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骨髓间充质干细胞移植后大鼠缺血心肌的超微结构变化

[Ultrastructural changes of rat ischemic myocardium after bone marrow mesenchymal stem cell transplantation].

作者信息

Jiang Wen-hui, Ma Ai-qun, Han Ke, Liu Yu, Wang Ting-zhong, Zheng Xiao-pu, Wang Jun

机构信息

Department of Cardiology, First Hospital of Xi'an Jiaotong University, Key Laboratory of Environment and Genes related Diseases of Ministry of Education, Xi'an 710061, China.

出版信息

Di Yi Jun Yi Da Xue Xue Bao. 2005 Sep;25(9):1090-4.

Abstract

OBJECTIVE

To observe the ultrastructural changes of ischemic myocardium of rats after bone marrow mesenchymal stem cells (MSCs) transplantation.

METHODS

Rat models of myocardial ischemia were established by ligating the descending anterior branch of the left coronary artery. The isolated and in vitro cultured MSCs labeled with 4' 6-diamidine-2-phenylindole (DAPI) were injected into the rats via the tail vein and the hearts of the rats were taken 1 week and 8 weeks after transplantation, respectively, for observation under fluorescence microscopy. The ultrastructural changes of the ischemic myocardium of the recipient rats were observed by transmission electron microscope.

RESULTS

The third passage of cultured MSCs growing in colonies possessed good homogeneity. One week and 8 weeks after transplantation, DAPI-labeled cells were observed in the heart of the recipient rats, but not in the hearts of control rats. One week after transplantation, ultrastructural observation identified a small number of cells in the peripherals of the infarct area of the recipient rats with similar morphology to that of MSCs cultured in vitro. At 8 weeks,a large number of capillaries were seen in the ischemic myocardium on the peripheral of the infarct area. Ultrastructural observation also revealed some immature myocytes surviving in the ischemic region.

CONCLUSION

MSCs is capable in vivo of homing to the ischemic myocardium via the blood circulation, and promote regeneration of the myocardium and blood vessels.

摘要

目的

观察骨髓间充质干细胞(MSCs)移植后大鼠缺血心肌的超微结构变化。

方法

通过结扎左冠状动脉前降支建立大鼠心肌缺血模型。将经4',6-二脒基-2-苯基吲哚(DAPI)标记的体外分离培养的MSCs经尾静脉注入大鼠体内,分别于移植后1周和8周取大鼠心脏,进行荧光显微镜观察。用透射电子显微镜观察受体大鼠缺血心肌的超微结构变化。

结果

培养的第3代MSCs呈集落生长,均一性良好。移植后1周和8周,在受体大鼠心脏中观察到DAPI标记的细胞,而在对照大鼠心脏中未观察到。移植后1周,超微结构观察发现受体大鼠梗死灶周边有少量细胞,其形态与体外培养的MSCs相似。8周时,梗死灶周边缺血心肌中有大量毛细血管。超微结构观察还显示缺血区域有一些存活的未成熟心肌细胞。

结论

MSCs在体内能够通过血液循环归巢至缺血心肌,促进心肌和血管再生。

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