基质金属蛋白酶
细胞外基质
下调和上调
椎间盘
细胞生物学
变性(医学)
发病机制
医学
分解代谢
MMP2型
生物信息学
癌症研究
生物
病理
解剖
内科学
生物化学
基因
新陈代谢
作者
Xiaosong Zou,Xingmin Zhang,Song Han,Lin Wei,Zhi Zheng,Yongjie Wang,Jingguo Xin,Shaokun Zhang
出处
期刊:Biochimie
[Elsevier BV]
日期:2023-05-31
卷期号:214: 27-48
被引量:13
标识
DOI:10.1016/j.biochi.2023.05.015
摘要
Intervertebral disc (IVD) degeneration (IDD) is a common disorder that affects the spine and is a major cause of lower back pain (LBP). The extracellular matrix (ECM) is the structural foundation of the biomechanical properties of IVD, and its degradation is the main pathological characteristic of IDD. Matrix metalloproteinases (MMPs) are a group of endopeptidases that play an important role in the degradation and remodeling of the ECM. Several recent studies have shown that the expression and activity of many MMP subgroups are significantly upregulated in degenerated IVD tissue. This upregulation of MMPs results in an imbalance of ECM anabolism and catabolism, leading to the degradation of the ECM and the development of IDD. Therefore, the regulation of MMP expression is a potential therapeutic target for the treatment of IDD. Recent research has focused on identifying the mechanisms by which MMPs cause ECM degradation and promote IDD, as well as on developing therapies that target MMPs. In summary, MMP dysregulation is a crucial factor in the development of IDD, and a deeper understanding of the mechanisms involved is needed to develop effective biological therapies that target MMPs to treat IDD.
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