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27-羟胆固醇抑制固醇调节元件结合蛋白 1 的激活和小鼠肝脏脂质蓄积。

27-Hydroxycholesterol Inhibits Sterol Regulatory Element-Binding Protein 1 Activation and Hepatic Lipid Accumulation in Mice.

机构信息

Department of Nutrition, Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Sun Yat-sen University (Northern Campus), Guangdong Province, China.

Department of Nutrition, School of Public Health, Sun Yat-sen University (Northern Campus), Guangdong Province, China.

出版信息

Obesity (Silver Spring). 2018 Apr;26(4):713-722. doi: 10.1002/oby.22130. Epub 2018 Feb 24.

Abstract

OBJECTIVE

Although 27-hydroxycholesterol (27-HC) has been reported as a potent regulator of lipid homeostasis, its role in hepatic lipogenesis remains obscure. The present study was designed to investigate the impact of 27-HC on sterol regulatory element-binding protein 1 (SREBP-1) and hepatic steatosis.

METHODS

In this study, the 27-HC level in mice was upregulated by overexpressing CYP27A1 or treating primary hepatocytes with 27-HC, and then the hepatic lipid accumulation was detected.

RESULTS

27-HC inhibited hepatic lipid accumulation and decreased the levels of the mature active form of SREBP-1. The expression of lipogenic genes, including acetyl coenzyme A carboxylase, fatty acid synthase, stearoyl-coenzyme A desaturase-1, and glycerol-3-phosphate acyltransferase, were also suppressed after 27-HC intervention. Furthermore, 27-HC induced expression of insulin-induced gene-2 (Insig-2), an endoplasmic reticulum protein that prevents SREBP activation, both in vivo and in vitro. The inhibitory effect of 27-HC on SREBP-1 activation was absent when Insig-2 was silenced. Finally, coimmunoprecipitation showed that 27-HC promoted the binding of Insig-2 to SREBP-1.

CONCLUSIONS

These studies demonstrated the suppressive effect of 27-HC on hepatic lipid accumulation and revealed a novel mechanism by which 27-HC regulates lipogenesis.

摘要

目的

尽管 27-羟胆固醇(27-HC)已被报道为一种有效的脂质稳态调节剂,但它在肝脂肪生成中的作用仍不清楚。本研究旨在研究 27-HC 对固醇调节元件结合蛋白 1(SREBP-1)和肝脂肪变性的影响。

方法

在这项研究中,通过过表达 CYP27A1 或用 27-HC 处理原代肝细胞来上调小鼠的 27-HC 水平,然后检测肝脂质积累。

结果

27-HC 抑制肝脂质积累并降低成熟活性形式的 SREBP-1 的水平。脂生成基因的表达,包括乙酰辅酶 A 羧化酶、脂肪酸合酶、硬脂酰辅酶 A 去饱和酶-1 和甘油-3-磷酸酰基转移酶,在 27-HC 干预后也受到抑制。此外,27-HC 在体内和体外诱导胰岛素诱导基因-2(Insig-2)的表达,Insig-2 是一种阻止 SREBP 激活的内质网蛋白。当沉默 Insig-2 时,27-HC 对 SREBP-1 激活的抑制作用消失。最后,免疫共沉淀表明 27-HC 促进了 Insig-2 与 SREBP-1 的结合。

结论

这些研究表明 27-HC 对肝脂质积累具有抑制作用,并揭示了 27-HC 调节脂生成的新机制。

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