Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/67530
Title: Fibroblast viability and phenotypic changes within glycated stiffened three-dimensional collagen matrices
Author: Vicens-Zygmunt, V.
Estany, S.
Colom, Adai
Montes-Worboys, A.
Macahua, C.
Sanabria, A. J.
Llatjós, Roger
Escobar Campuzano, Ignacio
Manresa, Federico
Dorca i Sargatal, Jordi
Navajas Navarro, Daniel
Alcaraz Casademunt, Jordi
Molina-Molina, M.
Keywords: Fibroblasts
Col·lagen
Fibrosi pulmonar
Fibroblasts
Collagen
Pulmonary fibrosis
Issue Date: 1-Jul-2015
Publisher: BioMed Central
Abstract: Background: There is growing interest in the development of cell culture assays that enable the rigidity of the extracellular matrix to be increased. A promising approach is based on three-dimensional collagen type I matrices that are stiffened by cross-linking through non-enzymatic glycation with reducing sugars. Methods: The present study evaluated the biomechanical changes in the non-enzymatically glycated type I collagen matrices, including collagen organization, the advanced glycation end products formation and stiffness achievement. Gels were glycated with ribose at different concentrations (0, 5, 15, 30 and 240 mM). The viability and the phenotypic changes of primary human lung fibroblasts cultured within the non-enzymatically glycated gels were also evaluated along three consecutive weeks. Statistical tests used for data analyze were Mann<br>Whitney U, Kruskal Wallis, Student's t-test, two-way ANOVA, multivariate ANOVA, linear regression test and mixed linear model. Results: Our findings indicated that the process of collagen glycation increases the stiffness of the matrices and generates advanced glycation end products in a ribose concentration-dependent manner. Furthermore, we identified optimal ribose concentrations and media conditions for cell viability and growth within the glycated matrices. The microenvironment of this collagen based three-dimensional culture induces α-smooth muscle actin and tenascin-C fibroblast protein expression. Finally, a progressive contractile phenotype cell differentiation was associated with the contraction of these gels. Conclusions: The use of non-enzymatic glycation with a low ribose concentration may provide a suitable model with a mechanic and oxidative modified environment with cell s embedded in it, which allowed cell proliferation and induced fibroblast phenotypic changes. Such culture model could be appropriate for investigations of the behavior and phenotypic changes in cells that occur during lung fibrosis as well as for testing different antifibrotic therapies in vitro.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1186/s12931-015-0237-z
It is part of: Respiratory Research, 2015, vol. 16, p. 82-79
Related resource: http://dx.doi.org/10.1186/s12931-015-0237-z
URI: http://hdl.handle.net/2445/67530
ISSN: 1465-993X
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Fisiològiques)

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