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• W2046682016 abstract "1. Suspensions of rat liver cells were prepared by perfusing the liver in vitro with solutions containing collagenase and hyaluronidase. About 90% of the liver mass was recovered in the cell suspension. 2. Parenchymal cells were prepared by differential centrifugation or by magnetic removal of iron-loaded Kupffer cells. About 60% of the liver mass was regained in the parenchymal fractions. Specific activity of β glucoronidase (EC 3.2.1.31) was about the same in the parenchymal cells and in liver homogenates. Specific activity of acid deoxyribonuclease (EC 3.1.4.6) in parenchymal cells was about 65% of that in liver homogenates. 3. Kupffer cells were separated from parenchymal cells either by incubating the original cell suspension with pronase, which destroys the parenchymal cells, or by magnetic means. 70 and 40% of the Kupffer cells in the original cell suspension could be recovered by the pronase method and the magnet method, respectively. Iron-loaded cells were contaminated with parenchymal cells. Acid deoxyribonuclease and β-glucuronidase were found to be selectively concentrated in Kupffer cells prepared with pronase. Specific activities of β-glucuronidase and acid deoxyribonuclease were, respectively, 3.6 and 13.6 times higher in pronase-prepared Kupffer cells than in parenchymal cells. Only acid deoxyribonuclease was found to be increased in Kupffer cells isolated by means of a magnet (about twice as high as in parenchymal cells)." @default.
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• W2046682016 date "1973-10-01" @default.
• W2046682016 modified "2023-10-16" @default.
• W2046682016 title "Distribution of lysosomal enzymes between parenchymal and Kupffer cells of rat liver" @default.
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• W2046682016 doi "https://doi.org/10.1016/0005-2744(73)90201-5" @default.
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