Document Detail


ECM stiffness primes the TGFβ pathway to promote chondrocyte differentiation.
MedLine Citation:
PMID:  22833566     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Cells encounter physical cues such as extracellular matrix (ECM) stiffness in a microenvironment replete with biochemical cues. However, the mechanisms by which cells integrate physical and biochemical cues to guide cellular decision making are not well defined. Here we investigate mechanisms by which chondrocytes generate an integrated response to ECM stiffness and transforming growth factor β (TGFβ), a potent agonist of chondrocyte differentiation. Primary murine chondrocytes and ATDC5 cells grown on 0.5-MPa substrates deposit more proteoglycan and express more Sox9, Col2α1, and aggrecan mRNA relative to cells exposed to substrates of any other stiffness. The chondroinductive effect of this discrete stiffness, which falls within the range reported for articular cartilage, requires the stiffness-sensitive induction of TGFβ1. Smad3 phosphorylation, nuclear localization, and transcriptional activity are specifically increased in cells grown on 0.5-MPa substrates. ECM stiffness also primes cells for a synergistic response, such that the combination of ECM stiffness and exogenous TGFβ induces chondrocyte gene expression more robustly than either cue alone through a p38 mitogen-activated protein kinase-dependent mechanism. In this way, the ECM stiffness primes the TGFβ pathway to efficiently promote chondrocyte differentiation. This work reveals novel mechanisms by which cells integrate physical and biochemical cues to exert a coordinated response to their unique cellular microenvironment.
Authors:
Jessica L Allen; Margaret E Cooke; Tamara Alliston
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2012-07-25
Journal Detail:
Title:  Molecular biology of the cell     Volume:  23     ISSN:  1939-4586     ISO Abbreviation:  Mol. Biol. Cell     Publication Date:  2012 Sep 
Date Detail:
Created Date:  2012-09-17     Completed Date:  2013-03-04     Revised Date:  2013-04-01    
Medline Journal Info:
Nlm Unique ID:  9201390     Medline TA:  Mol Biol Cell     Country:  United States    
Other Details:
Languages:  eng     Pagination:  3731-42     Citation Subset:  IM    
Affiliation:
UC Berkeley-UCSF Graduate Program in Bioengineering, University of California, San Francisco, San Francisco, CA 94143, USA.
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MeSH Terms
Descriptor/Qualifier:
Aggrecans / genetics,  metabolism
Animals
Blotting, Western
Cell Differentiation / drug effects*
Cell Line
Cells, Cultured
Chondrocytes / cytology,  drug effects*,  metabolism
Collagen Type II / genetics,  metabolism
Extracellular Matrix / chemistry,  metabolism*
Gene Expression / drug effects
Mice
Phosphorylation / drug effects
Physical Phenomena
Reverse Transcriptase Polymerase Chain Reaction
SOX9 Transcription Factor / genetics,  metabolism
Signal Transduction
Smad3 Protein / metabolism
Transforming Growth Factor beta / genetics,  metabolism,  pharmacology*
rho-Associated Kinases / metabolism
Grant Support
ID/Acronym/Agency:
R01 DE019284/DE/NIDCR NIH HHS; R01DE019284/DE/NIDCR NIH HHS; //Howard Hughes Medical Institute
Chemical
Reg. No./Substance:
0/Aggrecans; 0/Col2a1 protein, mouse; 0/Collagen Type II; 0/SOX9 Transcription Factor; 0/Smad3 Protein; 0/Smad3 protein, mouse; 0/Sox9 protein, mouse; 0/Transforming Growth Factor beta; EC 2.7.11.1/rho-Associated Kinases
Comments/Corrections

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