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对从正常大鼠肝脏分离出的不同细胞类型进行的亚细胞分级分离分析研究。

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

作者信息

Selden C, Wootton A M, Moss D W, Peters T J

出版信息

Clin Sci Mol Med. 1978 Nov;55(5):423-7. doi: 10.1042/cs0550423.

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.
摘要
  1. 通过用胶原酶溶液灌注从正常大鼠肝脏中分离出实质细胞、库普弗细胞和胆管细胞。2. 在分离的细胞匀浆中测定主要亚细胞器标记酶的比活性(酶活性单位/mg蛋白质),并与全肝匀浆进行比较。3. 将细胞破碎,提取物通过蔗糖密度梯度离心进行亚细胞分级分析。通过测定提取物中潜在的β-N-乙酰氨基葡萄糖苷酶来确定溶酶体的完整性。4. 在全肝、实质细胞和胆管细胞中,溶酶体、内质网和质膜标记酶的亚细胞分布相似。与其他组分相比,库普弗细胞中这些酶在胞质溶胶中的比例显著增加。此外,这些细胞中各种细胞器的平衡密度低于实质细胞中的平衡密度。

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