端粒酶
MAPK/ERK通路
间充质干细胞
细胞生物学
脂肪细胞
间质细胞
信号转导
癌症研究
生物
化学
脂肪组织
内分泌学
遗传学
基因
作者
Sara Sultan Alomran,Muhammad Nasir Khan Khattak,Amir Ali Khan,Sallam Hasan Abdallah,Abeer Maher Fayyad,Khalid Bajou
标识
DOI:10.17582/journal.pjz/20191127131153
摘要
Unraveling molecular mechanisms that govern adipocyte formation will lead to a greater understanding of obesity and subsequent treatment.In the current study, we assessed the effects of miR-22-3p, a non-coding RNA, on adipocyte differentiation from telomerase-transformed Mesenchymal Stromal Cells (iMSC3).The transfection of iMSC3 with miR-22-3p suppressed adipocyte differentiation as evident by reduction in lipid content and number of lipid droplets.While AKT3 is reported to be a target of miR-22-3p, our study indicated otherwise.Moreover, while miR-22-3p is known to target more than 500 genes, MAPK has not been identified as one of the more than 500 gene targets of miR-22-3p, though this pathway was upregulated in transfected iMSC3 that differentiated to adipocytes.Finally, miR-22-3p was observed to suppress adipocytes and was involved in adipocyte differentiation through non-targeted MAPK pathway upregulation rather than AKT3-related processes.
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