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首页> 外文期刊>The Tohoku Journal of Experimental Medicine >Endocytosis in rat intrahepatic bile duct epithelial cells of horseradish peroxidase injected into the common bile duct or the portal vein.
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Endocytosis in rat intrahepatic bile duct epithelial cells of horseradish peroxidase injected into the common bile duct or the portal vein.

机译:辣根过氧化物酶在大鼠肝内胆管上皮细胞中的胞吞作用注入总胆管或门静脉。

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摘要

While recent data in intrahepatic bile duct epithelial cells (IBDECs) isolated from normal rat liver have established their ability to undergo endocytosis, few studies have assessed endocytosis in IBDECs in situ. Thus, to clarify the activity of IBDECs in situ on macro-molecules in bile and blood, we injected horseradish peroxidase (HRP) into either the common bile duct or the portal vein, and determined its intracellular distribution by electron microscopic cytochemistry. Successful retrograde injection into the common bile duct was achieved by resection of the liver surface so as to avoid HRP leakage from the bile duct on injection. IBDECs internalized HRP through both the apical and basolateral plasma membranes. By quantitative analysis, counting the number of HRP-positive vesicles in the cells, apical endocytosis was found more active than basolateral. HRP internalized through the apical membrane was either routed to the acid phosphatase-positive lysosomes for degradation or to extracellular space for transcytosis. HRP through the basolateral membrane was transferred to the organelles having lipid inclusion, which were expected to be lysosomes negative for acid phosphatase. Our results suggest that IBDECs in situ are actively engaged in endocytosis for degradation of macromolecules in bile and blood, and possibly engaged in the excretion of macromolecules into extracellular space.
机译:尽管从正常大鼠肝脏分离的肝内胆管上皮细胞(IBDECs)的最新数据已经确立了它们进行内吞作用的能力,但很少有研究评估IBDECs原位的内吞作用。因此,为了阐明IBDECs对胆汁和血液中大分子的原位活性,我们将辣根过氧化物酶(HRP)注入胆总管或门静脉,并通过电子显微镜细胞化学确定其在细胞内的分布。通过切除肝脏表面可成功逆行注入胆总管,从而避免HRP在注入时从胆管漏出。 IBDECs通过顶端和基底外侧质膜使HRP内在化。通过定量分析,计数细胞中HRP阳性囊泡的数量,发现顶端内吞作用比基底外侧更活跃。通过顶膜内化的HRP要么被送至酸性磷酸酶阳性溶酶体进行降解,要么被送至胞外空间进行转胞吞作用。 HRP通过基底外侧膜转移到具有脂质包裹体的细胞器中,这些细胞器预计是酸性磷酸酶阴性的溶酶体。我们的结果表明,原位IBDECs积极参与内吞作用,降解胆汁和血液中的大分子,并可能参与将大分子排泄到细胞外空间。

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