New insights into fibrosis from the ECM degradation perspective: the macrophage-MMP-ECM interaction

Fibrosis is a pathological feature of a variety of chronic inflammatory diseases that can affect almost all organs, which can cause severe consequences and even lead to death. Fibrosis is characterized by the excessive accumulation of extracellular matrix (ECM) due to disruption of the balance between ECM production and degradation. Although overabundance of ECM proteins has long been the focus of studies on fibrosis, another facet of the problem-impaired degradation of the ECM-is gaining increasing attention. Matrix metalloproteinase (MMP) and the tissue inhibitor of metalloproteinase (TIMP) system is the main molecular system contributing to ECM degradation, and macrophages are the major regulators of ECM. However, the relationship among macrophages, the MMP/TIMP system and the ECM is not fully understood in the context of fibrosis. Here, we discuss in detail the role played by the ECM in the development of fibrosis and highlight the macrophage-MMP-ECM interaction that is involved in fibrogenesis and may be a potential therapeutic target for fibrosis.

Automated summary

Fibrosis is a pathological feature of various chronic inflammatory diseases, which can have severe consequences and even be fatal. The imbalance between the production and degradation of extracellular matrix (ECM) leads to excessive accumulation of ECM, with impaired degradation also playing a significant role in fibrosis. Understanding the relationship among macrophages, the MMP/TIMP system, and ECM is crucial for the development of potential therapeutic strategies for fibrosis.