MT1‐MMP: A potent modifier of pericellular microenvironment
Top Cited Papers
- 26 May 2005
- journal article
- review article
- Published by Wiley in Journal of Cellular Physiology
- Vol. 206 (1), 1-8
- https://doi.org/10.1002/jcp.20431
Abstract
Cells are regulated by many different means, and there is more and more evidence emerging that changes in the microenvironment greatly affect cell function. MT1‐MMP is a type I transmembrane proteinase which participates in pericellular proteolysis of extracellular matrix (ECM) macromolecules. The enzyme is cellular collagenase essential for skeletal development, cancer invasion, growth, and angiogenesis. MT1‐MMP promotes cell invasion and motility by pericellular ECM degradation, shedding of CD44 and syndecan1, and by activating ERK. Thus MT1‐MMP is one of the factors that influence the cellular microenvironment and thereby affect cell‐signaling pathways and eventually alters cellular behavior. As a proteinase, MT1‐MMP is regulated by inhibitors, but it also requires formation of a homo‐oligomer complex, localization to migration front of the cells, and internalization to become a “functionally active” cell function modifier. Developing new means to inhibit “functional activity” of MT1‐MMP may be a new direction to establish treatments for the diseases that MT1‐MMP mediates such as cancer and rheumatoid arthritis.Keywords
This publication has 86 references indexed in Scilit:
- Intracellular processing and activation of membrane type 1 matrix metalloprotease depends on its partitioning into lipid domainsJournal of Cell Science, 2004
- The syndecan-1 ectodomain regulates αvβ3 integrin activity in human mammary carcinoma cellsThe Journal of cell biology, 2004
- Mint-3 Regulates the Retrieval of the Internalized Membrane-type Matrix Metalloproteinase, MT5-MMP, to the Plasma Membrane by Binding to Its Carboxyl End Motif EWVJournal of Biological Chemistry, 2004
- Distinct Roles for the Catalytic and Hemopexin Domains of Membrane Type 1-Matrix Metalloproteinase in Substrate Degradation and Cell MigrationJournal of Biological Chemistry, 2004
- Glycosylation Broadens the Substrate Profile of Membrane Type 1 Matrix MetalloproteinaseJournal of Biological Chemistry, 2004
- Matrix metalloproteinases: a tail of a frog that became a princeNature Reviews Molecular Cell Biology, 2002
- Processing of Integrin αv Subunit by Membrane Type 1 Matrix Metalloproteinase Stimulates Migration of Breast Carcinoma Cells on Vitronectin and Enhances Tyrosine Phosphorylation of Focal Adhesion KinaseJournal of Biological Chemistry, 2002
- Functional Interplay between Type I Collagen and Cell Surface Matrix Metalloproteinase ActivityJournal of Biological Chemistry, 2001
- Activation of a recombinant membrane type 1‐matrix metalloproteinase (MT1‐MMP) by furin and its interaction with tissue inhibitor of metalloproteinases (TIMP)‐2FEBS Letters, 1996
- Tumor Cell Interactions with the Extracellular Matrix During Invasion and MetastasisAnnual Review of Cell Biology, 1993