The Diverse Pathways for Cell Surface MT1-MMP Localization in Migratory Cells

被引:1
作者
Kelly, Hannah [1 ]
Inada, Masaki [2 ,3 ]
Itoh, Yoshifumi [1 ,3 ]
机构
[1] Univ Oxford, Kennedy Inst Rheumatol, Nuffield Dept Orthopaed Rheumatol & Musculoskeleta, Oxford OX3 7FY, England
[2] Tokyo Univ Agr & Technol, Dept Biotechnol & Life Sci, 2-24-16 Nakacho, Koganei, Tokyo 1848588, Japan
[3] Tokyo Univ Agr & Technol, Inst Global Innovat Res, 2-24-16 Nakacho, Koganei, Tokyo 1848588, Japan
关键词
MT1-MMP; cell invasion; leading-edge; focal adhesion; invadopodia; TYPE-1; MATRIX-METALLOPROTEINASE; COLLAGEN-INDUCED ACTIVATION; GELATINASE-A MMP-2; INVADOPODIA FORMATION; TUMOR-GROWTH; SELECTIVE-INHIBITION; PROMMP-2; ACTIVATION; FIBRILLAR COLLAGEN; CYTOPLASMIC DOMAIN; IV COLLAGENASE;
D O I
10.3390/cells14030209
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Controlled cell migration is an essential biological process in health, while uncontrolled cell migration contributes to disease progression. For cells to migrate through tissue, they must first degrade the extracellular matrix (ECM), which acts as a physical barrier to cell migration. A type I transmembrane-type matrix metalloproteinase, MT1-MMP, is the key enzyme involved in this process. It has been extensively shown that MT1-MMP promotes the migration of different cell types in tissue, including fibroblasts, epithelial cells, endothelial cells, macrophages, mesenchymal stem cells, and cancer cells. MT1-MMP is tightly regulated at different levels, and its localization to leading-edge membrane structures is an essential process for MT1-MMP to promote cellular invasion. Different cells display different motility-associated membrane structures, which contribute to their invasive ability, and there are diverse mechanisms of MT1-MMP localization to these structures. In this article, we will discuss the current understanding of MT1-MMP regulation, in particular, localization mechanisms to these different motility-associated membrane structures.
引用
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页数:17
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