Buddhist Tzu Chi Bioinnovation Center, Tzu Chi Foundation, Hualien 970, Taiwan.
Department of Medical Research, Hualien Tzu Chi Hospital, Hualien 970, Taiwan.
Molecules. 2019 Nov 19;24(22):4188. doi: 10.3390/molecules24224188.
Fibrosis is a type of chronic organ failure, resulting in the excessive secretion of extracellular matrix (ECM). ECM protects wound tissue from infection and additional injury, and is gradually degraded during wound healing. For some unknown reasons, myofibroblasts (the cells that secrete ECM) do not undergo apoptosis; this is associated with the continuous secretion of ECM and reduced ECM degradation even during de novo tissue formation. Thus, matrix metalloproteinases (MMPs) are considered to be a potential target of fibrosis treatment because they are the main groups of ECM-degrading enzymes. However, MMPs participate not only in ECM degradation but also in the development of various biological processes that show the potential to treat diseases such as stroke, cardiovascular diseases, and arthritis. Therefore, treatment involving the targeting of MMPs might impede typical functions. Here, we evaluated the links between these MMP functions and possible detrimental effects of fibrosis treatment, and also considered possible approaches for further applications.
纤维化是一种慢性器官衰竭,导致细胞外基质(ECM)的过度分泌。ECM 保护伤口组织免受感染和进一步损伤,并在伤口愈合过程中逐渐降解。由于某些未知原因,肌成纤维细胞(分泌 ECM 的细胞)不会发生细胞凋亡;这与 ECM 的持续分泌以及即使在新组织形成时 ECM 降解减少有关。因此,基质金属蛋白酶(MMPs)被认为是纤维化治疗的潜在靶点,因为它们是 ECM 降解酶的主要群体。然而,MMPs 不仅参与 ECM 的降解,还参与各种生物过程的发展,这些过程具有治疗中风、心血管疾病和关节炎等疾病的潜力。因此,针对 MMPs 的治疗可能会阻碍典型的功能。在这里,我们评估了这些 MMP 功能与纤维化治疗的潜在不利影响之间的联系,并考虑了进一步应用的可能方法。