The role of multifunctional delivery scaffold in the ability of cultured myoblasts to promote muscle regeneration

被引:108
作者
Borselli, Cristina [1 ,2 ,3 ]
Cezar, Christine A. [1 ,2 ]
Shvartsman, Dymitri [1 ,2 ]
Vandenburgh, Herman H. [4 ]
Mooney, David J. [1 ,2 ]
机构
[1] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[2] Harvard Univ, Div Engn & Appl Sci, Wyss Inst, Cambridge, MA 02138 USA
[3] Univ Naples Federico II, Dept Mat Engn & Prod, Naples, Italy
[4] Myomics Inc, Providence, RI USA
基金
美国国家卫生研究院;
关键词
Hydrogel; Alginate; Drug delivery; Cell activation; Muscle; BONE-MARROW; STEM-CELLS; SKELETAL-MUSCLE; GROWTH; FIBER; POPULATION; HYDROGELS; ISOFORM; MICE;
D O I
10.1016/j.biomaterials.2011.08.019
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Many cell types of therapeutic interest, including myoblasts, exhibit reduced engraftment if cultured prior to transplantation. This study investigated whether polymeric scaffolds that direct cultured myoblasts to migrate outwards and repopulate the host damaged tissue, in concert with release of angiogenic factors designed to enhance revascularizaton of the regenerating tissue, would enhance the efficacy of this cell therapy and lead to functional muscle regeneration. This was investigated in the context of a severe injury to skeletal muscle tissue involving both myotoxin-mediated direct damage and induction of regional ischemia. Local and sustained release of VEGF and IGF-1 from macroporous scaffolds used to transplant and disperse cultured myogenic cells significantly enhanced their engraftment, limited fibrosis, and accelerated the regenerative process. This resulted in increased muscle mass and, improved contractile function. These results demonstrate the importance of finely controlling the microenvironment of transplanted cells in the treatment of severe muscle damage. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8905 / 8914
页数:10
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