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使用全面的行为测试组合对 Caskin1 蛋白的分布及其敲除小鼠的表型特征进行研究。

Distribution of Caskin1 protein and phenotypic characterization of its knockout mice using a comprehensive behavioral test battery.

机构信息

Department of Medical Chemistry, Kansai Medical University, Hirakata, 573-1010, Japan.

Section of Behavior Patterns, National Institute of Physiological Sciences NINS, Okazaki, Aichi, 444-8585, Japan.

出版信息

Mol Brain. 2018 Oct 25;11(1):63. doi: 10.1186/s13041-018-0407-2.

Abstract

Calcium/calmodulin-dependent serine protein kinase (CASK)-interacting protein 1 (Caskin1) is a direct binding partner of the synaptic adaptor protein CASK. Because Caskin1 forms homo-multimers and binds not only CASK but also other neuronal proteins in vitro, it is anticipated to have neural functions; but its exact role in mammals remains unclear. Previously, we showed that the concentration of Caskin1 in the spinal dorsal horn increases under chronic pain. To characterize this protein, we generated Caskin1-knockout (Caskin1-KO) mice and specific anti-Caskin1 antibodies. Biochemical and immunohistochemical analyses demonstrated that Caskin1 was broadly distributed in the whole brain and spinal cord, and that it primarily localized at synapses. To elucidate the neural function of Caskin1 in vivo, we subjected Caskin1-KO mice to comprehensive behavioral analysis. The mutant mice exhibited differences in gait, enhanced nociception, and anxiety-like behavior relative to their wild-type littermates. In addition, the knockouts exhibited strong freezing responses, with or without a cue tone, in contextual and cued-fear conditioning tests as well as low memory retention in the Barnes Maze test. Taken together, these results suggest that Caskin1 contributes to a wide spectrum of behavioral phenotypes, including gait, nociception, memory, and stress response, in broad regions of the central nervous system.

摘要

钙/钙调蛋白依赖性丝氨酸蛋白激酶(CASK)-相互作用蛋白 1(Caskin1)是突触衔接蛋白 CASK 的直接结合伴侣。由于 Caskin1 形成同源多聚体,不仅与 CASK 结合,而且在体外还与其他神经元蛋白结合,预计它具有神经功能;但它在哺乳动物中的确切作用尚不清楚。先前,我们表明 Caskin1 在慢性疼痛下在脊髓背角中的浓度增加。为了表征这种蛋白质,我们生成了 Caskin1 敲除(Caskin1-KO)小鼠和特异性抗 Caskin1 抗体。生化和免疫组织化学分析表明,Caskin1 在整个大脑和脊髓中广泛分布,主要定位于突触。为了阐明 Caskin1 在体内的神经功能,我们对 Caskin1-KO 小鼠进行了全面的行为分析。与野生型同窝仔相比,突变小鼠表现出步态差异、痛觉过敏增强和焦虑样行为。此外,敲除小鼠在情境和线索恐惧条件反射测试中表现出强烈的冻结反应,无论有无提示音,以及在 Barnes 迷宫测试中记忆保留能力低。总之,这些结果表明 Caskin1 有助于广泛的行为表型,包括步态、痛觉过敏、记忆和应激反应,在中枢神经系统的广泛区域。

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