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大鼠肝细胞表面膜的功能极性。从肝细胞血窦面、胆小管面及相邻表面分离和鉴定质膜亚组分。

Functional polarity of the rat hepatocyte surface membrane. Isolation and characterization of plasma-membrane subfractions from the blood-sinusoidal, bile-Canalicular and contiguous surfaces of the hepatocyte.

作者信息

Wisher M H, Evans W H

出版信息

Biochem J. 1975 Feb;146(2):375-88. doi: 10.1042/bj1460375.

DOI:10.1042/bj1460375
PMID:125584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1165315/
Abstract
  1. Six rat liver plasma-membrane subfractions of different density and morphological, enzymic and chemical properties were prepared from homogenates by a combination of differential, rate-zonal and density-gradient centrifugation. They consisted of three vesicular 'light' subfractions of density 1.12-1.13 and three 'heavy' subfractions of density 1.16-1.18 containing membrane strips and intercellular junctions. 2. All six subfractions contained a basal adenylate cyclase activity. One of the 'light' subfractions that showed the highest glucagon-stimulated adenylate cyclase activity was identified as deriving form the blood-sinusoidal face of the hepatocyte. This subfraction, unlike the others, was contaminated by Golgi components, as indicated by its morphological properties and the presence of galactosyl- and sialyl-transferase activities. 3. All the six subfractions showed high activities of the following plasma-membrane marker enzymes: 5'-nucleotidase, alkaline phosphodiesterase (nucleotide pyrophosphatase), alkaline phosphatase, leucine naphthylamidase and Mg2+-activated adenosine triphosphatase. A 'light' subfraction that showed the highest specific activities of all the above marker enzymes, but lacked a glucagon-stimulated adenylate cyclase activity, was identified as deriving from the bile-canalicular face of the hepatocyte. 4. The 'heavy' subfractions, which showed generally the lowest activities of the above plasma-membrane enzyme markers, and were characterized by the presence of desmosomes and gap junctions, were taken to originate from the contiguous faces of the hepatocyte. 5. The protein composition of the six subfractions was generally similar, as shown by polyacrylamide-gel electrophoresis. Differences in the amounts of various protein and glycoprotein bands among the subfractions correlated with their morphology, enzymic composition and sialic acid content. 6. Hormonal and histochemical evidence supporting the identification of a bile-canalicular subfraction, a blood-sinusoidal subfraction and contiguous-face subfractions is discussed.
摘要
  1. 通过差速离心、速率区带离心和密度梯度离心相结合的方法,从匀浆中制备出六种具有不同密度以及形态、酶学和化学性质的大鼠肝血浆膜亚组分。它们包括三种密度为1.12 - 1.13的囊泡状“轻”亚组分和三种密度为1.16 - 1.18的“重”亚组分,后者含有膜条带和细胞间连接。2. 所有六种亚组分都具有基础腺苷酸环化酶活性。其中一种“轻”亚组分表现出最高的胰高血糖素刺激的腺苷酸环化酶活性,被确定源自肝细胞的血窦面。与其他亚组分不同,该亚组分被高尔基体成分污染,这从其形态学性质以及半乳糖基转移酶和唾液酸转移酶活性的存在可以看出。3. 所有六种亚组分都表现出以下血浆膜标记酶的高活性:5'-核苷酸酶、碱性磷酸二酯酶(核苷酸焦磷酸酶)、碱性磷酸酶、亮氨酸萘基酰胺酶和Mg2+激活的腺苷三磷酸酶。一种在上述所有标记酶中表现出最高比活性但缺乏胰高血糖素刺激的腺苷酸环化酶活性的“轻”亚组分,被确定源自肝细胞的胆小管面。4. “重”亚组分通常表现出上述血浆膜酶标记的最低活性,其特征是存在桥粒和缝隙连接,被认为源自肝细胞的相邻面。5. 如聚丙烯酰胺凝胶电泳所示,六种亚组分的蛋白质组成总体相似。亚组分之间各种蛋白质和糖蛋白条带数量的差异与其形态、酶学组成和唾液酸含量相关。6. 讨论了支持鉴定胆小管亚组分、血窦亚组分和相邻面亚组分的激素和组织化学证据。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ca6/1165315/2e44a434fec3/biochemj00563-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ca6/1165315/3ea067e90969/biochemj00563-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ca6/1165315/2e44a434fec3/biochemj00563-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ca6/1165315/3ea067e90969/biochemj00563-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ca6/1165315/2e44a434fec3/biochemj00563-0102-a.jpg

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Functional polarity of the rat hepatocyte surface membrane. Isolation and characterization of plasma-membrane subfractions from the blood-sinusoidal, bile-Canalicular and contiguous surfaces of the hepatocyte.大鼠肝细胞表面膜的功能极性。从肝细胞血窦面、胆小管面及相邻表面分离和鉴定质膜亚组分。
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Improvement in the histochemical localization of leucine aminopeptidase with a new substrate, L-leucyl-4-methoxy-2-naphthylamide.使用新底物L-亮氨酰-4-甲氧基-2-萘酰胺改进亮氨酸氨基肽酶的组织化学定位。
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New insights into the pathogenesis of copper toxicosis in Wilson's disease: evidence for copper incorporation and defective canalicular transport of caeruloplasmin.威尔逊病中铜中毒发病机制的新见解:铜掺入及铜蓝蛋白胆小管转运缺陷的证据
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