory) parvalbumin (PV) expressing-interneurons throughout the brain and (excitatory) CA2 pyramidal neurons in hippocampus. PNNs are thought to regulate synaptic plasticity by stabilizing synapses and as such, could regulate learning and memory. Most often, PNN functions are queried using enzymatic degradation with chondroitinase, but that approach does not differentiate PNNs on CA2 neurons from those on adjacent PV cells. To disentangle the specific roles of PNNs on CA2 pyramidal cells and PV neurons in behavior, we generated conditional knockout mouse strains with the primary protein component of PNNs, aggrecan (), deleted from either CA2 pyramidal cells (Amigo2 KO) or from PV cells (PV KO). Male and female animals of each strain were tested for social, fear, and spatial memory, as well as for reversal learning. We found that Amigo2 KO animals, but not PV KO animals, had impaired social memory and reversal learning. PV KOs, but not Amigo2 KOs had impaired contextual fear memory. These findings demonstrate independent roles for PNNs on each cell type in regulating hippocampal-dependent memory. We further investigated a potential mechanism of impaired social memory in the Amigo2 KO animals and found reduced input to CA2 from the supramammillary nucleus (SuM), which signals social novelty. Additionally, Amigo2 KOs lacked a social novelty-related local field potential response, suggesting that CA2 PNNs may coordinate functional SuM connections and associated physiological responses to social novelty.

摘要

神经元周围网络(PNNs)是一种特殊的细胞外基质,围绕着特定的神经元群体,包括大脑中表达(抑制性)小白蛋白(PV)的中间神经元以及海马体中的(兴奋性)CA2锥体神经元。人们认为PNNs通过稳定突触来调节突触可塑性,因此可能调节学习和记忆。最常见的是,使用软骨素酶进行酶促降解来探究PNN的功能,但这种方法无法区分CA2神经元上的PNNs与相邻PV细胞上的PNNs。为了弄清楚PNNs在行为中对CA2锥体细胞和PV神经元的特定作用,我们构建了条件性基因敲除小鼠品系,从CA2锥体细胞(Amigo2基因敲除)或PV细胞(PV基因敲除)中删除了PNNs的主要蛋白质成分聚集蛋白聚糖。对每个品系的雄性和雌性动物进行社交、恐惧和空间记忆以及逆向学习测试。我们发现,Amigo2基因敲除动物而非PV基因敲除动物的社交记忆和逆向学习受损。PV基因敲除动物而非Amigo2基因敲除动物的情境恐惧记忆受损。这些发现表明PNNs在调节海马体依赖性记忆方面对每种细胞类型具有独立作用。我们进一步研究了Amigo2基因敲除动物社交记忆受损的潜在机制,发现来自乳头体上核(SuM)向CA2的输入减少,SuM传递社交新奇性信号。此外,Amigo2基因敲除动物缺乏与社交新奇性相关的局部场电位反应,这表明CA2的PNNs可能协调功能性SuM连接以及对社交新奇性的相关生理反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/179b23b347c1/nihpp-2024.11.07.622463v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/09078c52c47d/nihpp-2024.11.07.622463v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/94de7b23514f/nihpp-2024.11.07.622463v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/e92befdad175/nihpp-2024.11.07.622463v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/a2a922a08e5c/nihpp-2024.11.07.622463v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/c28ad269e251/nihpp-2024.11.07.622463v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/6956bec00857/nihpp-2024.11.07.622463v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/23f814202a2e/nihpp-2024.11.07.622463v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/179b23b347c1/nihpp-2024.11.07.622463v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/09078c52c47d/nihpp-2024.11.07.622463v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/94de7b23514f/nihpp-2024.11.07.622463v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/e92befdad175/nihpp-2024.11.07.622463v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/a2a922a08e5c/nihpp-2024.11.07.622463v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/c28ad269e251/nihpp-2024.11.07.622463v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/6956bec00857/nihpp-2024.11.07.622463v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/23f814202a2e/nihpp-2024.11.07.622463v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf5a/11581025/179b23b347c1/nihpp-2024.11.07.622463v1-f0006.jpg

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Silencing hippocampal CA2 reduces behavioral flexibility in spatial learning.沉默海马 CA2 减少空间学习中的行为灵活性。
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Elimination of perineuronal nets in CA1 disrupts GABA release and long-term contextual fear memory retention.
CA1 区周围神经毡的消除会破坏 GABA 的释放和长期的情境性恐惧记忆保留。
Hippocampus. 2023 Jul;33(7):862-871. doi: 10.1002/hipo.23503. Epub 2023 Jan 28.
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Postnatal development of hippocampal CA2 structure and function during the emergence of social recognition of peers.在同伴社会识别出现期间,海马 CA2 结构和功能的产后发育。
Hippocampus. 2023 Mar;33(3):208-222. doi: 10.1002/hipo.23476. Epub 2022 Oct 30.
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Altered inhibitory function in hippocampal CA2 contributes in social memory deficits in Alzheimer's mouse model.海马体CA2区抑制功能改变导致阿尔茨海默病小鼠模型出现社交记忆缺陷。
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