α -1抗胰蛋白酶(AAT)及其在PiMZ表型个体肝脏中的刺激作用。“招聘-秘书阻碍”(R-SB)现象。

Liver Pub Date : 1984-10-01
F Callea, J Fevery, G Massi, C Lievens, J de Groote, V J Desmet
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引用次数: 0

摘要

临床刺激条件下的PiMZ个体显示肝脏α -1-抗胰蛋白酶(AAT)的特殊免疫组织化学染色模式:1)阳性涉及大区域实质(高达100%的肝细胞);2) 2区和3区肝细胞呈月牙形或沿窦状曲线呈直线排列。这种新的模式被称为II型,与I型相反,I型发生在门静脉周围肝细胞,以包涵体的形式遍布整个细胞质。这种特殊的染色模式与血清AAT升高有关,被认为是肝脏反应性的表达。II型阳性标志着新招募的肝细胞用于合成AAT;由于其输出缺陷,zaat保留在细胞内并通过免疫组织化学检测到。因此,这种染色模式是合成募集和分泌阻滞的表达(“募集-分泌阻滞”“R-SB”现象)。在PiMZ个体中,分泌阻滞选择性地、专一地影响AAT的Z部分。在电镜水平上,绝大多数保留的蛋白质在内质网中发现,内质网代表了主要和最早的储存部位。从目前糖蛋白生物合成的知识框架来看,本研究的结果进一步揭示了Z AAT缺陷的性质和细胞部位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alpha-1-antitrypsin (AAT) and its stimulation in the liver of PiMZ phenotype individuals. A "recruitment-secretory block" ("R-SB") phenomenon.

PiMZ individuals in conditions of clinical stimulation show a peculiar immunohistochemical staining pattern for alpha-1-antitrypsin (AAT) in the liver: 1) the positivity involves large zones of parenchyma (up to 100% of hepatocytes); 2) in zone 2 and zone 3 hepatocytes the positivity appears in the form of crescents or rectilinear arrays along the sinusoids. This new pattern is designated type II, in contrast to type I which occurs in periportal hepatocytes in the form of inclusions spread over the whole cytoplasm. This peculiar staining pattern is associated with serum elevation of AAT and is considered to be an expression of liver reactivity. Type II positivity marks the hepatocytes which are newly recruited for the synthesis of AAT; owing to its defective export, the Z AAT is retained within the cell and detectable by immunohistochemistry. Thus this staining pattern is an expression of both recruitment for synthesis and block of secretion ("Recruitment-Secretory Block" "R-SB" phenomenon). In PiMZ individuals, the secretory block affects selectively and exclusively the Z fraction of AAT. At the EM level the vast majority of the retained protein is found in the RER, which represents the major and the earliest site of storage. Viewed in the framework of present knowledge of glycoprotein biosynthesis, the results of this study shed further light on the nature and cellular site of the Z AAT defect.

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