Engineering vascularized skeletal muscle tissue

被引:930
作者
Levenberg, S
Rouwkema, J
Macdonald, M
Garfein, ES
Kohane, DS
Darland, DC
Marini, R
van Blitterswijk, CA
Mulligan, RC
D'Amore, PA
Langer, R [1 ]
机构
[1] Technion Israel Inst Technol, Dept Biomed Engn, IL-32000 Haifa, Israel
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[3] MIT, Div Comparat Med, Cambridge, MA 02139 USA
[4] Univ Twente, Inst Biomed Technol, NL-3723 MB Bilthoven, Netherlands
[5] Brigham & Womens Hosp, Dept Surg, Boston, MA 02115 USA
[6] Massachusetts Gen Hosp, Dept Pediat, Boston, MA 02114 USA
[7] Schepens Eye Res Inst, Boston, MA 02114 USA
[8] Dept Ophthalmol, Boston, MA 02114 USA
[9] Harvard Univ, Sch Med, Dept Mol Med, Childrens Hosp, Boston, MA 02115 USA
关键词
D O I
10.1038/nbt1109
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
One of the major obstacles in engineering thick, complex tissues such as muscle is the need to vascularize the tissue in vitro. Vascularization in vitro could maintain cell viability during tissue growth, induce structural organization and promote vascularization upon implantation. Here we describe the induction of endothelial vessel networks in engineered skeletal muscle tissue constructs using a three-dimensional multiculture system consisting of myoblasts, embryonic fibroblasts and endothelial cells coseeded on highly porous, biodegradable polymer scaffolds. Analysis of the conditions for induction and stabilization of the vessels in vitro showed that addition of embryonic fibroblasts increased the levels of vascular endothelial growth factor expression in the construct and promoted formation and stabilization of the endothelial vessels. We studied the survival and vascularization of the engineered muscle implants in vivo in three different models. Prevascularization improved the vascularization, blood perfusion and survival of the muscle tissue constructs after transplantation.
引用
收藏
页码:879 / 884
页数:6
相关论文
共 28 条
[1]   Engineering of muscle tissue [J].
Bach, AD ;
Stern-Straeter, J ;
Beier, JP ;
Bannasch, H ;
Stark, GB .
CLINICS IN PLASTIC SURGERY, 2003, 30 (04) :589-+
[2]   In vitro reconstruction of a human capillary-like network in a tissue-engineered skin equivalent [J].
Black, AF ;
Berthod, F ;
L'Heureux, N ;
Germain, L ;
Auger, FA .
FASEB JOURNAL, 1998, 12 (13) :1331-1340
[3]   PLASTICITY OF THE DIFFERENTIATED STATE [J].
BLAU, HM ;
PAVLATH, GK ;
HARDEMAN, EC ;
CHIU, CP ;
SILBERSTEIN, L ;
WEBSTER, SG ;
MILLER, SC ;
WEBSTER, C .
SCIENCE, 1985, 230 (4727) :758-766
[4]   Skeletal muscle formation in vertebrates [J].
Buckingham, M .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2001, 11 (04) :440-448
[5]   Angiogenesis in health and disease [J].
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (06) :653-660
[6]   TGFβ is required for the formation of capillary-like structures in three-dimensional cocultures of 10T1/2 and endothelial cells [J].
Darland D.C. ;
D'amore P.A. .
Angiogenesis, 2001, 4 (1) :11-20
[7]   Pericyte production of cell-associated VEGF is differentiation-dependent and is associated with endothelial survival [J].
Darland, DC ;
Massingham, LJ ;
Smith, SR ;
Piek, E ;
St-Geniez, M ;
D'Amore, PA .
DEVELOPMENTAL BIOLOGY, 2003, 264 (01) :275-288
[8]  
Flamme I, 1997, J CELL PHYSIOL, V173, P206, DOI 10.1002/(SICI)1097-4652(199711)173:2<206::AID-JCP22>3.0.CO
[9]  
2-C
[10]   PDGF, TGF-β, and heterotypic cell-cell interactions mediate endothelial cell-induced recruitment of 10T1/2 cells and their differentiation to a smooth muscle fate [J].
Hirschi, KK ;
Rohovsky, SA ;
D'Amore, PA .
JOURNAL OF CELL BIOLOGY, 1998, 141 (03) :805-814