Type-1 Collagen differentially alters [beta]-catenin accumulation in primary Dupuytren's Disease cord and adjacent palmar fascia cells
Background Dupuytren's Disease (DD) is a debilitating contractile fibrosis of the palmar fascia characterised by excess collagen deposition, contractile myofibroblast development, increased Transforming Growth Factor-[beta] levels and [beta]-catenin accumulation. The aim of this study was to de...
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Veröffentlicht in: | BMC musculoskeletal disorders 2009-06, Vol.10, p.72 |
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Zusammenfassung: | Background Dupuytren's Disease (DD) is a debilitating contractile fibrosis of the palmar fascia characterised by excess collagen deposition, contractile myofibroblast development, increased Transforming Growth Factor-[beta] levels and [beta]-catenin accumulation. The aim of this study was to determine if a collagen-enriched environment, similar to in vivo conditions, altered [beta]-catenin accumulation by primary DD cells in the presence or absence of Transforming Growth Factor-[beta]. Methods Primary DD and patient matched, phenotypically normal palmar fascia (PF) cells were cultured in the presence or absence of type-1 collagen and Transforming Growth Factor-[beta]1. [beta]-catenin and [alpha]-smooth muscle actin levels were assessed by western immunoblotting and immunofluorescence microscopy. Results DD cells display a rapid depletion of cellular [beta]-catenin not evident in patient-matched PF cells. This effect was not evident in either cell type when cultured in the absence of type-1 collagen. Exogenous addition of Transforming Growth Factor-[beta]1 to DD cells in collagen culture negates the loss of [beta]-catenin accumulation. Transforming Growth Factor-[beta]1-induced [alpha]-smooth muscle actin, a marker of myofibroblast differentiation, is attenuated by the inclusion of type-1 collagen in cultures of DD and PF cells. Conclusion Our findings implicate type-1 collagen as a previously unrecognized regulator of [beta]-catenin accumulation and a modifier of TGF-[beta]1 signaling specifically in primary DD cells. These data have implications for current treatment modalities as well as the design of in vitro models for research into the molecular mechanisms of DD. |
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ISSN: | 1471-2474 1471-2474 |
DOI: | 10.1186/1471-2474-10-72 |