紧密连接
并行传输
肝细胞
胆汁淤积
生物
信使核糖核酸
肝内胆管
内科学
阿尔法(金融)
胆管
内分泌学
分子生物学
细胞生物学
生物化学
基因
医学
磁导率
膜
护理部
体外
患者满意度
结构效度
作者
Michael B. Fallon,Albert Mennone,James M. Anderson
出处
期刊:American Journal of Physiology-cell Physiology
[American Physiological Society]
日期:1993-06-01
卷期号:264 (6): C1439-C1447
被引量:35
标识
DOI:10.1152/ajpcell.1993.264.6.c1439
摘要
Hepatocyte tight junctions form the intercellular barrier between bile and blood. Cholestasis due to common bile duct ligation (CBDL) results in structural changes in the tight junction (TJ) and an overt paracellular leak, although the molecular basis for these alterations is undefined. Using the epithelial isoform of the TJ protein ZO-1 (ZO-1 alpha +) as a marker for molecular changes in hepatocyte TJs, we investigated the effects of CBDL on ZO-1 alpha + immunofluorescence (IF) localization and on ZO-1 alpha + mRNA and protein expression over 2 wk of CBDL. ZO-1 alpha + IF staining was altered after 2 days of CBDL and appeared to accumulate in pericanalicular regions after 7 and 9 days. Quantitative immunoblotting and ribonuclease protection revealed a marked increase in hepatic ZO-1 alpha + protein expression and ZO-1 alpha + mRNA levels, respectively. In contrast to changes in ZO-1 alpha + IF, which occurred throughout the lobule, and changes in mRNA and protein expression, which were maximal after 9 days of ligation, the maximal hepatocyte proliferation occurred within 2 days after CBDL and was confined to periportal regions. CBDL results in altered hepatic localization and increased expression of the TJ protein ZO-1 alpha + and appears to represent a specific response by hepatocytes to pathological junction injury independent of cell proliferation.
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