Engineering liver therapies for the future

被引:72
作者
Allen, JW
Bhatia, SN
机构
[1] Univ Calif San Diego, Dept Bioengn, Microscale Tissue Engn Lab, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
来源
TISSUE ENGINEERING | 2002年 / 8卷 / 05期
关键词
D O I
10.1089/10763270260424097
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Treatment of liver disease has been greatly improved by the advent and evolution of liver transplantation. However, as demand for donor organs continues to increase beyond their availability, the need for alternative liver therapies is clear. Several approaches including extracorporeal devices, cell transplantation, and tissue-engineered constructs have been proposed as potential adjuncts or even replacements for transplantation. Simultaneously, experience from the liver biology community have provided valuable insight into tissue morphogenesis and in vitro stabilization of the hepatocyte phenotype. The next generation of cellular therapies must therefore consider incorporating cell sources and cellular microenvironments that provide both a large population of cells and strategies to maintain liver-specific functions over extended time frames. As cell-based therapies evolve, their success will require contribution from many diverse disciplines including regenerative medicine, developmental biology, and transplant medicine.
引用
收藏
页码:725 / 737
页数:13
相关论文
共 145 条
[21]   Bioencapsulated hepatocytes for experimental liver support [J].
Chang, TMS .
JOURNAL OF HEPATOLOGY, 2001, 34 (01) :148-149
[22]   Cerebral herniation in patients with acute liver failure is correlated with arterial ammonia concentration [J].
Clemmesen, JO ;
Larsen, FS ;
Kondrup, J ;
Hansen, BA ;
Ott, P .
HEPATOLOGY, 1999, 29 (03) :648-653
[23]   Expression of the human α1,2-fucosyltransferase in transgenic pigs modifies the cell surface carbohydrate phenotype and confers resistance to human serum-mediated cytolysis [J].
Costa, C ;
Zhao, L ;
Burton, WV ;
Bondioli, KR ;
Williams, BL ;
Hoagland, TA ;
Ditullio, PA ;
Ebert, KM ;
Fodor, WL .
FASEB JOURNAL, 1999, 13 (13) :1762-1773
[24]   TRANSPLANTATION OF MICROCARRIER-ATTACHED HEPATOCYTES INTO 90-PERCENT PARTIALLY HEPATECTOMIZED RATS [J].
DEMETRIOU, AA ;
REISNER, A ;
SANCHEZ, J ;
LEVENSON, SM ;
MOSCIONI, AD ;
CHOWDHURY, JR .
HEPATOLOGY, 1988, 8 (05) :1006-1009
[25]   NEW METHOD OF HEPATOCYTE TRANSPLANTATION AND EXTRACORPOREAL LIVER SUPPORT [J].
DEMETRIOU, AA ;
WHITING, J ;
LEVENSON, SM ;
CHOWDHURY, NR ;
SCHECHNER, R ;
MICHALSKI, S ;
FELDMAN, D ;
CHOWDHURY, JR .
ANNALS OF SURGERY, 1986, 204 (03) :259-271
[26]   SURVIVAL, ORGANIZATION, AND FUNCTION OF MICROCARRIER-ATTACHED HEPATOCYTES TRANSPLANTED IN RATS [J].
DEMETRIOU, AA ;
LEVENSON, SM ;
NOVIKOFF, PM ;
NOVIKOFF, AB ;
CHOWDHURY, NR ;
WHITING, J ;
REISNER, A ;
CHOWDHURY, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (19) :7475-7479
[27]  
Demetriou AA, 1997, ANN SURG, V225, P493
[28]   THERAPEUTIC EFFICACY OF THE TRANSPLANTATION OF ISOLATED HEPATOCYTES IN RATS WITH SURGICALLY INDUCED ACUTE HEPATIC-FAILURE - A STUDY OF THE MECHANISM [J].
DEMMA, I ;
HOUSSIN, D ;
CAPRON, M ;
MINATO, M ;
MORIN, J ;
GIGOU, M ;
SZEKELY, AM ;
BISMUTH, H .
EUROPEAN SURGICAL RESEARCH, 1986, 18 (01) :12-18
[29]   LONG-TERM CULTURE OF HEPATOCYTES - EFFECT OF HORMONES ON ENZYME-ACTIVITIES AND METABOLIC CAPACITY [J].
DICH, J ;
VIND, C ;
GRUNNET, N .
HEPATOLOGY, 1988, 8 (01) :39-45
[30]  
DIXIT V, 1992, ARTIF ORGANS, V16, P336