Effects of shear stress on metabolic function of the co-culture system of hepatocyte nonparenchymal cells for a bioartificial liver

被引:34
作者
Kan, P [1 ]
Miyoshi, H [1 ]
Yanagi, K [1 ]
Ohshima, N [1 ]
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba Sci City, Ibaraki 3058575, Japan
关键词
D O I
10.1097/00002480-199809000-00023
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
To improve the culture conditions of hepatocytes for use as a bioartificial liver, the effects of shear flow on the co-culture system of hepatocytes/nonparenchymal cells (NPC) were investigated. A flow chamber with a collagen coated rectangular glass plate, where hepatocytes (5 x 10(4) cell/cm(2)) and NPC (2 x 10(5) cell/cm(2)) were seeded, was used to attain a shear stress of 4.7 dyne/cm(2). Concentrations of ammonia and urea in the medium were measured daily during the 2 week experiment. The metabolic activity of hepatocytes in the homotypic culture were lower than those of the co-culture, especially when the cultivation time exceeded 1 week. In addition, the applied shear flow promoted activity of the co-culture system. An enhancement in the rates of ammonium removal and urea synthesis was obtained in the perfusion systems. Morphologic observation revealed that aggregates of hepatocytes formed abundantly in the perfusion system and hepatocytes developed a cuboid shape. This suggested that perfusion affected the function and morphology of hepatocytes in the co-culture system. Shear flow could induce cell-cell interactions and secretion of extracellular matrix through the activation of NPC.
引用
收藏
页码:M441 / M444
页数:4
相关论文
共 14 条
[1]   IMPROVED HEPATOCYTE IN-VITRO MAINTENANCE IN A CULTURE MODEL WITH WOVEN MULTICOMPARTMENT CAPILLARY SYSTEMS - ELECTRON-MICROSCOPY STUDIES [J].
GERLACH, JC ;
SCHNOY, N ;
ENCKE, J ;
SMITH, MD ;
MULLER, C ;
NEUHAUS, P .
HEPATOLOGY, 1995, 22 (02) :546-552
[2]   MAINTENANCE AND REVERSIBILITY OF ACTIVE ALBUMIN SECRETION BY ADULT-RAT HEPATOCYTES CO-CULTURED WITH ANOTHER LIVER EPITHELIAL-CELL TYPE [J].
GUGUENGUILLOUZO, C ;
CLEMENT, B ;
BAFFET, G ;
BEAUMONT, C ;
MORELCHANY, E ;
GLAISE, D ;
GUILLOUZO, A .
EXPERIMENTAL CELL RESEARCH, 1983, 143 (01) :47-54
[3]  
HAUSSINGER D, 1990, BIOCHEM J, V267, P281
[4]   New function of Ito cells in liver morphogenesis: Evidence using a novel morphogenic protein, epimorphin, in vitro [J].
Hirose, M ;
Watanabe, S ;
Oide, H ;
Kitamura, T ;
Miyazaki, A ;
Sato, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (01) :155-160
[5]  
KOBE HG, 1994, INT J ARTIF ORGANS, V17, P95
[6]   Strategies for restoration and maintenance of normal hepatic structure and function in long-term cultures of rat hepatocytes [J].
LeCluyse, EL ;
Bullock, PL ;
Parkinson, A .
ADVANCED DRUG DELIVERY REVIEWS, 1996, 22 (1-2) :133-186
[7]  
LOREAL O, 1993, AM J PATHOL, V143, P538
[8]  
Miyoshi H., 1994, Japanese Journal of Artificial Organs, V23, P479
[9]  
Ohshima N, 1997, ARTIF ORGANS, V21, P1169
[10]  
Powers MJ, 1997, BIOTECHNOL BIOENG, V53, P415, DOI 10.1002/(SICI)1097-0290(19970220)53:4<415::AID-BIT10>3.0.CO