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肝脏中富含受体的细胞内膜囊泡运输去唾液酸转铁蛋白和胰岛素。

Receptor-rich intracellular membrane vesicles transporting asialotransferrin and insulin in liver.

作者信息

Debanne M T, Evans W H, Flint N, Regoeczi E

出版信息

Nature. 1982 Jul 22;298(5872):398-400. doi: 10.1038/298398a0.

Abstract

A wide range of receptors are located at the blood sinusoidal aspect of the hepatocyte plasma membrane. Many circulating ligands that bind to receptors on the cell surfaces are interiorized along two pathways. Asialoglycoproteins are transferred from the plasma membrane to lysosomes and degraded, whereas immunoglobulin A and bile acids are transported across the hepatocyte interior and released into bile. Asialotransferrin type 3 (ref. 6) follows a further pathway termed diacytosis. After binding to the asialoglycoprotein receptor, asialotransferrin is endocytosed and then returned to blood with a proportion of its carbohydrate side chains resialylated. We now describe in liver the properties of intracellular asialotransferrin-enclosing vesicles (diacytosomes) and show that they differ from Golgi, lysosome and plasma membrane fractions. Furthermore, we show that the asialoglycoprotein binding sites are located on the cytoplasmic (outer) surface of diacytosomes.

摘要

多种受体位于肝细胞质膜的血窦侧。许多与细胞表面受体结合的循环配体通过两条途径内化。去唾液酸糖蛋白从质膜转移至溶酶体并被降解,而免疫球蛋白A和胆汁酸则穿过肝细胞内部并释放到胆汁中。3型去唾液酸转铁蛋白(参考文献6)遵循另一条称为双胞吞作用的途径。与去唾液酸糖蛋白受体结合后,去唾液酸转铁蛋白被内吞,然后一部分碳水化合物侧链重新唾液酸化后返回血液。我们现在描述肝脏中包裹细胞内去唾液酸转铁蛋白的囊泡(双胞吞小体)的特性,并表明它们不同于高尔基体、溶酶体和质膜组分。此外,我们表明去唾液酸糖蛋白结合位点位于双胞吞小体的细胞质(外)表面。

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