Matrix-Bound PAI-1 Supports Cell Blebbing via RhoA/ROCK1 Signaling
Author(s) -
Amandine Cartier-Michaud,
Michel Malo,
Cécile CharrièreBertrand,
Gilles Gadéa,
Christelle Anguille,
Ajitha Supiramaniam,
Annick Lesne,
Franck Delaplace,
Guillaume Hutzler,
Pierre Roux,
Daniel A. Lawrence,
Georgia BarlovatzMeimon
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0032204
Subject(s) - rock1 , rhoa , microbiology and biotechnology , tumor microenvironment , cancer research , biology , cell , cyr61 , extracellular matrix , cancer cell , cell migration , matricellular protein , metastasis , chemistry , signal transduction , cancer , receptor , growth factor , ctgf , biochemistry , genetics , tumor cells
The microenvironment of a tumor can influence both the morphology and the behavior of cancer cells which, in turn, can rapidly adapt to environmental changes. Increasing evidence points to the involvement of amoeboid cell migration and thus of cell blebbing in the metastatic process; however, the cues that promote amoeboid cell behavior in physiological and pathological conditions have not yet been clearly identified. Plasminogen Activator Inhibitor type-1 (PAI-1) is found in high amount in the microenvironment of aggressive tumors and is considered as an independent marker of bad prognosis. Here we show by immunoblotting, activity assay and immunofluorescence that, in SW620 human colorectal cancer cells, matrix-associated PAI-1 plays a role in the cell behavior needed for amoeboid migration by maintaining cell blebbing, localizing PDK1 and ROCK1 at the cell membrane and maintaining the RhoA/ROCK1/MLC-P pathway activation. The results obtained by modeling PAI-1 deposition around tumors indicate that matrix-bound PAI-1 is heterogeneously distributed at the tumor periphery and that, at certain spots, the elevated concentrations of matrix-bound PAI-1 needed for cancer cells to undergo the mesenchymal-amoeboid transition can be observed. Matrix-bound PAI-1, as a matricellular protein, could thus represent one of the physiopathological requirements to support metastatic formation.
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