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首页> 外文期刊>Lipids >Short‐Chain Fatty Acids Enhance the Lipid Accumulation of 3T3‐L1 Cells by Modulating the Expression of Enzymes of Fatty Acid Metabolism
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Short‐Chain Fatty Acids Enhance the Lipid Accumulation of 3T3‐L1 Cells by Modulating the Expression of Enzymes of Fatty Acid Metabolism

机译:通过调节脂肪酸代谢酶的表达,短链脂肪酸增强了3T3-L1细胞的脂质积累

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Abstract Short‐chain fatty acids (SCFA) such as acetic acid, propionic acid, and butyric acid are produced by fermentation by gut microbiota. In this paper, we investigate the effects of SCFA on 3T3‐L1 cells and the underlying molecular mechanisms. The cells were treated with acetic acid, propionic acid, or butyric acid when cells were induced to differentiate into adipocytes. MTT assay was employed to detect the viability of 3T3‐L1 cells. Oil Red O staining was used to visualize the lipid content in 3T3‐L1 cells. A triglyceride assay kit was used to detect the triacylglycerol content in 3T3‐L1 cells. qRT‐PCR and Western blot were used to evaluate the expression of metabolic enzymes. MTT results showed that safe concentrations of acetic acid, propionic acid, and butyric acid were less than 6.4, 3.2, and 0.8 mM, respectively. Oil Red O staining and triacylglycerols detection results showed that treatment with acetic acid, propionic acid, and butyric acid accelerated the 3T3‐L1 adipocyte differentiation. qRT‐PCR and Western blot results showed that the expressions of lipoprotein lipase (LPL), adipocyte fatty acid binding protein 4 (FABP4), fatty acid transporter protein 4 (FATP4), and fatty acid synthase (FAS) were significantly increased by acetic acid, propionic acid, and butyric acid treatment during adipose differentiation ( p 0.05). In conclusion, SCFA promoted lipid accumulation by modulating the expression of enzymes of fatty acid metabolism.
机译:摘要通过肠道微生物发酵产生乙酸,丙酸和丁酸如乙酸,丙酸和丁酸等短链脂肪酸(SCFA)。在本文中,我们研究了SCFA对3T3-L1细胞和潜在的分子机制的影响。当细胞诱导细胞分化为脂肪细胞时,用乙酸,丙酸或丁酸处理细胞。 MTT测定用于检测3T3-L1细胞的活力。用于在3T3-L1细胞中可视化脂质含量的油红O染色。甘油三酯测定试剂盒用于检测3T3-L1细胞中的三酰基甘油含量。使用QRT-PCR和Western印迹来评估代谢酶的表达。 MTT结果表明,乙酸,丙酸和丁酸的安全浓度分别小于6.4,3.2和0.8mm。油红核酸染料和三酰基甘油检测结果表明,用乙酸,丙酸和丁酸处理加速3T3-L1脂肪细胞分化。 QRT-PCR和Western印迹结果表明,乙酸显着增加了脂蛋白脂肪酶(LPL),脂肪酸脂肪酸结合蛋白4(FABP4),脂肪酸转运蛋白4(FAS)和脂肪酸合酶(FAS)的表达在脂肪分化期间(P <0.05)期间,丙酸和丁酸处理。总之,通过调节脂肪酸代谢酶的表达,SCFA促进脂质积累。

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