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促红细胞生成素通过激活ERK和P38 MAPK抑制骨髓间充质干细胞的脂肪生成分化

Inhibition of adipogenic differentiation of bone marrow mesenchymal stem cells by erythropoietin via activating ERK and P38 MAPK.

作者信息

Liu G X, Zhu J C, Chen X Y, Zhu A Z, Liu C C, Lai Q, Chen S T

机构信息

Hematology Institute of Ji'nan University, Guangzhou City,Guangdong Province, China.

Hematology Institute of Ji'nan University, Guangzhou City,Guangdong Province, China

出版信息

Genet Mol Res. 2015 Jun 26;14(2):6968-77. doi: 10.4238/2015.June.26.5.

Abstract

We examined whether erythropoietin (EPO) can inhibit adipogenic differentiation of mesenchymal stem cells (MSCs) in the mouse bone marrow and its underlying mechanism. We separated and extracted mouse bone marrow MSCs and induced adipogenic differen-tiation using 3-isobutyl-1-methylxanthine, insulin, and dexamethasone. Different concentrations of EPO were added to the cells and observed by Oil Red O staining on the 20th day to quantitatively analyze the degree of cell differentiation. mRNA expression levels of peroxysome proliferator-activated receptor γ (PPARγ), CCAAT enhancer binding protein α, and adiponectin were analyzed by real-time quantitative polymerase chain reaction, and the activity of PPARγ, extracellular sig-nal-regulated kinase (ERK), and p38 mitogen-activated protein kinase (p38 MAPK) were determined by western blotting. EPO significantly inhibited adipogenic differentiation of MSCs after 20 days and reduced absorbance values by Oil Red O staining without affecting proliferation activity. EPO downregulated the mRNA expression of PPARγ, CCAAT enhancer binding protein α, fatty acid binding protein 4, and adiponec-tin during adipogenesis and increased protein phosphorylation of ERK, p38 MAPK, and PPARγ during differentiation. EPO downregulated the mRNA expression of PPARγ, CCAAT enhancer binding protein α, fatty acid binding protein 4, and adiponectin by increasing protein phosphor-ylation of ERK, p38 MAPK, and PPARγ during differentiation, which inhibited adipogenic differentiation of MSCs.

摘要

我们研究了促红细胞生成素(EPO)是否能抑制小鼠骨髓间充质干细胞(MSCs)的成脂分化及其潜在机制。我们分离并提取了小鼠骨髓间充质干细胞,使用3-异丁基-1-甲基黄嘌呤、胰岛素和地塞米松诱导其成脂分化。向细胞中添加不同浓度的EPO,并在第20天通过油红O染色观察,以定量分析细胞分化程度。通过实时定量聚合酶链反应分析过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT增强子结合蛋白α和脂联素的mRNA表达水平,并通过蛋白质印迹法测定PPARγ、细胞外信号调节激酶(ERK)和p38丝裂原活化蛋白激酶(p38 MAPK)的活性。20天后,EPO显著抑制了间充质干细胞的成脂分化,并通过油红O染色降低了吸光度值,而不影响增殖活性。EPO在脂肪生成过程中下调了PPARγ、CCAAT增强子结合蛋白α、脂肪酸结合蛋白4和脂联素的mRNA表达,并在分化过程中增加了ERK、p38 MAPK和PPARγ的蛋白磷酸化。EPO通过在分化过程中增加ERK、p38 MAPK和PPARγ的蛋白磷酸化,下调了PPARγ、CCAAT增强子结合蛋白α、脂肪酸结合蛋白4和脂联素的mRNA表达,从而抑制了间充质干细胞的成脂分化。

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