Abstract
PURPOSE: To compare the viability of human hepatocytes dissociated by the ethylenediaminetetraacetic acid and collagenase techniques. METHODS: Hepatocytes were prepared by dissociation of liver fragments obtained from hepatectomies performed for therapeutic purposes at the Service of Digestive Tract Surgery, Federal University of Triângulo Mineiro. RESULTS: During the first 4 days of the experiment, 70% of the cells presented birefringent membranes and were not stained with 2% erythrosine, and were therefore considered to be viable. During the first 3 days, hepatocyte viability was on average 71% in the EDTA group and 76% in the collagenase group, with no significant difference between groups. No significant difference was observed between groups at any time. The secretion of albumin by the cultured hepatocytes was preserved up to the seventh day. Mean albumin secretion during the first 3 days was 50 µg/ml in the two groups and a reduction of albumin production was observed from the fourth to the seventh day. Again, no significant difference was observed between groups at any time. CONCLUSION: Cell viability and preservation of albumin secretion by hepatocytes are similar for the EDTA and collagenase techniques.
Reference16 articles.
1. Transplantation of highly differentiated immortalized human hepatocytes to treat acute liver failure;Kobayashi N;Transplantation,2000
2. Intrasplenic hepatocellular transplantation corrects hepatic encephalopathy in portacaval shunted rats;Ribeiro J;Hepatology,1992
3. Transplanted cryopreserved encapsuled porcine hepatocytes are as effective as fresh hepatocytes in preventinh death from cute failure in rats;Sarkis R;Transplantation,2000
4. Microencapsuled hepatocytes as a bioartificial liver;Sun AM;Trans. Am. Soc. Artif. Intern. Organs,1986
5. Transplantation of microcarriers-attached hepatocytes into 90% partially hepatectomized rats;Demetriou AA;Hepatology,1988