Perineuronal Nets on CA2 Pyramidal Cells and Parvalbumin-Expressing Cells Differentially Regulate Hippocampal-Dependent Memory.

IF 4.4 2区 医学 Q1 NEUROSCIENCES
Georgia M Alexander, Viktoriya D Nikolova, Tristan M Stöber, Artiom Gruzdev, Sheryl S Moy, Serena M Dudek
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Abstract

Perineuronal nets (PNNs) are a specialized extracellular matrix that surrounds 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 knock-out mouse strains with the primary protein component of PNNs, aggrecan (Acan), deleted from either CA2 pyramidal cells (Amigo2 Acan KO) or from PV cells (PV Acan 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 Acan KO animals, but not PV Acan KO animals, had impaired social memory and reversal learning. PV Acan KOs, but not Amigo2 Acan 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 Acan KO animals and found reduced input to CA2 from the supramammillary nucleus (SuM), which signals social novelty. Additionally, Amigo2 Acan 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.

CA2锥体细胞和小蛋白表达细胞上的神经网络对海马依赖性记忆的调节存在差异。
神经周围网(PNNs)是一种特殊的细胞外基质,围绕着特定的神经元群,包括(抑制性)表达小白蛋白(PV)的中间神经元和(兴奋性)海马内的CA2锥体神经元。pnn被认为通过稳定突触来调节突触的可塑性,因此可以调节学习和记忆。大多数情况下,PNN功能是通过软骨素酶的酶降解来查询的,但这种方法并不能区分CA2神经元上的PNN与相邻PV细胞上的PNN。为了阐明PNNs在CA2锥体细胞和PV神经元行为中的具体作用,我们产生了条件敲除小鼠菌株,其中PNNs的主要蛋白质成分聚集蛋白(Acan)从CA2锥体细胞(Amigo2 Acan KO)或PV细胞(PV Acan KO)中删除。每个品系的雄性和雌性动物都接受了社交、恐惧、空间记忆以及逆向学习的测试。我们发现Amigo2 Acan KO动物,而不是PV Acan KO动物,有社会记忆和反转学习受损。PV - Acan KOs,而不是amig2 - Acan KOs的情境恐惧记忆受损。这些发现证明了PNNs在调节海马依赖性记忆中的独立作用。我们进一步研究了Amigo2 Acan KO动物社会记忆受损的潜在机制,发现乳上核(SuM)对CA2的输入减少,这是社会新颖性的信号。此外,Amigo2 Acan KOs缺乏与社会新颖性相关的局部场电位反应,这表明CA2 PNNs可能协调功能性SuM连接和相关的社会新颖性生理反应。周围神经元网(PNNs)围绕着抑制性小白蛋白(PV)表达神经元和兴奋性CA2锥体神经元,但先前使用酶降解的研究无法区分PNNs在两种人群中的相对作用。通过有条件地从CA2锥体神经元中删除聚合蛋白(Acan),而不影响PV细胞上的pnn,反之亦然,我们发现pnn在每种细胞类型的行为中起着不同的作用。需要CA2活动的社会记忆在缺乏CA2 PNNs的小鼠中受损,但在缺乏PV PNNs的小鼠中没有受损。在缺乏CA2 pnn的小鼠中,通过反向学习评估的认知灵活性也受到损害,而在缺乏PV pnn的小鼠中,情境恐惧记忆受到损害。因此,每种细胞类型上的PNNs对海马依赖记忆的不同形式有不同的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Neuroscience
Journal of Neuroscience 医学-神经科学
CiteScore
9.30
自引率
3.80%
发文量
1164
审稿时长
12 months
期刊介绍: JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles
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