Wang Liang, Xu Lei, Xu Min, Liu Guoqiang, Xing Jian, Sun Caifeng, Ding Huifang
Shengli Oilfield Central Hospital, Dongying, Shandong, P.R. China.
Cell Physiol Biochem. 2015;35(6):2285-98. doi: 10.1159/000374032. Epub 2015 Apr 13.
BACKGROUND/AIMS: The elucidation of the molecular mechanism of adipocyte differentiation in mesenchymal stem cells is of essential importance for the development of treatments for metabolic diseases, such as obesity and diabetes.
The expression levels of miR-342-3p and carboxy-terminal binding protein 2 (CtBP2) were regulated by oligonucleotide transfection. Adipogenic differentiation was induced by adipogenic medium containing indomethacin, dexamethasone and 3-isobutyl-1-methylxanthine on day 12, as determined by Oil Red O staining and triglyceride concentration assay to assess intracellular lipid accumulation. The induction of adipocyte-specific transcription factors and markers was detected by qRT-PCR and western blot. The regulation of CtBP2 expression by miR-342-3p was determined by western blot, qRT-PCR, luciferase reporter assay, ChIP assay and functional experiments.
We revealed that miR-342-3p was enriched in the adipose tissue of obese mice, and its expression was significantly elevated during adipogenic differentiation in both human mesenchymal stem cells (hMSCs) and 3T3L1 cells. Using gain- and loss-of-function assays, we demonstrated that the overexpression of miR-342-3p markedly promoted the differentiation of hMSCs into an adipogenic lineage. Adipogenesis was significantly blocked by miR-342-3p downregulation. We identified and validated that CtBP2 was a direct target of miR-342-3p in this process. The effects of the inhibition of CtBP2 were similar to those of miR-342-5p overexpression on adipogenic differentiation, promoting the release of C/EBPα from CtBP2 binding.
miR-342-3p is a powerful enhancer of the adipogenesis of human adipose-derived MSCs that acts by inhibiting CtBP2 and releasing the key adipogenic regulator C/EBPα from CtBP2 binding, subsequently activating the expression of adipogenic transcription factors and markers.
背景/目的:阐明间充质干细胞中脂肪细胞分化的分子机制对于开发肥胖和糖尿病等代谢性疾病的治疗方法至关重要。
通过寡核苷酸转染调节miR-342-3p和羧基末端结合蛋白2(CtBP2)的表达水平。在第12天,用含有消炎痛、地塞米松和3-异丁基-1-甲基黄嘌呤的成脂培养基诱导成脂分化,通过油红O染色和甘油三酯浓度测定来评估细胞内脂质积累。通过qRT-PCR和蛋白质免疫印迹法检测脂肪细胞特异性转录因子和标志物的诱导情况。通过蛋白质免疫印迹法、qRT-PCR、荧光素酶报告基因测定、染色质免疫沉淀测定和功能实验确定miR-342-3p对CtBP2表达的调节作用。
我们发现miR-342-3p在肥胖小鼠的脂肪组织中富集,并且在人骨髓间充质干细胞(hMSCs)和3T3L1细胞的成脂分化过程中其表达显著升高。使用功能获得和功能丧失实验,我们证明miR-342-3p的过表达显著促进hMSCs向脂肪生成谱系的分化。miR-342-3p下调显著阻断了脂肪生成。我们鉴定并验证CtBP2在此过程中是miR-342-3p的直接靶标。抑制CtBP2的作用与miR-342-5p过表达对成脂分化的作用相似,促进C/EBPα从CtBP2结合中释放。
miR-3�2-3p是人类脂肪来源的间充质干细胞成脂作用的强大增强剂,其作用机制是抑制CtBP2并使关键的成脂调节因子C/EBPα从CtBP2结合中释放,随后激活成脂转录因子和标志物的表达。