Comparison of four methods for mass hepatocyte isolation from pig and human livers
- PMID: 8184468
- DOI: 10.1097/00007890-199405150-00005
Comparison of four methods for mass hepatocyte isolation from pig and human livers
Abstract
Using the pig liver, parameters for large scale hepatocyte isolation were studied in order to develop a technique suitable for human organs. These investigations led to a 5-step modification of the original 2-step method. Four groups were compared. A nonenzymatic EDTA perfusion technique has been shown to be inconvenient for mass cell isolation. The enzymatic 2-step perfusion, using 0.08% collagenase and 20-kg pigs, resulted in a mean hepatocyte viability of 61 +/- 1.9%, with a mean yield of 67 +/- 6.5% wet weight of the organ. The enzymatic 5-step method resulted in a mean hepatocyte viability of 74 +/- 1.7% with a mean yield of 80 +/- 1.8% wet weight. Five-step portal venous perfusion in combination with arterial perfusion resulted in 76 +/- 2.6% viability with a yield of 82 +/- 6.1%. The results were dependent on collagenase concentration and weight of the donors, improving with decreasing body weight. The 5-step method with combined arterial and portal vein perfusion developed for pig liver was used for mass human liver cell isolation with a minimum viability of 57% and a minimum yield of 58% wet weight.
Similar articles
-
Nonenzymatic versus enzymatic hepatocyte isolation from pig livers for larger scale investigations of liver cell perfusion systems.Int J Artif Organs. 1993 Sep;16(9):677-81. Int J Artif Organs. 1993. PMID: 8294161
-
High yield hepatocyte isolation from pig livers for investigation of hybrid liver support systems: influence of collagenase concentration and body weight.J Surg Res. 1996 Apr;62(1):85-9. doi: 10.1006/jsre.1996.0178. J Surg Res. 1996. PMID: 8606516
-
Comparison of pig hepatocyte isolation using intraoperative perfusion without warm ischemia and isolation of cells from abattoir organs after warm ischemia.Artif Organs. 1993 Nov;17(11):950-3. doi: 10.1111/j.1525-1594.1993.tb00409.x. Artif Organs. 1993. PMID: 8110065
-
[Cell culture and its application primary culture of human hepatocytes and its application].Gan To Kagaku Ryoho. 1992 Aug;19(9):1411-9. Gan To Kagaku Ryoho. 1992. PMID: 1503493 Review. Japanese.
-
Hepatocyte suspensions and cultures as tools in experimental carcinogenesis.J Toxicol Environ Health. 1979 Mar-May;5(2-3):551-60. doi: 10.1080/15287397909529766. J Toxicol Environ Health. 1979. PMID: 224209 Review.
Cited by
-
Dynamics of amino acid metabolism of primary human liver cells in 3D bioreactors.Bioprocess Biosyst Eng. 2006 Apr;28(5):331-40. doi: 10.1007/s00449-005-0040-1. Epub 2006 Mar 21. Bioprocess Biosyst Eng. 2006. PMID: 16550345 Free PMC article.
-
Experimental hepatocyte xenotransplantation--a comprehensive review of the literature.Xenotransplantation. 2015 Jul-Aug;22(4):239-48. doi: 10.1111/xen.12170. Epub 2015 May 7. Xenotransplantation. 2015. PMID: 25950141 Free PMC article. Review.
-
Recent advances in 2D and 3D in vitro systems using primary hepatocytes, alternative hepatocyte sources and non-parenchymal liver cells and their use in investigating mechanisms of hepatotoxicity, cell signaling and ADME.Arch Toxicol. 2013 Aug;87(8):1315-530. doi: 10.1007/s00204-013-1078-5. Epub 2013 Aug 23. Arch Toxicol. 2013. PMID: 23974980 Free PMC article. Review.
-
Transplantation of hepatocytes from genetically engineered pigs into baboons.Xenotransplantation. 2017 Mar;24(2):10.1111/xen.12289. doi: 10.1111/xen.12289. Epub 2017 Jan 28. Xenotransplantation. 2017. PMID: 28130881 Free PMC article.
-
Concept for modular extracorporeal liver support for the treatment of acute hepatic failure.Metab Brain Dis. 2002 Dec;17(4):477-84. doi: 10.1023/a:1021938708670. Metab Brain Dis. 2002. PMID: 12602523 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources