Analysis of multivariables during porcine liver digestion to improve hepatocyte yield and viability for use in bioartificial liver support systems
- PMID: 10972332
Analysis of multivariables during porcine liver digestion to improve hepatocyte yield and viability for use in bioartificial liver support systems
Abstract
In order to achieve optimal BALSS function, preparation of porcine hepatocytes with high yield, viability, and P450 activity is known to be important. To date hepatocyte yields have varied from 0.58 x 10(10) to 3.45 x 10(10) and viabilities from 75% to 95% within and between laboratories, even when using the same digestion methods and procedures, indicating that hepatocyte isolation during porcine liver digestion is not fully optimized. The aim of this work was to identify the critical parameters affecting cell recovery during porcine liver harvesting by investigating 21 variables involved in the process, including pig body and liver weight, different digestion times of perfusates, pH, a range of concentrations of sodium and chloride in EDTA, and collagenase perfusates. Univariate and multivariate analysis of a retrospective study (n = 23) revealed that low perfusate pH during the process of digestion had a positive effect on hepatocyte yield (p < 0.05), while high (relative) concentrations of sodium and chloride in the perfusates had significant negative effects on hepatocyte viability (both p < 0.05). Sodium and chloride had narrow optimal ranges for achieving a >90% viability. These findings were then tested in a prospective study (n = 10) and further verified. High hepatocyte viabilities (91.8+/-1.6% p = 0.036) and yields (2.56+/-0.48 x 10(10)) were achieved consistently, and P450IA1 activity was increased after sodium and chloride concentrations and pH in the perfusates were controlled. The physiological mechanism by which sodium and chloride affects hepatocyte viability during porcine liver digestion is discussed.
Similar articles
-
Analysis of Multivariables during Porcine Liver Digestion to Improve Hepatocyte Yield and Viability for Use in Bioartificial Liver Support Systems.Cell Transplant. 2000 May;9(3):329-336. doi: 10.1177/096368970000900304. Cell Transplant. 2000. PMID: 28880657
-
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
-
Isolation and cultivation of porcine hepatocytes for extracorporeal artificial liver support system.Chin Med J (Engl). 2001 Sep;114(9):946-9. Chin Med J (Engl). 2001. PMID: 11780388
-
[Development of a bioartificial liver using porcine hepatocyte spheroids].Nihon Rinsho. 1997 Sep;55(9):2451-7. Nihon Rinsho. 1997. PMID: 9301315 Review. Japanese.
-
Isolated hepatocytes--past, present and future.Cell Biol Toxicol. 1997 Jul;13(4-5):223-33. doi: 10.1023/a:1007402505482. Cell Biol Toxicol. 1997. PMID: 9298243 Review.
Cited by
-
Clinical translation of bioartificial liver support systems with human pluripotent stem cell-derived hepatic cells.World J Gastroenterol. 2017 Mar 21;23(11):1974-1979. doi: 10.3748/wjg.v23.i11.1974. World J Gastroenterol. 2017. PMID: 28373763 Free PMC article. Review.