Promotion of cardiac differentiation of brown adipose derived stem cells by chitosan hydrogel for repair after myocardial infarction

被引:123
|
作者
Wang, Haibin [1 ]
Shi, Jinxin [2 ,3 ]
Wang, Yan [1 ]
Yin, Yujing [4 ]
Wang, Liman [1 ]
Liu, Jianfeng [2 ]
Liu, Zhiqiang [1 ]
Duan, Cuimi [1 ]
Zhu, Ping [2 ]
Wang, Changyong [1 ]
机构
[1] Acad Mil Med Sci, Inst Basic Med Sci, Dept Adv Interdisciplinary Studies, Tissue Engn Res Ctr, Beijing 100850, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Cardiovasc Dept, Beijing 100853, Peoples R China
[3] Capital Med Univ, Shijingshan Teaching Hosp, Beijing Shijingshan Hosp, Beijing 100043, Peoples R China
[4] Acad Mil Med Sci, Inst Transfus Med, Beijing 100850, Peoples R China
基金
中国国家自然科学基金; 国家自然科学基金国际合作与交流项目; 国家杰出青年科学基金;
关键词
Chitosan hydrogel; Adipose derived stem cell; Brown adipose tissue; Myocardial infarction; Tissue engineering; PROGENITOR CELLS; TRANSPLANTATION; TISSUE; HEARTS; MOUSE; WHITE; CARDIOMYOCYTES; ANGIOGENESIS; PERFORMANCE; ADIPOCYTES;
D O I
10.1016/j.biomaterials.2014.01.021
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The ability to restore heart function by replacement of diseased myocardium is one of the great challenges in biomaterials and regenerative medicine. Brown adipose derived stem cells (BADSCs) present a new source of cardiomyocytes to regenerate the myocardium after infarction. In this study, we explored an injectable tissue engineering strategy to repair damaged myocardium, in which chitosan hydrogels were investigated as a carrier for BADSCs. In vitro, the effect and mechanism of chitosan components on the cardiac differentiation of BADSCs were investigated. In vivo, BADSCs carrying double-fusion reporter gene (firefly luciferase and monomeric red fluorescent protein (fluc-mRFP)) were transplanted into infarcted rat hearts with or without chitosan hydrogel. Multi-techniques were used to assess the effects of treatments. We observed that chitosan components significantly enhanced cardiac differentiation of BADSCs, which was assessed by percentages of cTnT(+) cells and expression of cardiac-specific markers, including GATA-4, Nkx2.5, My17, Myh6, cTnI, and Cacnala. Treatment with collagen synthesis inhibitors, cis-4-hydroxy-D-proline (CIS), significantly inhibited the chitosan-enhanced cardiac differentiation, indicating that the enhanced collagen synthesis by chitosan accounts for its promotive role in cardiac differentiation of BADSCs. Longitudinal in vivo bioluminescence imaging and histological staining revealed that chitosan enhanced the survival of engrafted BADSCs and significantly increased the differentiation rate of BADSCs into cardiomyocytes in vivo. Furthermore, BADSCs delivered by chitosan hydrogel prevented adverse matrix remodeling, increased angiogenesis, and preserved heart function. These results suggested that the injectable cardiac tissue engineering based on chitosan hydrogel and BADSCs is a useful strategy for myocardium regeneration. (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3986 / 3998
页数:13
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