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脂肪酸结合蛋白7通过与星形胶质细胞核中的ATP柠檬酸裂解酶相互作用来调节乙酰辅酶A代谢。

FABP7 Regulates Acetyl-CoA Metabolism Through the Interaction with ACLY in the Nucleus of Astrocytes.

作者信息

Kagawa Yoshiteru, Umaru Banlanjo Abdulaziz, Shima Hiroki, Ito Ryo, Zama Ryo, Islam Ariful, Kanno Shin-Ichiro, Yasui Akira, Sato Shun, Jozaki Kosuke, Shil Subrata Kumar, Miyazaki Hirofumi, Kobayashi Shuhei, Yamamoto Yui, Kogo Hiroshi, Shimamoto-Mitsuyama Chie, Sugawara Akira, Sugino Norihiro, Kanamori Masayuki, Tominaga Teiji, Yoshikawa Takeo, Fukunaga Kohji, Igarashi Kazuhiko, Owada Yuji

机构信息

Department of Organ Anatomy, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.

Department of Biochemistry, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.

出版信息

Mol Neurobiol. 2020 Dec;57(12):4891-4910. doi: 10.1007/s12035-020-02057-3. Epub 2020 Aug 19.

Abstract

Fatty acid binding protein 7 (FABP7) is an intracellular fatty acid chaperon that is highly expressed in astrocytes, oligodendrocyte-precursor cells, and malignant glioma. Previously, we reported that FABP7 regulates the response to extracellular stimuli by controlling the expression of caveolin-1, an important component of lipid raft. Here, we explored the detailed mechanisms underlying FABP7 regulation of caveolin-1 expression using primary cultured FABP7-KO astrocytes as a model of loss of function and NIH-3T3 cells as a model of gain of function. We discovered that FABP7 interacts with ATP-citrate lyase (ACLY) and is important for acetyl-CoA metabolism in the nucleus. This interaction leads to epigenetic regulation of several genes, including caveolin-1. Our novel findings suggest that FABP7-ACLY modulation of nuclear acetyl-CoA has more influence on histone acetylation than cytoplasmic acetyl-CoA. The changes to histone structure may modify caveolae-related cell activity in astrocytes and tumors, including malignant glioma.

摘要

脂肪酸结合蛋白7(FABP7)是一种细胞内脂肪酸伴侣蛋白,在星形胶质细胞、少突胶质前体细胞和恶性胶质瘤中高度表达。此前,我们报道FABP7通过控制脂筏的重要组成部分小窝蛋白-1的表达来调节对细胞外刺激的反应。在此,我们以原代培养的FABP7基因敲除星形胶质细胞作为功能丧失模型,以NIH-3T3细胞作为功能获得模型,探索FABP7调节小窝蛋白-1表达的详细机制。我们发现FABP7与ATP-柠檬酸裂解酶(ACLY)相互作用,并且对细胞核中的乙酰辅酶A代谢很重要。这种相互作用导致包括小窝蛋白-1在内的多个基因的表观遗传调控。我们的新发现表明,FABP7-ACLY对细胞核乙酰辅酶A的调节比对细胞质乙酰辅酶A对组蛋白乙酰化的影响更大。组蛋白结构的变化可能会改变星形胶质细胞和肿瘤(包括恶性胶质瘤)中与小窝相关的细胞活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa81/7541391/00c7c10ef7d3/12035_2020_2057_Fig1_HTML.jpg

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