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本文引用的文献

1
Tumor necrosis factor α-mediated cleavage and inactivation of SirT1 in human osteoarthritic chondrocytes.肿瘤坏死因子α介导人骨关节炎软骨细胞中SirT1的裂解和失活。
Arthritis Rheum. 2011 Aug;63(8):2363-73. doi: 10.1002/art.30279.
2
The design and synthesis of novel N-hydroxyformamide inhibitors of ADAM-TS4 for the treatment of osteoarthritis.新型 N-羟基甲酰胺 ADAM-TS4 抑制剂的设计与合成及其在骨关节炎治疗中的应用。
Bioorg Med Chem Lett. 2011 Mar 1;21(5):1376-81. doi: 10.1016/j.bmcl.2011.01.036. Epub 2011 Jan 18.
3
Proteinase-activated receptor-2 gene disruption limits the effect of osteoarthritis on cartilage in mice: a novel target in joint degradation.蛋白酶激活受体-2 基因敲除可减轻骨关节炎对小鼠软骨的影响:关节降解的新靶点。
J Rheumatol. 2011 May;38(5):911-20. doi: 10.3899/jrheum.100710. Epub 2011 Feb 1.
4
Association of ADAM12-S protein with radiographic features of knee osteoarthritis and bone and cartilage markers.ADAM12-S 蛋白与膝关节骨关节炎的影像学特征及骨和软骨标志物的相关性。
Rheumatol Int. 2012 Feb;32(2):519-23. doi: 10.1007/s00296-010-1717-6. Epub 2011 Jan 22.
5
Replication studies in various ethnic populations do not support the association of the HIF-2α SNP rs17039192 with knee osteoarthritis.在不同种族人群中的重复研究不支持缺氧诱导因子-2α单核苷酸多态性rs17039192与膝关节骨关节炎之间的关联。
Nat Med. 2011 Jan;17(1):26-7; author reply 27-9. doi: 10.1038/nm0111-26.
6
Structure-activity analysis of cathepsin K/chondroitin 4-sulfate interactions.组织蛋白酶 K/硫酸软骨素 4 相互作用的结构-活性分析。
J Biol Chem. 2011 Mar 18;286(11):8988-98. doi: 10.1074/jbc.M110.126706. Epub 2010 Dec 30.
7
Elevated aggrecanase activity in a rat model of joint injury is attenuated by an aggrecanase specific inhibitor.关节损伤大鼠模型中聚集蛋白水解酶活性升高可被聚集蛋白水解酶特异性抑制剂所抑制。
Osteoarthritis Cartilage. 2011 Mar;19(3):315-23. doi: 10.1016/j.joca.2010.12.004. Epub 2010 Dec 14.
8
Role of proinflammatory cytokines in the pathophysiology of osteoarthritis.促炎细胞因子在骨关节炎病理生理学中的作用。
Nat Rev Rheumatol. 2011 Jan;7(1):33-42. doi: 10.1038/nrrheum.2010.196. Epub 2010 Nov 30.
9
The role of the cartilage matrix in osteoarthritis.软骨基质在骨关节炎中的作用。
Nat Rev Rheumatol. 2011 Jan;7(1):50-6. doi: 10.1038/nrrheum.2010.198. Epub 2010 Nov 30.
10
Regulation of mechanical stress-induced MMP-13 and ADAMTS-5 expression by RUNX-2 transcriptional factor in SW1353 chondrocyte-like cells.RUNX-2 转录因子调控机械应力诱导的软骨细胞样细胞中 MMP-13 和 ADAMTS-5 的表达。
Osteoarthritis Cartilage. 2011 Feb;19(2):222-32. doi: 10.1016/j.joca.2010.11.004. Epub 2010 Nov 19.

参与骨关节炎软骨基质降解的蛋白酶。

Proteases involved in cartilage matrix degradation in osteoarthritis.

作者信息

Troeberg Linda, Nagase Hideaki

机构信息

The Kennedy Institute of Rheumatology Division, Imperial College London, London, UK.

出版信息

Biochim Biophys Acta. 2012 Jan;1824(1):133-45. doi: 10.1016/j.bbapap.2011.06.020. Epub 2011 Jul 8.

DOI:10.1016/j.bbapap.2011.06.020
PMID:21777704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3219800/
Abstract

Osteoarthritis is a common joint disease for which there are currently no disease-modifying drugs available. Degradation of the cartilage extracellular matrix is a central feature of the disease and is widely thought to be mediated by proteinases that degrade structural components of the matrix, primarily aggrecan and collagen. Studies on transgenic mice have confirmed the central role of Adamalysin with Thrombospondin Motifs 5 (ADAMTS-5) in aggrecan degradation, and the collagenolytic matrix metalloproteinase MMP-13 in collagen degradation. This review discusses recent advances in current understanding of the mechanisms regulating expression of these key enzymes, as well as reviewing the roles of other proteinases in cartilage destruction. This article is part of a Special Issue entitled: Proteolysis 50 years after the discovery of lysosome.

摘要

骨关节炎是一种常见的关节疾病,目前尚无改善病情的药物。软骨细胞外基质的降解是该疾病的核心特征,人们普遍认为这是由蛋白酶介导的,这些蛋白酶降解基质的结构成分,主要是聚集蛋白聚糖和胶原蛋白。对转基因小鼠的研究证实了含血小板反应蛋白基序的解聚素金属蛋白酶5(ADAMTS-5)在聚集蛋白聚糖降解中的核心作用,以及胶原酶基质金属蛋白酶MMP-13在胶原蛋白降解中的作用。本综述讨论了目前对这些关键酶表达调控机制的最新认识进展,并回顾了其他蛋白酶在软骨破坏中的作用。本文是名为:溶酶体发现50年后的蛋白水解的特刊的一部分。