Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA USA.
Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA USA.
Matrix Biol. 2015 May-Jul;44-46:113-21. doi: 10.1016/j.matbio.2015.03.002. Epub 2015 Mar 11.
Repair following injury involves a range of processes - such as re-epithelialization, scar formation, angiogenesis, inflammation, and more - that function, often together, to restore tissue architecture. MMPs carry out diverse roles in all of these activities. In this article, we discuss how specific MMPs act on ECM during two critical repair processes: re-epithelialization and resolution of scar tissue. For wound closure, we discuss how two MMPs - MMP1 in human epidermis and MMP7 in mucosal epithelia - facilitate re-epithelialization by cleaving different ECM or ECM-associated proteins to affect similar integrin:matrix adhesion. In scars and fibrotic tissues, we discuss that a variety of MMPs carry out a diverse range of activities that can either promote or limit ECM deposition. However, few of these MMP-driven activities have been demonstrated to be due a direct action on ECM.
修复以下损伤涉及一系列过程 - 如再上皮化、瘢痕形成、血管生成、炎症等 - 这些过程通常共同作用以恢复组织结构。MMP 在所有这些活动中都具有多种功能。在本文中,我们讨论了特定的 MMP 在两个关键修复过程中如何作用于 ECM:再上皮化和瘢痕组织的解决。对于伤口闭合,我们讨论了两种 MMP - 人类表皮中的 MMP1 和粘膜上皮中的 MMP7 - 如何通过切割不同的 ECM 或 ECM 相关蛋白来影响类似的整合素:基质粘附,从而促进再上皮化。在疤痕和纤维化组织中,我们讨论了多种 MMP 进行了各种活动,这些活动既可以促进也可以限制 ECM 的沉积。然而,很少有这些 MMP 驱动的活动被证明是由于对 ECM 的直接作用。