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溶血磷脂酰肌醇酰基转移酶-1参与巨噬细胞胞质钙振荡。

Lysophosphatidylinositol-acyltransferase-1 is involved in cytosolic Ca oscillations in macrophages.

作者信息

Takemasu Shinya, Ito Masaaki, Morioka Shin, Nigorikawa Kiyomi, Kofuji Satoshi, Takasuga Shunsuke, Eguchi Satoshi, Nakanishi Hiroki, Matsuoka Isao, Sasaki Junko, Sasaki Takehiko, Hazeki Kaoru

机构信息

Graduate School of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.

Laboratory of Pharmacology, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Japan.

出版信息

Genes Cells. 2019 May;24(5):366-376. doi: 10.1111/gtc.12681. Epub 2019 Apr 16.

Abstract

Lysophosphatidylinositol-acyltransferase-1 (LPIAT1) specifically catalyzes the transfer of arachidonoyl-CoA to lysophosphoinositides. LPIAT mice have been shown to have severe defects in the brain and liver; however, the exact molecular mechanisms behind these conditions are not well understood. As immune cells have been implicated in liver inflammation based on disfunction of LPIAT1, we generated Raw264.7 macrophages deficient in LPIAT1, using shRNA and CRISPR/Cas9. The amount of C38:4 species in phosphoinositides, especially in PtdInsP , was remarkably decreased in these cells. Unlike in wild-type cells, LPIAT1-deficient cells showed prolonged oscillations of intracellular Ca upon UDP stimulation, which is known to activate phospholipase Cβ through the Gq-coupled P2Y6 receptor, even in the absence of extracellular Ca . It is speculated that the prolonged Ca response may be relevant to the increased risk of liver inflammation induced by LPIAT1 disfunction.

摘要

溶血磷脂酰肌醇-酰基转移酶-1(LPIAT1)特异性催化花生四烯酰辅酶A向溶血磷脂酰肌醇的转移。已证明LPIAT基因敲除小鼠在脑和肝脏中存在严重缺陷;然而,这些情况背后的确切分子机制尚不清楚。由于基于LPIAT1功能障碍,免疫细胞与肝脏炎症有关,我们使用shRNA和CRISPR/Cas9技术构建了LPIAT1缺陷的Raw264.7巨噬细胞。这些细胞中磷酸肌醇尤其是磷脂酰肌醇磷酸中C38:4种类的含量显著降低。与野生型细胞不同,LPIAT1缺陷细胞在UDP刺激后表现出细胞内钙离子的延长振荡,已知UDP通过Gq偶联的P2Y6受体激活磷脂酶Cβ,即使在没有细胞外钙离子的情况下也是如此。据推测,延长的钙离子反应可能与LPIAT1功能障碍引起的肝脏炎症风险增加有关。

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