Biomaterial-based delivery for skeletal muscle repair

被引:99
作者
Cezar, Christine A.
Mooney, David J.
机构
[1] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[2] Wyss Inst Biologically Inspired Engn, Cambridge, MA 02138 USA
关键词
Muscle regeneration; Satellite cell; Synthetic niche; Microenvironmental cue; Tissue engineered muscle; Cell therapy; Drug delivery; SATELLITE CELL ACTIVATION; STEM-CELLS; SELF-RENEWAL; MYOBLAST TRANSPLANTATION; CONNECTIVE-TISSUE; ENGINEERED MUSCLE; NICHE REGULATION; OPTIMAL TIME; REGENERATION; SCAFFOLD;
D O I
10.1016/j.addr.2014.09.008
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Skeletal muscle possesses a remarkable capacity for regeneration in response to minor damage, but severe injury resulting in a volumetric muscle loss can lead to extensive and irreversible fibrosis, scarring, and loss of muscle function. In early clinical trials, the intramuscular injection of cultured myoblasts was proven to be a safe but ineffective cell therapy, likely due to rapid death, poor migration, and immune rejection of the injected cells. In recent years, appropriate therapeutic cell types and culturing techniques have improved progenitor cell engraftment upon transplantation. Importantly, the identification of several key biophysical and biochemical cues that synergistically regulate satellite cell fate has paved the way for the development of cell-instructive biomaterials that serve as delivery vehicles for cells to promote in vivo regeneration. Material carriers designed to spatially and temporally mimic the satellite cell niche may be of particular importance for the complete regeneration of severely damaged skeletal muscle. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:188 / 197
页数:10
相关论文
共 117 条
[1]
Ali OA, 2009, SCI TRANSL MED, V1, DOI 10.1126/scitranslmed.3000359
[2]
Ali OA, 2009, NAT MATER, V8, P151, DOI [10.1038/NMAT2357, 10.1038/nmat2357]
[3]
Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis [J].
Arnold, Ludovic ;
Henry, Adeline ;
Poron, Francoise ;
Baba-Amer, Yasmine ;
van Rooijen, Nico ;
Plonquet, Anne ;
Gherardi, Romain K. ;
Chazaud, Benedicte .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (05) :1057-1069
[4]
Proinflammatory Macrophages Enhance the Regenerative Capacity of Human Myoblasts by Modifying Their Kinetics of Proliferation and Differentiation [J].
Bencze, Maximilien ;
Negroni, Elisa ;
Vallese, Denis ;
Yacoub-Youssef, Houda ;
Chaouch, Soraya ;
Wolff, Annie ;
Aamiri, Ahmed ;
Di Santo, James P. ;
Chazaud, Benedicte ;
Butler-Browne, Gillian ;
Savino, Wilson ;
Mouly, Vincent ;
Riederer, Ingo .
MOLECULAR THERAPY, 2012, 20 (11) :2168-2179
[5]
Fibronectin Regulates Wnt7a Signaling and Satellite Cell Expansion [J].
Bentzinger, C. Florian ;
Wang, Yu Xin ;
von Maltzahn, Julia ;
Soleimani, Vahab D. ;
Yin, Hang ;
Rudnicki, Michael A. ;
Rudnicki, A. .
CELL STEM CELL, 2013, 12 (01) :75-87
[6]
Mesoscopic hydrogel molding to control the 3D geometry of bioartificial muscle tissues [J].
Bian, Weining ;
Liau, Brian ;
Badie, Nima ;
Bursac, Nenad .
NATURE PROTOCOLS, 2009, 4 (10) :1522-1534
[7]
Engineered skeletal muscle tissue networks with controllable architecture [J].
Bian, Weining ;
Bursac, Nenad .
BIOMATERIALS, 2009, 30 (07) :1401-1412
[8]
Heterogeneity in the muscle satellite cell population [J].
Biressi, Stefano ;
Rando, Thomas A. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2010, 21 (08) :845-854
[9]
The Muscle Stem Cell Niche: Regulation of Satellite Cells During Regeneration [J].
Boonen, Kristel J. M. ;
Post, Mark J. .
TISSUE ENGINEERING PART B-REVIEWS, 2008, 14 (04) :419-431
[10]
Quantifying the relation between bond number and myoblast proliferation [J].
Boontheekul, Tanyarut ;
Kong, Hyun-Joon ;
Hsiong, Susan X. ;
Huang, Yen-Chen ;
Mahadevan, L. ;
Vandenburgh, Herman ;
Mooney, David J. .
FARADAY DISCUSSIONS, 2008, 139 :53-70