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缺乏 Ig 细胞黏附分子 BT-IgSF(IgSF11)会导致在开放式迷宫、水迷宫和常驻入侵者测试中出现行为变化。

Lack of the Ig cell adhesion molecule BT-IgSF (IgSF11) induced behavioral changes in the open maze, water maze and resident intruder test.

机构信息

Neurogenetics Laboratory, Leibniz Institute for Neurobiology, Magdeburg, Germany.

Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.

出版信息

PLoS One. 2023 Jan 6;18(1):e0280133. doi: 10.1371/journal.pone.0280133. eCollection 2023.

Abstract

The brain- and testis-specific Ig superfamily protein (BT-IgSF, also termed IgSF11) is a homotypic cell adhesion protein. In the nervous system, BT-IgSF regulates the stability of AMPA receptors in the membrane of cultured hippocampal neurons, modulates the connectivity of chandelier cells and controls gap junction-mediated astrocyte-astrocyte communication. Here, we performed behavioral tests in BT-IgSF-deficient mice. BT-IgSF-deficient mice were similar to control littermates with respect to their reflexes, motor coordination and gating, and associative learning. However, BT-IgSF-deficient mice displayed an increased tendency to stay in the central illuminated areas in the open field and O-Maze paradigms suggesting reduced anxiety or increased scotophobia (fear of darkness). Although BT-IgSF-deficient mice initially found the platform in the water maze their behavior was compromised when the platform was moved, indicating reduced behavioral flexibility. This deficit was overcome by longer training to improve their spatial memory. Furthermore, male BT-IgSF-deficient mice displayed increased aggression towards an intruder. Our results show that specific behaviors are modified by the lack of BT-IgSF and demonstrate a contribution of BT-IgSF to network functions.

摘要

脑和睾丸特异性免疫球蛋白超家族蛋白(BT-IgSF,也称为 IgSF11)是一种同型细胞黏附蛋白。在神经系统中,BT-IgSF 调节培养海马神经元中 AMPA 受体在膜中的稳定性,调节 Chandelier 细胞的连接,并控制间隙连接介导的星形胶质细胞-星形胶质细胞通讯。在这里,我们在 BT-IgSF 缺陷小鼠中进行了行为测试。BT-IgSF 缺陷小鼠在反射、运动协调和门控以及联想学习方面与对照同窝仔相似。然而,BT-IgSF 缺陷小鼠在旷场和 O 迷宫范式中表现出留在中央光照区域的趋势增加,表明焦虑减少或对黑暗的恐惧(黑暗恐惧症)增加。尽管 BT-IgSF 缺陷小鼠最初在水迷宫中找到了平台,但当平台移动时,它们的行为受到了损害,表明行为灵活性降低。通过延长训练来提高空间记忆,克服了这一缺陷。此外,雄性 BT-IgSF 缺陷小鼠对入侵者表现出更强的攻击性。我们的结果表明,特定的行为受到 BT-IgSF 缺乏的影响,并证明了 BT-IgSF 对网络功能的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3b0/9821459/7c0e6e705914/pone.0280133.g001.jpg

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