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小鼠体内的α-抑制因子间缺乏与焦虑样行为、探索行为和社交趋近行为的改变有关。

Inter-α-inhibitor deficiency in the mouse is associated with alterations in anxiety-like behavior, exploration and social approach.

作者信息

Goulding David R, Nikolova Viktoriya D, Mishra Lopa, Zhuo Lisheng, Kimata Koji, McBride Sandra J, Moy Sheryl S, Harry G J, Garantziotis Stavros

机构信息

Comparative Medicine Branch, Division of Intramural Research, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.

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

出版信息

Genes Brain Behav. 2019 Jan;18(1):e12505. doi: 10.1111/gbb.12505. Epub 2018 Aug 6.

DOI:10.1111/gbb.12505
PMID:29987918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6328341/
Abstract

In recent years, several genome-wide association studies have identified candidate regions for genetic susceptibility in major mood disorders. Most notable are regions in a locus in chromosome 3p21, encompassing the genes NEK4-ITIH1-ITIH3-ITIH4. Three of these genes represent heavy chains of the composite protein inter-α-inhibitor (IαI). In order to further establish associations of these genes with mood disorders, we evaluated behavioral phenotypes in mice deficient in either Ambp/bikunin, which is necessary for functional ITIH1 and ITIH3 complexes, or in Itih4, the gene encoding the heavy chain Itih4. We found that loss of Itih4 had no effect on the behaviors tested, but loss of Ambp/bikunin led to increased anxiety-like behavior in the light/dark and open field tests and reduced exploratory activity in the elevated plus maze, light/dark preference and open field tests. Ambp/bikunin knockout mice also exhibited a sex-dependent exaggeration of acoustic startle responses, alterations in social approach during a three-chamber choice test, and an elevated fear conditioning response. These results provide experimental support for the role of ITIH1/ITIH3 in the development of mood disorders.

摘要

近年来,多项全基因组关联研究已确定了主要情绪障碍遗传易感性的候选区域。最值得注意的是位于3号染色体p21位点的区域,该区域包含NEK4 - ITIH1 - ITIH3 - ITIH4基因。其中三个基因代表复合蛋白α-抑制因子(IαI)的重链。为了进一步确定这些基因与情绪障碍的关联,我们评估了缺乏功能性ITIH1和ITIH3复合物所必需的Ambp/ bikunin或编码重链Itih4的基因Itih4的小鼠的行为表型。我们发现,Itih4的缺失对所测试的行为没有影响,但Ambp/ bikunin的缺失导致在明暗箱和旷场试验中焦虑样行为增加,在高架十字迷宫、明暗偏好和旷场试验中探索活动减少。Ambp/ bikunin基因敲除小鼠还表现出对听觉惊吓反应的性别依赖性夸大、在三室选择试验中社交接近行为的改变以及恐惧条件反射反应增强。这些结果为ITIH1/ITIH3在情绪障碍发展中的作用提供了实验支持。

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