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佛波酯诱导细胞表面肝素结合表皮生长因子样生长因子的快速加工:从旁分泌生长因子活性转变为自分泌生长因子活性。

Phorbol ester induces the rapid processing of cell surface heparin-binding EGF-like growth factor: conversion from juxtacrine to paracrine growth factor activity.

作者信息

Goishi K, Higashiyama S, Klagsbrun M, Nakano N, Umata T, Ishikawa M, Mekada E, Taniguchi N

机构信息

Department of Biochemistry, Osaka University Medical School, Japan.

出版信息

Mol Biol Cell. 1995 Aug;6(8):967-80. doi: 10.1091/mbc.6.8.967.

Abstract

Vero cell heparin-binding epidermal growth factor-like growth factor (HB-EGF) is synthesized as a 20- to 30-kDa membrane-anchored HB-EGF precursor (proHB-EGF). Localization and processing of proHB-EGF, both constitutive and 12-O-tetradecanoylphorbol 13-acetate (TPA)-inducible, was examined in Vero cells overexpressing recombinant HB-EGF (Vero H cells). Flow cytometry and fluorescence immunostaining demonstrated that Vero cell proHB-EGF is cell surface-associated and localized at the interface of cell to cell contact. Cell surface biotinylation and immunoprecipitation detected a 20- to 30-kDa heterogeneous proHB-EGF species. Vero H cell surface proHB-EGF turned over constitutively with a half-life of 1.5 h. Some of the 20- to 30-kDa cell surface-associated proHB-EGF was processed and a 14-kDa species of bioactive HB-EGF was released slowly, but most of the proHB-EGF was internalized, displaying a diffuse immunofluorescent staining pattern and accumulation of proHB-EGF in endosomes. Addition of TPA induced a rapid processing of proHB-EGF at a Pro148-Val149 site with a half-life of 7min. The TPA effect was abrogated by the protein kinase C inhibitors, staurosporine and H7. Kinetic analysis showed that loss of cell surface proHB-EGF is maximal at 30 min after addition of TPA and that proHB-EGF is resynthesized and the initial cell surface levels are regained within 12-24 h. Loss of cell surface proHB-EGF was concomitant with appearance of 14- and 19-kDa soluble HB-EGF species in conditioned medium. Vero H cell-associated proHB-EGF is a juxtacrine growth factor for EP170.7 cells in coculture. Processing of proHB-EGF resulted in loss of juxtacrine activity and a simultaneous increase in soluble HB-EGF paracrine mitogenic activity. It was concluded that processing regulates HB-EGF bioactivity by converting it from a cell-surface juxtacrine growth factor to a processed, released soluble paracrine growth factor.

摘要

非洲绿猴肾细胞(Vero细胞)的肝素结合表皮生长因子样生长因子(HB-EGF)以20至30 kDa的膜锚定HB-EGF前体(proHB-EGF)形式合成。在过表达重组HB-EGF的Vero细胞(Vero H细胞)中,研究了组成型和12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导型proHB-EGF的定位和加工过程。流式细胞术和荧光免疫染色表明,Vero细胞proHB-EGF与细胞表面相关,定位于细胞间接触的界面处。细胞表面生物素化和免疫沉淀检测到一种20至30 kDa的异质性proHB-EGF种类。Vero H细胞表面的proHB-EGF以1.5小时的半衰期持续周转。一些20至30 kDa与细胞表面相关的proHB-EGF被加工,一种14 kDa的生物活性HB-EGF缓慢释放,但大部分proHB-EGF被内化,呈现弥漫性免疫荧光染色模式且proHB-EGF在内体中积累。添加TPA会诱导proHB-EGF在Pro148-Val149位点快速加工,半衰期为7分钟。蛋白激酶C抑制剂星形孢菌素和H7可消除TPA的作用。动力学分析表明,添加TPA后30分钟,细胞表面proHB-EGF的损失最大,且proHB-EGF会重新合成,初始细胞表面水平在12至24小时内恢复。细胞表面proHB-EGF的损失与条件培养基中14 kDa和19 kDa可溶性HB-EGF种类的出现同时发生。共培养时,Vero H细胞相关的proHB-EGF是EP170.7细胞的旁分泌生长因子。proHB-EGF的加工导致旁分泌活性丧失,同时可溶性HB-EGF旁分泌促有丝分裂活性增加。得出的结论是,加工通过将HB-EGF从细胞表面旁分泌生长因子转化为加工后释放的可溶性旁分泌生长因子来调节其生物活性。

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