1994
DOI: 10.1177/096368979400300505
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A New Technique for Isolating and Culturing Human Hepatocytes from Whole or Split Livers not Used for Transplantation

Abstract: Large numbers of human hepatocytes were obtained from split and whole livers by using an adaptive form of the collagenase perfusion technique employed in rodent and human biopsies. In order to guarantee a homogenous distribution of the perfusate within the whole specimen, major hepatic veins were cannulated with large bore catheters. This technique allowed for the isolation of human hepatocytes on a large scale (up to 18.5 x 10(9) in one case) from normal and diseased liver specimens. The yield of isolated nor… Show more

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Cited by 69 publications
(39 citation statements)
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“…Hepatocytes were isolated as previously described. 26 Confocal Laser Scanning Microscopy. Huh7 cells (5 ϫ10 4 ) or primary human hepatocytes were grown on cover slides in 24-well plates and incubated with 100 L purified wild-type or TLM nucleocapsids (20 nmol/L) isolated from triple-infected Sf9 cells that were diluted in DMEM.…”
Section: Methodsmentioning
confidence: 99%
“…Hepatocytes were isolated as previously described. 26 Confocal Laser Scanning Microscopy. Huh7 cells (5 ϫ10 4 ) or primary human hepatocytes were grown on cover slides in 24-well plates and incubated with 100 L purified wild-type or TLM nucleocapsids (20 nmol/L) isolated from triple-infected Sf9 cells that were diluted in DMEM.…”
Section: Methodsmentioning
confidence: 99%
“…In accordance with institutional guidelines, human hepatocytes were isolated from normal liver wedge resections by collagenase-P (Roche Diagnostics, Grenzau, Germany) digestion as recently described. 44,45 Briefly, after enzymatic digestion hepatocytes were separated from non-parenchymal cells by differential centrifugation at 50 g and then passed over a 30% Percoll (Pharmacia, Freiburg, FRG) gradient at a concentration of 10 6 cells/ml Percoll to obtain a highly purified cell population. Hepatocyte purity and viability assessed by microscopy was greater than 95% and viability consistently exceeded 90% by trypan blue exclusion.…”
Section: Cell Lines and Human Primary Hepatocytesmentioning
confidence: 99%
“…Hepatocyte purity and viability assessed by microscopy was greater than 95% and viability consistently exceeded 90% by trypan blue exclusion. 45 The primary hepatocytes were cultured in Williams Medium E, supplemented with 10% heatinactivated (90 min at 701C) FBS, 1% penicillin/streptomycin, 15 mM hepes buffer (all Life Technologies, Karlsruhe, FRG), 2.0 mg/ml insulin and 0.35 nM Hydrocortisone (both Sigma, Deisenhofen, FRG) at 371C, 5% CO 2 in a humidified atmosphere.…”
Section: Cell Lines and Human Primary Hepatocytesmentioning
confidence: 99%
“…11,49 In accordance with institutional guidelines, human hepatocytes were isolated from normal liver wedge resections by collagenase -P (Roche Diagnostics, Grenzau, Germany ) digestion as recently described. 50,51 Briefly, after enzymatic digestion hepatocytes were separated from nonparenchymal cells by differential centrifugation at 50Âg and then passed over a 30% Percoll (Pharmacia, Freiburg, Germany ) gradient at a concentration of 10 6 cells / mL Percoll to obtain a highly purified cell population. Hepatocyte purity and viability assessed by microscopy was greater than 95% and viability consistently exceeded 90% by trypan blue exclusion.…”
Section: Cell Lines and Cell Culturementioning
confidence: 99%
“…Hepatocyte purity and viability assessed by microscopy was greater than 95% and viability consistently exceeded 90% by trypan blue exclusion. 51 The primary hepatocytes were cultured in Williams Medium E, supplemented with 10% heat -inactivated (90 minutes at 708C ) FBS, 1% penicillin /streptomycin, 15 mM Hepes buffer (all Life Technologies, Karlsruhe, Germany ), 2.0 g /mL insulin, and 0.35 nM hydrocortisone ( both Sigma, Deisenhofen, Germnay ) at 378C, 5% CO 2 in a humidified atmosphere.…”
Section: Cell Lines and Cell Culturementioning
confidence: 99%