How Matrix Metalloproteinases Regulate Cell Behavior
Top Cited Papers
- 1 November 2001
- journal article
- review article
- Published by Annual Reviews in Annual Review of Cell and Developmental Biology
- Vol. 17 (1), 463-516
- https://doi.org/10.1146/annurev.cellbio.17.1.463
Abstract
▪ Abstract The matrix metalloproteinases (MMPs) constitute a multigene family of over 25 secreted and cell surface enzymes that process or degrade numerous pericellular substrates. Their targets include other proteinases, proteinase inhibitors, clotting factors, chemotactic molecules, latent growth factors, growth factor–binding proteins, cell surface receptors, cell-cell adhesion molecules, and virtually all structural extracellular matrix proteins. Thus MMPs are able to regulate many biologic processes and are closely regulated themselves. We review recent advances that help to explain how MMPs work, how they are controlled, and how they influence biologic behavior. These advances shed light on how the structure and function of the MMPs are related and on how their transcription, secretion, activation, inhibition, localization, and clearance are controlled. MMPs participate in numerous normal and abnormal processes, and there are new insights into the key substrates and mechanisms responsible for regula...Keywords
This publication has 226 references indexed in Scilit:
- Matrix Metalloproteinases Collagenase-2, Macrophage Elastase, Collagenase-3, and Membrane Type 1-Matrix Metalloproteinase Impair Clotting by Degradation of Fibrinogen and Factor XIIPublished by Elsevier ,2000
- Human Membrane Type-2 Matrix Metalloproteinase Is Defective in Cell-Associated Activation of Progelatinase ABiochemical and Biophysical Research Communications, 2000
- Expression and localization of macrophage elastase (matrix metalloproteinase-12) in abdominal aortic aneurysms.Journal of Clinical Investigation, 1998
- An Essential Role for Ectodomain Shedding in Mammalian DevelopmentScience, 1998
- High Affinity Binding of Latent Matrix Metalloproteinase-9 to the α2(IV) Chain of Collagen IVJournal of Biological Chemistry, 1998
- Identification of Insulin-like Growth Factor-binding Protein-1 as a Potential Physiological Substrate for Human Stromelysin-3Journal of Biological Chemistry, 1997
- Patterns and Emerging Mechanisms of the Angiogenic Switch during TumorigenesisCell, 1996
- T-Antigen inhibits metalloproteinase expression and invasion in human placental cells transformed with temperature-sensitive simian virus 40Matrix Biology, 1996
- Site-directed mutations that alter the inhibitory activity of the tissue inhibitor of metalloproteinases-1: importance of the N-terminal region between cysteine 3 and cysteine 13Biochemistry, 1992
- Collagenase production by human skin fibroblastsBiochemical and Biophysical Research Communications, 1975