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海马体特异性白细胞介素-15受体α缺陷导致小鼠出现更严重的焦虑样行为。

Hippocampus-specific deficiency of IL-15Rα contributes to greater anxiety-like behaviors in mice.

作者信息

Nguyen Linda, Bohlen Joseph, Stricker Janelle, Chahal Ikttesh, Zhang Hanting, Pistilli Emidio E

机构信息

Departments of Behavioral Medicine & Psychiatry and Physiology & Pharmacology, West Virginia University School of Medicine, Morgantown, WV, 26506, USA.

Division of Exercise Physiology, West Virginia University School of Medicine, Morgantown, WV, 26506, USA.

出版信息

Metab Brain Dis. 2017 Apr;32(2):297-302. doi: 10.1007/s11011-016-9930-y. Epub 2016 Nov 11.

DOI:10.1007/s11011-016-9930-y
PMID:27837366
Abstract

A hippocampus-specific IL15RαKO mouse (hipIl15ra /Cre) was generated to test the hypothesis that the targeted deletion of interleukin-15 receptor alpha (IL-15Rα) in the hippocampus contributes to altered behavior, including greater levels of anxiety and ambulatory activity. Using Cre-loxP, exons 2 and 3 of the IL-15Rα gene were excised within the hippocampus, while normal expression was maintained within the rest of the brain. In the open field test (OFT), hipIl15ra /Cre spent a greater amount of time in the periphery and less time in the central portions of the chamber, and there was also a noticeable trend for decreased rearing activity; these behaviors are consistent with greater levels of anxiety-like behavior in these mice. However, there were no differences in the overall locomotor counts in the OFT when comparing hipIl15ra /Cre mice to their littermate controls. These data implicate IL-15-related signaling within the hippocampus has a role in anxiety-like behavior.

摘要

为了验证海马体中白细胞介素-15受体α(IL-15Rα)的靶向缺失会导致行为改变(包括更高水平的焦虑和活动能力)这一假设,我们构建了一种海马体特异性IL15Rα基因敲除小鼠(hipIl15ra /Cre)。利用Cre-loxP系统,在海马体内切除了IL-15Rα基因的第2和第3外显子,而在大脑的其他部分维持正常表达。在旷场试验(OFT)中,hipIl15ra /Cre小鼠在试验箱外周花费的时间更多,在中央部分花费的时间更少,并且竖毛活动减少的趋势也很明显;这些行为与这些小鼠更高水平的焦虑样行为一致。然而,将hipIl15ra /Cre小鼠与其同窝对照小鼠相比,旷场试验中的总体运动计数没有差异。这些数据表明,海马体内与IL-15相关的信号传导在焦虑样行为中起作用。

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Biochem Biophys Res Commun. 2015 Mar 13;458(3):614-619. doi: 10.1016/j.bbrc.2015.02.015. Epub 2015 Feb 11.
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Front Physiol. 2019 Nov 26;10:1439. doi: 10.3389/fphys.2019.01439. eCollection 2019.
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