Suppr超能文献

抗体诱导的受体丧失。HepG2细胞中去唾液酸糖蛋白和去唾液酸糖蛋白受体的不同命运。

Antibody-induced receptor loss. Different fates for asialoglycoproteins and the asialoglycoprotein receptor in HepG2 cells.

作者信息

Schwartz A L, Ciechanover A, Merritt S, Turkewitz A

出版信息

J Biol Chem. 1986 Nov 15;261(32):15225-32.

PMID:3021767
Abstract

The human asialoglycoprotein receptor (ASGP-R) is a membrane glycoprotein which participates in receptor-mediated endocytosis and delivery of its ligands to lysosomes for degradation. In order to examine the pathways and mechanisms responsible for the turnover and degradation of the ASGP-R we have followed the fate of the ASGP-R in HepG2 cells during exposure to anti-receptor antibody as well as inhibitors of lysosomal processing and receptor recycling. Incubation of cells at 37 degrees C with anti-ASGP-R antibody results in the rapid (t 1/2 30 min) loss of mature 46,000-Da ASGP-R (control, t 1/2 20 h). This process requires whole IgG, since Fab fragments do not induce loss of receptor. Furthermore, this antibody-induced loss is specific, since incubation with antibody to the transferrin receptor does not alter cellular ASGP-R content. Of note, weak bases (e.g. primaquine) abrogate this antibody-induced loss of ASGP-R. Inhibitors of lysosomal proteases (EC64 and leupeptin) do not alter this antibody-mediated loss. Furthermore, this effect occurs at 18 degrees C, a temperature at which delivery of ligand to the lysosome is blocked. Thus, the present observations suggest a unique pathway for antibody-induced ASGP-R loss which is distinct from the pathway of lysosomal delivery of ligand.

摘要

人去唾液酸糖蛋白受体(ASGP-R)是一种膜糖蛋白,它参与受体介导的内吞作用,并将其配体递送至溶酶体进行降解。为了研究负责ASGP-R周转和降解的途径及机制,我们追踪了HepG2细胞中ASGP-R在暴露于抗受体抗体以及溶酶体加工和受体再循环抑制剂时的命运。在37℃下用抗ASGP-R抗体孵育细胞会导致成熟的46,000道尔顿ASGP-R迅速(半衰期30分钟)丢失(对照,半衰期20小时)。这个过程需要完整的IgG,因为Fab片段不会诱导受体丢失。此外,这种抗体诱导的丢失是特异性的,因为用抗转铁蛋白受体抗体孵育不会改变细胞ASGP-R的含量。值得注意的是,弱碱(如伯氨喹)可消除这种抗体诱导的ASGP-R丢失。溶酶体蛋白酶抑制剂(EC64和亮抑酶肽)不会改变这种抗体介导的丢失。此外,这种效应在18℃时出现,在该温度下配体向溶酶体的递送被阻断。因此,目前的观察结果提示了一种独特的抗体诱导ASGP-R丢失的途径,它不同于配体向溶酶体递送的途径。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验