The combination of miR-122 overexpression and Let-7f silencing induces hepatic differentiation of adipose tissue-derived stem cells

被引:16
作者
Davoodian, Nahid [1 ]
Lotfi, Abbas S. [2 ]
Soleimani, Masoud [3 ]
Ghaneialvar, Hori [4 ]
机构
[1] Hormozgan Univ Med Sci, Mol Med Res Ctr, Hormozgan Hlth Inst, Bandar Abbas, Iran
[2] Tarbiat Modares Univ, Dept Clin Biochem, Fac Med Sci, Tehran, Iran
[3] Tarbiat Modares Univ, Dept Hematol, Fac Med Sci, Tehran, Iran
[4] Ilam Univ Med Sci, Sch Med, Dept Clin Biochem, Ilam, Iran
基金
美国国家科学基金会;
关键词
hepatic differentiation; hepatocyte-like cells; human adipose tissue-derived stem cells (hADSCs); let-7f; miR-122; IN-VITRO; HEPATOCYTE DIFFERENTIATION; PROGENITOR CELLS; MICRORNAS; EXPRESSION; TARGETS; VIVO;
D O I
10.1002/cbin.10836
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human adipose tissue-derived stem cells (hADSCs) have been considered as a promising source for cell therapy of liver diseases due to their accessibility, abundance, and expression of hepatocyte markers. Currently, the important role of certain microRNAs (miRNAs) has been reported during hepatic differentiation of stem cells. However, the combination effect of miRNAs on hepatic differentiation of these cells needs to be more investigated. The present study seeks to determine whether the combination of miRNAs can enhance hepatic differentiation of hADSCs in the absence of any other stimulation. First, lentiviral transduction was used to overexpress miR-122 and silence let-7f in hADSCs for up to 21 days. Then, hepatic functionality was evaluated by analyzing specific hepatocyte genes and biochemical markers at different time points of differentiation induction. Stable miR-122 overexpression and let-7f silencing together in hADSCs resulted in increased expression of hepatocyte markers including ALB, AFP, CK18, CK19, and HNF4a. In addition, urea and albumin production, immunocytochemistry, and glycogen staining confirmed that the treated cells differentiated toward hepatocyte-like cells. Therefore, our findings demonstrate the possibility of using microRNAs to induce hADSCs into functional hepatocyte-like cells.
引用
收藏
页码:1083 / 1092
页数:10
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