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hrs结合蛋白在RBL-2H3肥大细胞中IgE受体触发的胞吐作用中的参与。

Involvement of hrs binding protein in IgE receptor-triggered exocytosis in RBL-2H3 mast cells.

作者信息

Murai S, Kitamura N

机构信息

Department of Biological Sciences, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan.

出版信息

Biochem Biophys Res Commun. 2000 Nov 2;277(3):752-6. doi: 10.1006/bbrc.2000.3749.

Abstract

Hrs binding protein (Hbp) tightly associated with Hrs is thought to play a regulatory role in vesicular trafficking during endocytosis and exocytosis. In this study, we have expressed dominant-negative mutants of Hbp to evaluate their effects on the degranulation of secretory granules in RBL-2H3 mast cells. The dominant-negative mutants of Hbp significantly inhibited IgE receptor (FcepsilonRI)-triggered secretory response as tested by beta-hexosaminidase release. These results suggest that Hbp functions as a regulator in the FcepsilonRI-triggered degranulation of secretory granules in mast cells.

摘要

与Hrs紧密相关的Hrs结合蛋白(Hbp)被认为在胞吞作用和胞吐作用期间的囊泡运输中发挥调节作用。在本研究中,我们表达了Hbp的显性负性突变体,以评估它们对RBL-2H3肥大细胞中分泌颗粒脱颗粒的影响。如通过β-己糖胺酶释放所检测的,Hbp的显性负性突变体显著抑制了IgE受体(FcepsilonRI)触发的分泌反应。这些结果表明,Hbp在肥大细胞中FcepsilonRI触发的分泌颗粒脱颗粒过程中起调节作用。

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