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胆总管结扎诱导的肝外胆汁淤积期间大鼠肝细胞微丝与紧密连接之间结构相互作用紊乱。

Disturbed structural interactions between microfilaments and tight junctions in rat hepatocytes during extrahepatic cholestasis induced by common bile duct ligation.

作者信息

Song J Y, Van Marle J, Van Noorden C J, Frederiks W M

机构信息

Academic Medical Center, University of Amsterdam, The Netherlands.

出版信息

Histochem Cell Biol. 1996 Dec;106(6):573-80. doi: 10.1007/BF02473272.

Abstract

Microfilaments in epithelial cells are important for the structural and functional integrity of tight junctions. In the present study, we examined the relationship between microfilaments and tight junctions in hepatocytes of rat liver following common bile duct ligation (CBDL) for up to 2 weeks. Actin filaments and tight junctions were studied by fluorescence microscopy using 7-nitrobenzene-2-oxa-1,3-diazole phallacidin (NBD-ph) and an anti-ZO-1 antibody, respectively. Double-stained sections were examined with confocal laser scanning microscopy (CLSM). Electron microscopy was applied for the assessment of structural alterations in microfilaments and in tight junctions with detergent-extraction and freeze-fracture preparations. Our results showed that F-actin was present at the entire plasma membrane of hepatocytes in control liver, whereas CBDL increased the amount of F-actin mainly at the bile canalicular and lateral plasma membranes. Simultaneously, the immunofluorescence of ZO-1 underwent striking changes, i.e., from a uniform to an irregular staining pattern with various fluorescence intensities. CLSM demonstrated a colocalization of ZO-1 and F-actin in control liver and its deterioration in CBDL liver. Electron microscopy showed marked alterations of microfilaments and tight junctions due to CBDL. It is concluded that actin filaments are intimately associated with tight junctions in normal hepatocytes. CBDL impairs this association by progressively diminishing the structural interaction between F-actin and ZO-1, which may in turn lead to functional disturbances of tight junctions.

摘要

上皮细胞中的微丝对于紧密连接的结构和功能完整性至关重要。在本研究中,我们检测了大鼠肝脏肝细胞中微丝与紧密连接在胆总管结扎(CBDL)长达2周后的关系。分别使用7-硝基苯-2-恶唑-1,3-二氮杂萘鬼笔环肽(NBD-ph)和抗ZO-1抗体通过荧光显微镜研究肌动蛋白丝和紧密连接。用共聚焦激光扫描显微镜(CLSM)检查双重染色切片。应用电子显微镜通过去污剂提取和冷冻断裂制剂评估微丝和紧密连接的结构改变。我们的结果表明,在对照肝脏中,F-肌动蛋白存在于肝细胞的整个质膜上,而CBDL主要增加了胆小管和质膜外侧的F-肌动蛋白量。同时,ZO-1的免疫荧光发生了显著变化,即从均匀染色模式变为具有不同荧光强度的不规则染色模式。CLSM显示在对照肝脏中ZO-1和F-肌动蛋白共定位,而在CBDL肝脏中其共定位情况变差。电子显微镜显示由于CBDL,微丝和紧密连接有明显改变。结论是,肌动蛋白丝在正常肝细胞中与紧密连接密切相关。CBDL通过逐渐减少F-肌动蛋白和ZO-1之间的结构相互作用来损害这种关联,这反过来可能导致紧密连接的功能紊乱。

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