首页> 中文期刊> 《山东医药》 >环磷腺苷葡胺对骨髓间充质干细胞向心肌细胞分化的诱导作用及其机制探讨

环磷腺苷葡胺对骨髓间充质干细胞向心肌细胞分化的诱导作用及其机制探讨

         

摘要

Objective To investigate the mechanism of meglumine adenosine cyclophosphate ( MCA) inducing the bone marrow mesenchymal stem cells ( BMSCs ) differentiating into cardiomyocytes .Methods BMSCs were cultured in vitro, and the third generation of BMSCs were inoculated into 96 hole boards , which were then divided into the control group, MCA group and MCA +LY294002 group.The MCA group was added with 1 ×10 -3 mmol/L MCA , the MCA +LY294002 group was added with PI3K/AKT signaling pathway specific inhibitor 30 min pretreated with LY294002, and then was added with 1 ×10 -3 mmol/L MCA.After induction for 3 days, the conventional culture medium was used in the two groups to continue the culture .The control group was not treated .After 4 weeks, the mRNA expression of myocardial specific GATA gene binding protein 4 (GATA-4) and gap junction protein 43 (Cx43) was detected by fluorescence quanti-tative PCR.The expression of PI3K/AKT pathway related proteins in each group , including phosphatidylinositol 3-kinase (PI3K), serine/threonine protein kinase (Akt), a forked head transcription factor O subtype (p-Foxo3a) and the DOK family proteins (DOK5), was detected by Western blotting.Results The expression of GATA-4 and CX43 mRNA in the MCA group and MCA +LY294002 group was higher than that of the control group (all P<0.01), the expression of GA-TA-4 and CX43 mRNA in the MCA +LY294002 group was lower than that in the MCA group ( all P<0 .01 ) .The ex-pression of PI3K, p-AKT, p-Foxo3a and DOK5 in the MCA group was higher than that in the control group and MCA +LY294002 group (all P<0.01).Conclusion MCA can induce BMSCs differentiating into cardiomyocytes , and its mech-anism may be related to the activation of PI3K/AKT signaling pathway.%目的:探讨环磷腺苷葡胺(MCA)诱导骨髓间充质干细胞(BMSCs)向心肌细胞分化的机制。方法体外培养BMSCs,将第3代BMSCs接种于96孔板中,分为对照组、MCA组、MCA+LY294002组。 MCA组加入1×10-3 mmol/L的MCA,MCA+LY294002组加PI3K/AKT信号通路特异性抑制剂LY294002预处理30 min后,再加入1×10-3 mmol/L的MCA,两组均诱导3 d后换为普通培养基继续培养。对照组不做任何处理。培养4周后,采用荧光定量PCR法检测心肌特异性基因GATA结合蛋白4(GATA-4)、缝隙连接蛋白43(CX43) mRNA,采用Western blot法检测PI3K/AKT通路相关蛋白PI3K、磷酸化AKT(p-AKT)、磷酸化叉形头转录因子的O亚型(p-Foxo3a)、DOK家族蛋白(DOK5)]的表达。结果 MCA组、MCA+LY294002组GATA-4、CX43 mRNA表达均高于对照组(P均<0.01),MCA+LY294002组 GATA-4、CX43 mRNA 表达均低于MCA 组(P 均<0.01)。 MCA 组 PI3K、p-AKT、p-Foxo3a、DOK5表达均高于对照组及MCA+LY294002组(P均<0.01)。结论 MCA可诱导BMSCs分化为心肌细胞,其机制可能与激活PI3 K/AKT信号通路有关。

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