Human tissue-engineered blood vessels for adult arterial revascularization

被引:695
作者
L'Heureux, N
Dusserre, N
Konig, G
Victor, B
Keire, P
Wight, TN
Chronos, NAF
Kyles, AE
Gregory, CR
Hoyt, G
Robbins, RC
McAllister, TN
机构
[1] Cytograft Tissue Engn Inc, Novato, CA 94949 USA
[2] Capitol Cardiovasc Imaging Ctr, Sacramento, CA 95816 USA
[3] Benaroya Res Inst Virginia Mason, Hope Heart Program, Seattle, WA 98101 USA
[4] Amer Cardiovasc Res Inst, Atlanta, GA 30342 USA
[5] Univ Calif Davis, Dept Surg & Radiol Sci, Sch Vet Med, Davis, CA 95616 USA
[6] Stanford Univ, Dept Cardiothorac Surg, Falk Cardiovasc Res Ctr, Stanford, CA 94305 USA
关键词
D O I
10.1038/nm1364
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is a crucial need for alternatives to native vein or artery for vascular surgery. The clinical efficacy of synthetic, allogeneic or xenogeneic vessels has been limited by thrombosis, rejection, chronic inflammation and poor mechanical properties. Using adult human fibroblasts extracted from skin biopsies harvested from individuals with advanced cardiovascular disease, we constructed tissue-engineered blood vessels (TEBVs) that serve as arterial bypass grafts in long-term animal models. These TEBVs have mechanical properties similar to human blood vessels, without relying upon synthetic or exogenous scaffolding. The TEBVs are antithrombogenic and mechanically stable for 8 months in vivo. Histological analysis showed complete tissue integration and formation of vasa vasorum. The endothelium was confluent and positive for von Willebrand factor. A smooth muscle-specific alpha-actin-positive cell population developed within the TEBV, suggesting regeneration of a vascular media. Electron microscopy showed an endothelial basement membrane, elastogenesis and a complex collagen network. These results indicate that a completely biological and clinically relevant TEBV can be assembled exclusively from an individual's own cells.
引用
收藏
页码:361 / 365
页数:5
相关论文
共 26 条
[1]   A biological hybrid model for collagen-based tissue engineered vascular constructs [J].
Berglund, JD ;
Mohseni, MM ;
Nerem, RM ;
Sambanis, A .
BIOMATERIALS, 2003, 24 (07) :1241-1254
[2]   THE EVOLUTION OF MORPHOLOGICAL AND BIOMECHANICAL CHANGES IN REVERSED AND INSITU VEIN GRAFTS [J].
CAMBRIA, RP ;
MEGERMAN, J ;
BREWSTER, DC ;
HASSON, J ;
WARNOCK, DF ;
ABBOTT, WM .
ANNALS OF SURGERY, 1987, 205 (02) :167-174
[3]   Comparative reactivity and mechanical properties of human isolated internal mammary and radial arteries [J].
Chamiot-Clerc, P ;
Copie, X ;
Renaud, JF ;
Safar, M ;
Girerd, X .
CARDIOVASCULAR RESEARCH, 1998, 37 (03) :811-819
[4]   Dog peritoneal and pleural cavities as bioreactors to grow autologous vascular grafts [J].
Chue, WL ;
Campbell, GR ;
Caplice, N ;
Muhammed, A ;
Berry, CL ;
Thomas, AC ;
Bennett, MB ;
Campbell, JH .
JOURNAL OF VASCULAR SURGERY, 2004, 39 (04) :859-867
[5]   The role of inflammation in vascular injury and repair [J].
Davis, C ;
Fischer, J ;
Ley, K ;
Sarembock, IJ .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (08) :1699-1709
[6]   MECHANICAL-BEHAVIOR OF VASCULAR SMOOTH-MUSCLE IN CYLINDRICAL SEGMENTS OF ARTERIES INVITRO [J].
DOBRIN, PB .
ANNALS OF BIOMEDICAL ENGINEERING, 1984, 12 (05) :497-510
[7]  
GIRERD XJ, 1992, J HYPERTENS, V10, pS111
[8]  
Gittenberger-de Groot AC, 1999, ARTERIOSCL THROM VAS, V19, P1589
[9]  
Grenier G, 2003, IN VITRO CELL DEV-AN, V39, P131
[10]   Artificial blood vessel: The Holy Grail of peripheral vascular surgery [J].
Kakisis, JD ;
Liapis, CD ;
Breuer, C ;
Sumpio, BE .
JOURNAL OF VASCULAR SURGERY, 2005, 41 (02) :349-354