High yield hepatocyte isolation from pig livers for investigation of hybrid liver support systems: Influence of collagenase concentration and body weight

被引:28
作者
Gerlach, J [1 ]
Brombacher, J [1 ]
Smith, M [1 ]
Neuhaus, P [1 ]
机构
[1] UNIV STRATHCLYDE,BIOENGN UNIT,GLASGOW,LANARK,SCOTLAND
关键词
D O I
10.1006/jsre.1996.0178
中图分类号
R61 [外科手术学];
学科分类号
摘要
Cultured hepatocytes would be required in large quantities if a hybrid liver support system became available, We have therefore performed a study of larger scale enzymatic hepatocyte isolation on whole pig livers, A new method of open-loop and recirculating perfusion in five steps using both the portal venous and the hepatic arterial vascular systems has been developed, In a study of the yield and cell viability of hepatocytes after isolation, the collagenase concentration of the perfusate was investigated over a range of 0.02 to 0.15%, The effect of animal weight on yield and cell viability was determined within the body weight range of 6 to 40 kg, At collagenase concentrations of less than 0.08%, yield and viability declined, As collagenase concentration increased, the yield continuously increased while the viability peaked at 0.1%, There was a decline of viability and yield with rising body weight, Optimal results were obtained with the lowest body weight (6 kg) which gave a yield of 95% (g wet weight) and a viability of 98% (trypan blue), This novel five-step collagenase perfusion technique with arterial perfusion appears to be reproducible and safe, Application of this method enables the large scale investigations to be undertaken towards the development of hybrid liver support. (C) 1996 Academic Press, Inc.
引用
收藏
页码:85 / 89
页数:5
相关论文
共 27 条
[1]  
Berry M N, 1974, Methods Enzymol, V32, P625
[2]   HIGH-YIELD PREPARATION OF ISOLATED RAT LIVER PARENCHYMAL CELLS - A BIOCHEMICAL AND FINE STRUCTURAL STUDY [J].
BERRY, MN ;
FRIEND, DS .
JOURNAL OF CELL BIOLOGY, 1969, 43 (03) :506-+
[3]   PROSPECTS FOR HEPATOCYTE TRANSPLANTATION [J].
BUMGARDNER, GL ;
FASOLA, C ;
SUTHERLAND, DER .
HEPATOLOGY, 1988, 8 (05) :1158-1161
[4]  
CAPERNA TJ, 1985, J ANIM SCI, V61, P1577
[5]  
GERLACH J, 1993, ARTIF ORGANS, V17, P950
[6]  
GERLACH JC, 1994, INT J ARTIF ORGANS, V17, P301
[7]   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
[8]   BIOREACTOR FOR A LARGER SCALE HEPATOCYTE IN-VITRO PERFUSION [J].
GERLACH, JC ;
ENCKE, J ;
HOLE, O ;
MULLER, C ;
RYAN, CJ ;
NEUHAUS, P .
TRANSPLANTATION, 1994, 58 (09) :984-988
[9]   NONENZYMATIC VERSUS ENZYMATIC HEPATOCYTE ISOLATION FROM PIG LIVERS FOR LARGER SCALE INVESTIGATIONS OF LIVER-CELL PERFUSION SYSTEMS [J].
GERLACH, JC ;
BROMBACHER, J ;
COURTNEY, JM ;
NEUHAUS, P .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1993, 16 (09) :677-681
[10]   COMPARISON OF 4 METHODS FOR MASS HEPATOCYTE ISOLATION FROM PIG AND HUMAN LIVERS [J].
GERLACH, JC ;
BROMBACHER, J ;
KLOPPEL, K ;
SCHNOY, N ;
NEUHAUS, P .
TRANSPLANTATION, 1994, 57 (09) :1318-1322