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胰岛素样生长因子I和II刺激内吞作用,但不影响人类成纤维细胞中溶酶体酶的分选。

Insulin-like growth factors I and II stimulate endocytosis but do not affect sorting of lysosomal enzymes in human fibroblasts.

作者信息

Braulke T, Tippmer S, Chao H J, von Figura K

机构信息

University of Göttingen, Biochemie II, Federal Republic of Germany.

出版信息

J Biol Chem. 1990 Apr 25;265(12):6650-5.

PMID:1969863
Abstract

The mannose 6-phosphate (Man-6-P)/insulin-like growth factor (IGF) II receptor has separate binding sites for Man-6-P and IGF II. It targets newly synthesized lysosomal enzymes from the Golgi to acidic pre-lysosomal organelles and mediates endocytosis of Man-6-P-containing ligands and IGF II. The two classes of ligands, Man-6-P and IGF II, as well as IGF I and the epidermal growth factor, induce in fibroblasts a transient redistribution of the receptor from internal membranes to the cell surface (Braulke, T., Tippmer, S., Neher, E., and von Figura, K. (1989) EMBO J. 8, 681-686). Here we show that the redistribution induced by IGF I and IGF II is accomplished without affecting the internalization rate of cell surface receptors. The redistribution results in an increased binding of ligands to the Man-6-P- and IGF II-binding sites of the receptor. Furthermore, the uptake of the lysosomal enzyme arylsulfatase A and of a Man-6-P neoglycoprotein is stimulated 2-3-fold by IGF I and IGF II, and this effect persists for at least 6 h. The IGF I- and IGF II-induced receptor redistribution does not affect the targeting of newly synthesized lysosomal enzymes. These results show that important functions of the Man-6-P/IGF II receptor such as binding and internalization of ligands can be up-regulated by the ligands of this receptor and other growth factors such as IGF I through redistribution of the receptor.

摘要

甘露糖6-磷酸(Man-6-P)/胰岛素样生长因子(IGF)II受体具有Man-6-P和IGF II的独立结合位点。它将来自高尔基体新合成的溶酶体酶靶向酸性前溶酶体细胞器,并介导含Man-6-P配体和IGF II的内吞作用。两类配体,即Man-6-P和IGF II,以及IGF I和表皮生长因子,可诱导成纤维细胞中该受体从内膜向细胞表面的短暂重新分布(布劳尔克,T.,蒂普默,S.,内尔,E.,和冯·菲古拉,K.(1989年)《欧洲分子生物学组织杂志》8,681 - 686)。在此我们表明,IGF I和IGF II诱导的重新分布是在不影响细胞表面受体内化速率的情况下完成的。这种重新分布导致配体与受体的Man-6-P和IGF II结合位点的结合增加。此外,IGF I和IGF II可使溶酶体酶芳基硫酸酯酶A和一种Man-6-P新糖蛋白的摄取增加2 - 3倍,且这种效应至少持续6小时。IGF I和IGF II诱导的受体重新分布不影响新合成溶酶体酶的靶向作用。这些结果表明,Man-6-P/IGF II受体的重要功能,如配体的结合和内吞作用,可通过该受体的配体以及其他生长因子如IGF I对受体的重新分布而上调。

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