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脂肪酸结合蛋白7通过小窝蛋白-1的表达调节星形胶质细胞中小窝的功能。

Fatty acid-binding protein 7 regulates function of caveolae in astrocytes through expression of caveolin-1.

作者信息

Kagawa Yoshiteru, Yasumoto Yuki, Sharifi Kazem, Ebrahimi Majid, Islam Ariful, Miyazaki Hirofumi, Yamamoto Yui, Sawada Tomoo, Kishi Hiroko, Kobayashi Sei, Maekawa Motoko, Yoshikawa Takeo, Takaki Eiichi, Nakai Akira, Kogo Hiroshi, Fujimoto Toyoshi, Owada Yuji

机构信息

Department of Organ Anatomy, Yamaguchi University Graduate School of Medicine, Ube, Japan.

出版信息

Glia. 2015 May;63(5):780-94. doi: 10.1002/glia.22784. Epub 2015 Jan 19.

Abstract

Fatty acid-binding proteins (FABPs) bind and solubilize long-chain fatty acids, controlling intracellular lipid dynamics. FABP7 is expressed by astrocytes in the developing brain, and suggested to be involved in the control of astrocyte lipid homeostasis. In this study, we sought to examine the role of FABP7 in astrocytes, focusing on plasma membrane lipid raft function, which is important for receptor-mediated signal transduction in response to extracellular stimuli. In FABP7-knockout (KO) astrocytes, the ligand-dependent accumulation of Toll-like receptor 4 (TLR4) and glial cell-line-derived neurotrophic factor receptor alpha 1 into lipid raft was decreased, and the activation of mitogen-activated protein kinases and nuclear factor-κB was impaired after lipopolysaccharide (LPS) stimulation when compared with wild-type astrocytes. In addition, the expression of caveolin-1, not cavin-1, 2, 3, caveolin-2, and flotillin-1, was found to be decreased at the protein and transcriptional levels. FABP7 re-expression in FABP7-KO astrocytes rescued the decreased level of caveolin-1. Furthermore, caveolin-1-transfection into FABP7-KO astrocytes significantly increased TLR4 recruitment into lipid raft and tumor necrosis factor-α production after LPS stimulation. Taken together, these data suggest that FABP7 controls lipid raft function through the regulation of caveolin-1 expression and is involved in the response of astrocytes to the external stimuli. GLIA 2015;63:780-794.

摘要

脂肪酸结合蛋白(FABPs)可结合并溶解长链脂肪酸,从而控制细胞内脂质动态变化。FABP7在发育中的大脑星形胶质细胞中表达,并被认为参与星形胶质细胞脂质稳态的调控。在本研究中,我们试图研究FABP7在星形胶质细胞中的作用,重点关注质膜脂筏功能,这对于响应细胞外刺激的受体介导信号转导很重要。在FABP7基因敲除(KO)的星形胶质细胞中,与野生型星形胶质细胞相比,脂多糖(LPS)刺激后,Toll样受体4(TLR4)和胶质细胞源性神经营养因子受体α1向脂筏的配体依赖性积累减少,丝裂原活化蛋白激酶和核因子κB的激活受损。此外,在蛋白质和转录水平上,发现小窝蛋白-1(而非小窝结合蛋白-1、2、3、小窝蛋白-2和浮舰蛋白-1)的表达降低。在FABP7-KO星形胶质细胞中重新表达FABP7可挽救小窝蛋白-1水平的降低。此外,将小窝蛋白-1转染到FABP7-KO星形胶质细胞中可显著增加LPS刺激后TLR4募集到脂筏中以及肿瘤坏死因子-α的产生。综上所述,这些数据表明FABP7通过调节小窝蛋白-1的表达来控制脂筏功能,并参与星形胶质细胞对外部刺激的反应。《胶质细胞》2015年;63:780 - 794。

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