Analytical subcellular fractionation studies on different cell types isolated from normal rat liver.

C Selden, A M Wootton, D W Moss, T J Peters
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引用次数: 12

Abstract

1. Parenchymal, Kupffer and biliary tract cells were isolated from normal rat liver by perfusion with collagenase solution. 2. The specific activities (munits of enzyme activity/mg of protein) of marker enzymes for the principal subcellular organelles were determined in the isolated cell homogenates and compared with whole liver homogenates. 3. The cells were disrupted and the extracts subjected to analytical subcellular fractionation by sucrose-density-gradient centrifugation. Lysosomal integrity was determined by assaying latent beta-N-acetylglucosaminidase in the extracts. 4. Similar subcellular distributions were found for lysosomal, endoplasmic reticulum and plasma membrane marker enzymes in the whole liver and in parenchymal and biliary tract cells. In Kupffer cells, the proportion of these enzymes in the cytosol was significantly increased compared with the other fractions. In addition the equilibrium densities of the various organelles in these cells were lower than those from parenchymal cells.

正常大鼠肝脏不同类型细胞的分析亚细胞分离研究。
1. 用胶原酶溶液灌注法分离正常大鼠肝脏实质细胞、库夫氏细胞和胆道细胞。2. 在分离的细胞匀浆中测定了主要亚细胞器的标记酶的比活性(酶活性单位/毫克蛋白质),并与全肝匀浆进行了比较。3.细胞被破坏,提取液通过蔗糖-密度梯度离心进行分析亚细胞分离。通过测定提取物中潜在的β - n -乙酰氨基葡萄糖酶测定溶酶体的完整性。4. 溶酶体、内质网和质膜标记酶在全肝、实质细胞和胆道细胞中的亚细胞分布相似。在Kupffer细胞中,与其他组分相比,这些酶在细胞质中的比例显著增加。此外,这些细胞中各种细胞器的平衡密度低于实质细胞。
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