» Articles » PMID: 22389410

Regulation of Invadopodia Formation and Activity by CD147

Overview
Journal J Cell Sci
Specialty Cell Biology
Date 2012 Mar 6
PMID 22389410
Citations 32
Authors
Affiliations
Soon will be listed here.
Abstract

A defining feature of malignant tumor progression is cellular penetration through the basement membrane and interstitial matrices that separate various cellular compartments. Accumulating evidence supports the notion that invasive cells employ specialized structures termed invadopodia to breach these structural barriers. Invadopodia are actin-based, lipid-raft-enriched membrane protrusions containing membrane-type-1 matrix metalloproteinase (MT1-MMP; also known as matrix metalloproteinase 14; MMP14) and several signaling proteins. CD147 (emmprin, basigin), an immunoglobulin superfamily protein that is associated with tumor invasion and metastasis, induces the synthesis of various matrix metalloproteinases in many systems. In this study we show that upregulation of CD147 is sufficient to induce MT1-MMP expression, invasiveness and formation of invadopodia-like structures in non-transformed, non-invasive, breast epithelial cells. We also demonstrate that CD147 and MT1-MMP are in close proximity within these invadopodia-like structures and co-fractionate in membrane compartments with the properties of lipid rafts. Moreover, manipulation of CD147 levels in invasive breast carcinoma cells causes corresponding changes in MT1-MMP expression, invasiveness and invadopodia formation and activity. These findings indicate that CD147 regulates invadopodia formation and activity, probably through assembly of MT1-MMP-containing complexes within lipid-raft domains of the invadopodia.

Citing Articles

Quantitative Membrane Proteomics for Discovery of Actionable Drug Targets at the Surface of RAS-Driven Human Cancer Cells.

Ye X Methods Mol Biol. 2024; 2823:27-46.

PMID: 39052212 DOI: 10.1007/978-1-0716-3922-1_3.


MCT4 and CD147 colocalize with MMP14 in invadopodia and support matrix degradation and invasion by breast cancer cells.

Meng S, Sorensen E, Ponniah M, Thorlacius-Ussing J, Crouigneau R, Larsen T J Cell Sci. 2024; 137(8).

PMID: 38661040 PMC: 11112124. DOI: 10.1242/jcs.261608.


Convergent Evolution Dynamics of SARS-CoV-2 and HIV Surface Envelope Glycoproteins Driven by Host Cell Surface Receptors and Lipid Rafts: Lessons for the Future.

Fantini J, Chahinian H, Yahi N Int J Mol Sci. 2023; 24(3).

PMID: 36768244 PMC: 9915253. DOI: 10.3390/ijms24031923.


Role of MMP-2 and CD147 in kidney fibrosis.

Cheng Z, Zhang X, Zhang Y, Li L, Chen P Open Life Sci. 2022; 17(1):1182-1190.

PMID: 36185410 PMC: 9482425. DOI: 10.1515/biol-2022-0482.


Matrix Metalloproteinases and Their Inhibitors in Pulmonary Fibrosis: EMMPRIN/CD147 Comes into Play.

Chulia-Peris L, Carreres-Rey C, Gabasa M, Alcaraz J, Carretero J, Pereda J Int J Mol Sci. 2022; 23(13).

PMID: 35805895 PMC: 9267107. DOI: 10.3390/ijms23136894.


References
1.
Nabeshima K, Iwasaki H, Koga K, Hojo H, Suzumiya J, Kikuchi M . Emmprin (basigin/CD147): matrix metalloproteinase modulator and multifunctional cell recognition molecule that plays a critical role in cancer progression. Pathol Int. 2006; 56(7):359-67. DOI: 10.1111/j.1440-1827.2006.01972.x. View

2.
Reddy V, Prabhu S, Mummidi S, Valente A, Venkatesan B, Shanmugam P . Interleukin-18 induces EMMPRIN expression in primary cardiomyocytes via JNK/Sp1 signaling and MMP-9 in part via EMMPRIN and through AP-1 and NF-kappaB activation. Am J Physiol Heart Circ Physiol. 2010; 299(4):H1242-54. PMC: 2957343. DOI: 10.1152/ajpheart.00451.2010. View

3.
Artym V, Yamada K, Mueller S . ECM degradation assays for analyzing local cell invasion. Methods Mol Biol. 2009; 522:211-9. DOI: 10.1007/978-1-59745-413-1_15. View

4.
Hu J, Mukhopadhyay A, Truesdell P, Chander H, Mukhopadhyay U, Mak A . Cdc42-interacting protein 4 is a Src substrate that regulates invadopodia and invasiveness of breast tumors by promoting MT1-MMP endocytosis. J Cell Sci. 2011; 124(Pt 10):1739-51. DOI: 10.1242/jcs.078014. View

5.
Ghatak S, Misra S, Toole B . Hyaluronan constitutively regulates ErbB2 phosphorylation and signaling complex formation in carcinoma cells. J Biol Chem. 2005; 280(10):8875-83. DOI: 10.1074/jbc.M410882200. View