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