Itoh Yoshifumi
Kennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
Front Cell Dev Biol. 2021 Nov 2;9:736735. doi: 10.3389/fcell.2021.736735. eCollection 2021.
Multicellular organisms are composed of cells and extracellular matrix (ECM). ECM is a network of multidomain macromolecules that fills gaps between cells. It acts as a glue to connect cells, provides scaffolding for migrating cells, and pools cytokines and growth factors. ECM also directly sends signals to the cells through ECM receptors, providing survival signals and migration cues. Altogether, ECM provides a correct microenvironment for the cells to function in the tissue. Although ECM acts as a signaling molecule, they are insoluble solid molecules, unlike soluble receptor ligands such as cytokines and growth factors. Upon cell binding to the ECM through ECM receptors and signals transmitted, cells then need to have a mechanism to release from ECM to prevent prolonged signals, which may be tumorigenic, and migrate on ECM. One effective means to release the cells from ECM is to cleave the ECM receptors by proteinases. In this mini-review, current knowledge of ECM receptor shedding will be discussed.
多细胞生物由细胞和细胞外基质(ECM)组成。ECM是一个多结构域大分子网络,填充细胞间的间隙。它起到连接细胞的胶水作用,为迁移细胞提供支架,并汇集细胞因子和生长因子。ECM还通过ECM受体直接向细胞发送信号,提供生存信号和迁移线索。总之,ECM为细胞在组织中发挥功能提供了正确的微环境。尽管ECM作为一种信号分子,但与细胞因子和生长因子等可溶性受体配体不同,它们是不溶性固体分子。细胞通过ECM受体与ECM结合并传递信号后,需要有一种机制从ECM中释放出来,以防止可能致癌的长时间信号,并在ECM上迁移。从ECM中释放细胞的一种有效方法是通过蛋白酶切割ECM受体。在这篇小型综述中,将讨论关于ECM受体脱落的当前知识。