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高脂饮食通过下调微小RNA 140促进乳腺肌成纤维细胞分化。

A High-Fat Diet Promotes Mammary Gland Myofibroblast Differentiation through MicroRNA 140 Downregulation.

作者信息

Wolfson Benjamin, Zhang Yongshu, Gernapudi Ramkishore, Duru Nadire, Yao Yuan, Lo Pang-Kuo, Zhou Qun

机构信息

Department of Biochemistry and Molecular Biology, Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland, USA.

Department of Biochemistry and Molecular Biology, Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland, USA

出版信息

Mol Cell Biol. 2017 Feb 1;37(4). doi: 10.1128/MCB.00461-16. Print 2017 Feb 15.

Abstract

Human breast adipose tissue is a heterogeneous cell population consisting of mature white adipocytes, multipotent mesenchymal stem cells, committed progenitor cells, fibroblasts, endothelial cells, and immune cells. Dependent on external stimulation, adipose-derived stem cells differentiate along diverse lineages into adipocytes, chondrocytes, osteoblasts, fibroblasts, and myofibroblasts. It is currently not fully understood how a high-fat diet reprograms adipose-derived stem cells into myofibroblasts. In our study, we used mouse models of a regular diet and of high-fat-diet-induced obesity to investigate the role of dietary fat on myofibroblast differentiation in the mammary stromal microenvironment. We found that a high-fat diet promotes myofibroblast differentiation by decreasing microRNA 140 (miR-140) expression in mammary adipose tissue through a novel negative-feedback loop. Increased transforming growth factor β1 (TGF-β1) in mammary adipose tissue in obese mice activates SMAD3 signaling, causing phospho-SMAD3 to bind to the miR-140 locus and inhibit miR-140 transcription. This prevents miR-140 from targeting SMAD3 for degradation, resulting in amplified TGF-β1/SMAD3 signaling and miR-140 downregulation-dependent myofibroblast differentiation. Using tissue and coculture models, we found that myofibroblasts and the fibrotic microenvironment created by myofibroblasts impact the stemness and proliferation of normal ductal epithelial cells and early-stage breast cancer invasion and stemness.

摘要

人乳腺脂肪组织是一个异质性细胞群体,由成熟的白色脂肪细胞、多能间充质干细胞、定向祖细胞、成纤维细胞、内皮细胞和免疫细胞组成。脂肪来源的干细胞根据外部刺激,沿不同谱系分化为脂肪细胞、软骨细胞、成骨细胞、成纤维细胞和肌成纤维细胞。目前尚不完全清楚高脂饮食如何将脂肪来源的干细胞重编程为肌成纤维细胞。在我们的研究中,我们使用正常饮食和高脂饮食诱导肥胖的小鼠模型,来研究饮食脂肪在乳腺基质微环境中对肌成纤维细胞分化的作用。我们发现,高脂饮食通过一个新的负反馈环降低乳腺脂肪组织中微小RNA 140(miR-140)的表达,从而促进肌成纤维细胞分化。肥胖小鼠乳腺脂肪组织中转化生长因子β1(TGF-β1)增加,激活SMAD3信号通路,导致磷酸化SMAD3与miR-140基因座结合并抑制miR-140转录。这阻止了miR-140靶向SMAD3进行降解,导致TGF-β1/SMAD3信号通路放大以及依赖miR-140下调的肌成纤维细胞分化。使用组织和共培养模型,我们发现肌成纤维细胞以及由肌成纤维细胞产生的纤维化微环境会影响正常导管上皮细胞的干性和增殖,以及早期乳腺癌的侵袭和干性。

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