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基质金属蛋白酶13在软骨重塑和关节炎中的研究进展

范凯健 吴菁 李钦 王婷玉

中国药理学通报2018,Vol.34Issue(5):607-611,5.
中国药理学通报2018,Vol.34Issue(5):607-611,5.DOI:10.3969/j.issn.1001-1978.2018.05.005

基质金属蛋白酶13在软骨重塑和关节炎中的研究进展

Advances in matrix metalloproteinase 13 in cartilage remodeling and arthritis

范凯健 1吴菁 2李钦 1王婷玉1

作者信息

  • 1. 上海交通大学医学院附属第九人民医院药剂科,上海 200011
  • 2. 上海市宝山区中西医结合医院药剂科,上海 201901
  • 折叠

摘要

Abstract

Arthritis is a common chronic disease characterized by the destruction of joint cartilage and inflammation in the sur-rounding tissues. Although it is known that the pathogenesis of arthritis is influenced by a series of factors, the underlying mechanisms remain unclarified. Recently, increasing attention has been paid to the increase of matrix metalloproteinases (MMPs) in articular cartilage,resulting in an inevitable degra-dation of cartilage and extracellular matrix (ECM). MMP-13, the major functioning enzyme during arthritis development,plays a vital role in the cartilage destruction, thus contributing to the decomposition of type Ⅱ collagen irreversibly. A variety of cellu-lar cytokines such as IL-1β and TNF-α,and Runx2 are assumed to affect the expression of MMP-13 in chondrocytes. The hypom-ethylation of the promoter region of the MMP-13 may induce its expression, while it can be reduced by inhibiting histone acety-lation. Meanwhile, microRNA can reduce the expression of MMP-13. In conclusion, MMP-13 can be used as an important therapeutic target in arthritis. In this review, we focus on the role of MMP-13 in arthritis and its underlying regulatory mecha-nisms.

关键词

关节炎/基质金属蛋白酶13/Ⅱ型胶原/Runx2/分子靶标/表观调控

Key words

arthritis/MMP-13/type Ⅱ collagen/Runx2/mo-lecular target/epigenetic

分类

医药卫生

引用本文复制引用

范凯健,吴菁,李钦,王婷玉..基质金属蛋白酶13在软骨重塑和关节炎中的研究进展[J].中国药理学通报,2018,34(5):607-611,5.

基金项目

国家自然科学基金资助项目(No 81301531,81572104) (No 81301531,81572104)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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