Chitosan/silk fibroin modified nanofibrous patches with mesenchymal stem cells prevent heart remodeling post-myocardial infarction in rats

被引:181
作者
Chen, Jiangwei [1 ,3 ,4 ]
Zhan, Yingfei [2 ]
Wang, Yabin [3 ,4 ]
Han, Dong [1 ]
Tao, Bo [3 ,4 ]
Luo, Zhenli [1 ]
Ma, Sai [1 ]
Wang, Qun [5 ]
Li, Xiang [1 ]
Fan, Li [3 ,4 ]
Li, Congye [1 ]
Deng, Hongbing [2 ]
Cao, Feng [1 ,3 ,4 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Cardiol, 169 Changle West Rd, Xian, Shaanxi, Peoples R China
[2] Wuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Hubei Key Lab Biomass Resource Chem & Environm Bi, Wuhan, Hubei, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Cardiol, 28 Fuxing Rd, Beijing, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Natl Clin Res Ctr Geriatr Dis, 28 Fuxing Rd, Beijing, Peoples R China
[5] Iowa State Univ, Dept Chem & Biol Engn, Ames, IA 50014 USA
基金
国家自然科学基金国际合作与交流项目;
关键词
Myocardial infarction; Mesenchymal stem cells; Ventricular remodeling; Stem cell nano-patch; MYOCARDIAL-INFARCTION; THERAPEUTIC-EFFICACY; MULTILAYER FILMS; STROMAL CELLS; TISSUE; FAILURE; REPAIR; SILK; EXPRESSION; EXPANSION;
D O I
10.1016/j.actbio.2018.09.013
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Poor functional survival of the engrafted stem cells limits the therapeutic efficacy of stem-cell-based therapy for myocardial infarction (MI). Cardiac patch-based system for cardiac repair has emerged as a potential regenerative strategy for MI. This study aimed to design a cardiac patch to improve the retention of the engrafted stem cells and provide mechanical scaffold for preventing the ventricular remodeling post-MI. The patches were fabricated with electrospinning cellulose nanofibers modified with chitosan/silk fibroin (CS/SF) multilayers via layer-by-layer (LBL) coating technology. The patches engineered with adipose tissue-derived mesenchymal stem cells (AD-MSCs) (cell nano-patch) were adhered to the epicardium of the infarcted region in rat hearts. Bioluminescence imaging (BLI) revealed higher cell viability in the cell nano-patch group compared with the intra-myocardial injection group. Echocardiography demonstrated less ventricular remodeling in cell nano-patch group, with a decrease in the left ventricular end-diastolic volume and left ventricular end-systolic volume compared with the control group. Additionally, left ventricular ejection fraction and fractional shortening were elevated after cell nano-patch treatment compared with the control group. Histopathological staining demonstrated that cardiac fibrosis and apoptosis were attenuated, while local neovascularization was promoted in the cell nano-patch group. Western blot analysis illustrated that the expression of biomarkers for myocardial fibrosis (TGF-beta 1, P-smad3 and Smad3) and ventricular remodeling (BNP, beta-MHC: alpha-MHC ratio) were decreased in cell nano patch-treated hearts. This study suggests that CS/SF-modified nanofibrous patches promote the functional survival of engrafted AD-MSCs and restrain ventricular remodeling post-MI through attenuating myocardial fibrosis. (C) 2018 Published by Elsevier Ltd on behalf of Acta Materialia Inc.
引用
收藏
页码:154 / 168
页数:15
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