肝羧酸酯酶3 (CES3)的丧失可阻止小鼠MASLD的发展。

IF 4.1 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zaid Batayneh, Xiaoli Pan, Raja Gopoju, Shuwei Hu, Shaoyu Chen, Jiayou Wang, Hui Wang, Lakshitha Gunawardana, Takhar Kasumov, Yanqiao Zhang
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引用次数: 0

摘要

羧酸酯酶(CES)是代谢具有酯、硫酯和酰胺键的化合物所必需的。虽然CES1和CES2在脂质代谢中的作用已经很好地确立,但CES3在脂质代谢或代谢功能障碍相关的脂肪变性肝病(MASLD)中的作用知之甚少。在这里,我们报道了CES3的定位和营养调节及其在小鼠MASLD发展中的作用。CES3仅在肝脏中表达,并定位于内质网(ER)。代谢功能障碍相关脂肪性肝炎(MASH)患者和饲喂西方饮食的小鼠肝脏CES3降低。出乎意料的是,CES3的缺失减轻了西方饮食诱导的MASLD,而人类肝脏特异性CES3的过表达加重了西方饮食诱导的MASLD。从机制上讲,CES3的损失减少了脂肪的重新生成,并促进了极低密度脂蛋白(VLDL) -甘油三酯的分泌。因此,目前的研究已经确定了CES3在肝脏脂质代谢和MASLD中的新作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Loss of hepatic carboxylesterase 3 prevents the development of MASLD in mice.

Carboxylesterases (CESs) are essential for metabolizing compounds with ester, thioester, and amide bonds. While the roles of CES1 and CES2 in lipid metabolism have been well established, little is known about the role of CES3 in lipid metabolism or metabolic dysfunction-associated steatotic liver disease (MASLD). Here, we report the localization and nutritional regulation of CES3 and its role in MASLD development in mice. CES3 is expressed exclusively in the liver and localizes to the ER. Hepatic CES3 is reduced in patients with metabolic dysfunction-associated steatohepatitis and mice fed a Western diet. Unexpectedly, loss of CES3 alleviates Western diet-induced MASLD, whereas liver-specific overexpression of human CES3 worsens Western diet-induced MASLD. Mechanistically, loss of CES3 reduces de novo lipogenesis and promotes the secretion of VLDL-triglycerides. Thus, the current study has identified a novel role of CES3 in hepatic lipid metabolism and MASLD.

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来源期刊
Journal of Lipid Research
Journal of Lipid Research 生物-生化与分子生物学
CiteScore
11.10
自引率
4.60%
发文量
146
审稿时长
41 days
期刊介绍: The Journal of Lipid Research (JLR) publishes original articles and reviews in the broadly defined area of biological lipids. We encourage the submission of manuscripts relating to lipids, including those addressing problems in biochemistry, molecular biology, structural biology, cell biology, genetics, molecular medicine, clinical medicine and metabolism. Major criteria for acceptance of articles are new insights into mechanisms of lipid function and metabolism and/or genes regulating lipid metabolism along with sound primary experimental data. Interpretation of the data is the authors’ responsibility, and speculation should be labeled as such. Manuscripts that provide new ways of purifying, identifying and quantifying lipids are invited for the Methods section of the Journal. JLR encourages contributions from investigators in all countries, but articles must be submitted in clear and concise English.
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