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MGP翻译后修饰及其抑制血管钙化分子机制的研究进展

洪敏雯 李清峰 刘康 梁丹 李世新 郝振宇

中国病理生理杂志2024,Vol.40Issue(12):2359-2366,8.
中国病理生理杂志2024,Vol.40Issue(12):2359-2366,8.DOI:10.3969/j.issn.1000-4718.2024.12.021

MGP翻译后修饰及其抑制血管钙化分子机制的研究进展

Progress in post-translational modification and molecular mechanism of MGP as a vascular calcification inhibitor

洪敏雯 1李清峰 2刘康 1梁丹 1李世新 1郝振宇1

作者信息

  • 1. 扬州大学生物科学与技术学院,江苏 扬州 225009
  • 2. 扬州大学附属医院,江苏 扬州 225009
  • 折叠

摘要

Abstract

The matrix gamma-carboxyglutamate protein(MGP),a vitamin K-dependent protein,inhibits arte-rial calcification.The substance's ability to inhibit calcification is linked to its post-translational modifications,specifical-ly γ-glutamyl carboxylation and phosphorylation.The molecular mechanism of the calcification inhibitor remains unclear due to its low solubility and complicated post-translational modifications.In this section,we summarize current research and ongoing debates about post-translational modifications of MGP and its mechanism for inhibiting calcification.We re-viewed recent research on diseases associated with MGP deficiency,such as cardiovascular disease,chronic kidney dis-ease,and Keutel syndrome.Hopefully,this review can help us understand how MGP functions as a vascular calcification inhibitor and identify potential treatments for diseases resulting from its dysfunction.

关键词

基质γ-羧基谷氨酸蛋白/翻译后修饰/钙化抑制

Key words

matrix gamma-carboxyglutamate protein/post-translational modification/calcification inhibition

分类

医药卫生

引用本文复制引用

洪敏雯,李清峰,刘康,梁丹,李世新,郝振宇..MGP翻译后修饰及其抑制血管钙化分子机制的研究进展[J].中国病理生理杂志,2024,40(12):2359-2366,8.

基金项目

国家自然科学基金资助项目(No.82370136) (No.82370136)

江苏省自然科学基金资助项目(No.BK20210828 ()

No.BK20231333) ()

江苏省特聘教授资助项目 ()

江苏省高等学校自然科学基金面上项目(No.21KJB610002) (No.21KJB610002)

中国博士后科学基金面上项目(No.2023M732983) (No.2023M732983)

中国病理生理杂志

OA北大核心CSTPCD

1000-4718

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