Gene Expression Profiling in the Cortex of Fabp4 Knockout Mice.

IF 2 Q3 NEUROSCIENCES
Hinako Kirikae, Xiaofeng He, Tetsuo Ohnishi, Hirofumi Miyazaki, Takeo Yoshikawa, Yuji Owada, Motoko Maekawa
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引用次数: 0

Abstract

Aims: Fatty acid binding protein 4, adipocyte (Fabp4), is well known for its role in peripheral lipid metabolism, but its potential role in brain function remains largely unexplored. This study aimed to investigate Fabp4 expression in the adult mouse brain and explore gene expression changes in Fabp4 knockout (KO) mice to assess its potential impact on brain function.

Methods: We conducted in situ hybridization to assess Fabp4 expression in key brain regions of adult mice. In parallel, differential gene expression analysis using RNA-seq was conducted in the prefrontal cortex of Fabp4 KO mice to identify genes affected by Fabp4 deficiency.

Results: No Fabp4 expression was detected in the brains of mice, suggesting a lack of direct involvement in the central nervous system. However, Fabp4 KO mice exhibited significant changes in gene expression in the brain, with 31 genes upregulated and 30 downregulated. Downregulated genes were linked to histone methylation and metabolic processes, while upregulated ones were associated with synaptic organization.

Conclusion: Although Fabp4 is not expressed in the brain, its deficiency leads to substantial changes in gene expression, likely mediated by peripheral metabolic pathways and epigenetic regulation. These changes may explain the previously observed autism-like behaviors and increased dendritic spine density in Fabp4 KO mice. This study sheds light on the role of systemic lipid metabolism in neurodevelopmental disorders such as autism spectrum disorder (ASD) and highlights epigenetic mechanisms as potential mediators of these effects.

Fabp4基因敲除小鼠皮层基因表达谱分析。
目的:脂肪酸结合蛋白4,脂肪细胞(Fabp4),众所周知其在外周脂质代谢中的作用,但其在脑功能中的潜在作用仍未被充分探索。本研究旨在研究Fabp4在成年小鼠脑中的表达,探讨Fabp4敲除(KO)小鼠的基因表达变化,以评估其对脑功能的潜在影响。方法:采用原位杂交法检测Fabp4在成年小鼠脑关键区域的表达。同时,利用RNA-seq对Fabp4 KO小鼠前额皮质进行差异基因表达分析,以鉴定Fabp4缺陷影响的基因。结果:小鼠大脑中未检测到Fabp4的表达,提示其不直接参与中枢神经系统。然而,Fabp4 KO小鼠在大脑中表现出明显的基因表达变化,31个基因上调,30个基因下调。下调的基因与组蛋白甲基化和代谢过程有关,而上调的基因与突触组织有关。结论:虽然Fabp4在大脑中不表达,但其缺乏导致基因表达发生实质性变化,可能通过外周代谢途径和表观遗传调控介导。这些变化可以解释先前观察到的Fabp4 KO小鼠的自闭症样行为和增加的树突棘密度。本研究揭示了全身脂质代谢在自闭症谱系障碍(ASD)等神经发育障碍中的作用,并强调了表观遗传机制作为这些影响的潜在介质。
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
Neuropsychopharmacology Reports
Neuropsychopharmacology Reports Psychology-Clinical Psychology
CiteScore
3.60
自引率
4.00%
发文量
75
审稿时长
14 weeks
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