MUSTN1和FABP3相互作用调节脂肪形成和脂质沉积。

IF 5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of Lipid Research Pub Date : 2025-05-01 Epub Date: 2025-04-15 DOI:10.1016/j.jlr.2025.100804
Yu Fu, Xin Hao, Jingru Nie, Hongliang Zhang, Peng Shang, Bo Zhang, Hao Zhang
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引用次数: 0

摘要

脂质沉积关系到农业动物生产和人类健康,阐明其分子调控机制是当前科学研究的热点和挑战。肌骨骼胚胎核蛋白1 (MUSTN1)调节生长发育,包括肌肉组织;然而,它在脂肪沉积中的作用尚不清楚。因此,我们的目标是确定这个角色。我们的新发现如下:MUSTN1在猪的脂肪组织中高表达,具有较强的脂肪沉积能力;功能上,MUSTN1促进猪和小鼠前脂肪细胞的增殖和成脂分化。MUSTN1基因敲除小鼠可防止hfd诱导的肥胖、肝脂肪变性和胰岛素抵抗;脂肪酸结合蛋白3被鉴定为MUSTN1的相互作用蛋白,通过激活磷脂酰肌醇3激酶/AKT信号通路促进前脂肪细胞增殖和分化。这项研究揭示了脂肪发育的一个积极调节因子,这为研究肥胖和通过调节MUSTN1表达的动物遗传改善提供了一种新的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MUSTN1 and FABP3 interact to regulate adipogenesis and lipid deposition.

Lipid deposition is related to agricultural animal production and human health, and elucidating its molecular regulatory mechanisms is a topic of interest and a challenge in current scientific research. Musculoskeletal embryonic nuclear protein 1 (MUSTN1) regulates growth and development, including muscle tissue; however, its role in fat deposition remains unknown. Thus, our objective was to determine this role. Our new findings were as follows: MUSTN1 was highly expressed in the fat tissue of pigs with strong adipose deposition capacity; functionally, MUSTN1 promoted the proliferation and adipogenic differentiation of porcine and mouse preadipocytes. MUSTN1 knockout mice were protected against HFD-induced obesity, hepatic steatosis, and insulin resistance; and fatty acid binding protein 3 was identified as an interacting protein of MUSTN1, which facilitated preadipocyte proliferation and differentiation by activating the phosphatidylinositol 3 kinase/AKT signaling pathways. This study reveals a positive regulator for fat development, which suggests a novel approach for studying obesity and animal genetic improvement through the modulation of MUSTN1 expression.

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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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