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重组人CREG蛋白与溶酶体组织蛋白酶和M6P/IGFⅡR的相互作用

孙鸣宇 闫承慧 田孝祥 李洋 韩雅玲

中国组织工程研究Issue(37):5961-5965,5.
中国组织工程研究Issue(37):5961-5965,5.DOI:10.3969/j.issn.2095-4344.2015.37.011

重组人CREG蛋白与溶酶体组织蛋白酶和M6P/IGFⅡR的相互作用

Interactions between the recombinant human CREG protein and cathepsins and M6P/IGFIIR

孙鸣宇 1闫承慧 1田孝祥 1李洋 1韩雅玲1

作者信息

  • 1. 解放军沈阳军区总医院全军心血管病研究所心内科,辽宁省沈阳市 110016
  • 折叠

摘要

Abstract

BACKGROUND:It has been found that cel ular repressor of E1A-stimulated genes (CREG) is a lysosomal protein binding directly to the mannose-6-phosphate (M6P)/insulin-like growth factor II receptor (IGFIIR) and depends on the interaction with M6P receptors for efficient delivery to lysosomes OBJECTIVE:To study the interactions between the exogenous CREG protein and cathepsins and M6P/IGFIIR and to confirm the effect of CREG protein on expression and distribution of M6P/IGFIIR. METHODS:Double-stained immunofluorescence and coimmunoprecipitation were applied to observe the interactions between the exogenous CREG protein and cathepsin B, cathepsin L and M6P/IGFIIR. Using gain-of-function and loss-of-function approaches, the effect of CREG on expression and distribution of M6P/IGFIIR were studied by western blot assay and immunofluorescence staining. RESULTS AND CONCLUSION:Double-stained immunofluorescence and coimmunoprecipitation analyses confirmed the direct interactions between the exogenous CREG protein and cathepsin B, cathepsin L and M6P/IGFIIR. It was verified that CREG plays a critical role not in the expression but in the distribution of M6P/IGFIIR using gain-of-function and loss-of-function approaches. These findings provide evidence that exogenous CREG protein is located in lysosomes and has interactions with cathepsins and M6P/IGFIIR, also CREG plays a critical role in the distribution of M6P/IGFIIR.

关键词

组织构建/组织工程/巨噬细胞/E1A激活基因阻遏子/溶酶体/动脉粥样硬化/国家自然科学基金

分类

医药卫生

引用本文复制引用

孙鸣宇,闫承慧,田孝祥,李洋,韩雅玲..重组人CREG蛋白与溶酶体组织蛋白酶和M6P/IGFⅡR的相互作用[J].中国组织工程研究,2015,(37):5961-5965,5.

基金项目

国家自然科学基金资助项目(81130072,81370243) (81130072,81370243)

中国组织工程研究

OA北大核心CSTPCD

2095-4344

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