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Reversible and irreversible differentiation of cardiac fibroblasts

AIMS: Differentiation of cardiac fibroblasts (Fbs) into myofibroblasts (MyoFbs) is responsible for connective tissue build-up in myocardial remodelling. We examined MyoFb differentiation and reversibility. METHODS AND RESULTS: Adult rat cardiac Fbs were cultured on a plastic substratum providing mec...

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Autores principales: Driesen, Ronald B., Nagaraju, Chandan K., Abi-Char, Joëlle, Coenen, Tamara, Lijnen, Paul J., Fagard, Robert H., Sipido, Karin R., Petrov, Victor V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928002/
https://www.ncbi.nlm.nih.gov/pubmed/24368833
http://dx.doi.org/10.1093/cvr/cvt338
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author Driesen, Ronald B.
Nagaraju, Chandan K.
Abi-Char, Joëlle
Coenen, Tamara
Lijnen, Paul J.
Fagard, Robert H.
Sipido, Karin R.
Petrov, Victor V.
author_facet Driesen, Ronald B.
Nagaraju, Chandan K.
Abi-Char, Joëlle
Coenen, Tamara
Lijnen, Paul J.
Fagard, Robert H.
Sipido, Karin R.
Petrov, Victor V.
author_sort Driesen, Ronald B.
collection PubMed
description AIMS: Differentiation of cardiac fibroblasts (Fbs) into myofibroblasts (MyoFbs) is responsible for connective tissue build-up in myocardial remodelling. We examined MyoFb differentiation and reversibility. METHODS AND RESULTS: Adult rat cardiac Fbs were cultured on a plastic substratum providing mechanical stress, with conditions to obtain different levels of Fb differentiation. Fb spontaneously differentiated to proliferating MyoFb (p-MyoFb) with stress fibre formation decorated with alpha-smooth muscle actin (α-SMA). Transforming growth factor-β1 (TGF-β1) promoted differentiation into α-SMA-positive MyoFb showing near the absence of proliferation, i.e. non-p-MyoFb. SD-208, a TGF-β-receptor-I (TGF-β-RI) kinase blocker, inhibited p-MyoFb differentiation as shown by stress fibre absence, low α-SMA expression, and high proliferation levels. Fb seeded in collagen matrices induced no contraction, whereas p-MyoFb and non-p-MyoFb induced 2.5- and four-fold contraction. Fb produced little collagen but high levels of interleukin-10. Non-p-MyoFb had high collagen production and high monocyte chemoattractant protein-1 and tissue inhibitor of metalloproteinases-1 levels. Transcriptome analysis indicated differential activation of gene networks related to differentiation of MyoFb (e.g. paxilin and PAK) and reduced proliferation of non-p-MyoFb (e.g. cyclins and cell cycle regulation). Dedifferentiation of p-MyoFb with stress fibre de-polymerization, but not of non-p-MyoFb, was induced by SD-208 despite maintained stress. Stress fibre de-polymerization could also be induced by mechanical strain release in p-MyoFb and non-p-MyoFb (2-day cultures in unrestrained 3-D collagen matrices). Only p-MyoFb showed true dedifferentiation after long-term 3-D cultures. CONCLUSIONS: Fb, p-MyoFb, and non-p-MyoFb have a distinct gene expression, ultrastructural, and functional profile. Both reduction in mechanical strain and TGF-β-RI kinase inhibition can reverse p-MyoFb differentiation but not non-p-MyoFb.
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spelling pubmed-39280022014-03-12 Reversible and irreversible differentiation of cardiac fibroblasts Driesen, Ronald B. Nagaraju, Chandan K. Abi-Char, Joëlle Coenen, Tamara Lijnen, Paul J. Fagard, Robert H. Sipido, Karin R. Petrov, Victor V. Cardiovasc Res Original Articles AIMS: Differentiation of cardiac fibroblasts (Fbs) into myofibroblasts (MyoFbs) is responsible for connective tissue build-up in myocardial remodelling. We examined MyoFb differentiation and reversibility. METHODS AND RESULTS: Adult rat cardiac Fbs were cultured on a plastic substratum providing mechanical stress, with conditions to obtain different levels of Fb differentiation. Fb spontaneously differentiated to proliferating MyoFb (p-MyoFb) with stress fibre formation decorated with alpha-smooth muscle actin (α-SMA). Transforming growth factor-β1 (TGF-β1) promoted differentiation into α-SMA-positive MyoFb showing near the absence of proliferation, i.e. non-p-MyoFb. SD-208, a TGF-β-receptor-I (TGF-β-RI) kinase blocker, inhibited p-MyoFb differentiation as shown by stress fibre absence, low α-SMA expression, and high proliferation levels. Fb seeded in collagen matrices induced no contraction, whereas p-MyoFb and non-p-MyoFb induced 2.5- and four-fold contraction. Fb produced little collagen but high levels of interleukin-10. Non-p-MyoFb had high collagen production and high monocyte chemoattractant protein-1 and tissue inhibitor of metalloproteinases-1 levels. Transcriptome analysis indicated differential activation of gene networks related to differentiation of MyoFb (e.g. paxilin and PAK) and reduced proliferation of non-p-MyoFb (e.g. cyclins and cell cycle regulation). Dedifferentiation of p-MyoFb with stress fibre de-polymerization, but not of non-p-MyoFb, was induced by SD-208 despite maintained stress. Stress fibre de-polymerization could also be induced by mechanical strain release in p-MyoFb and non-p-MyoFb (2-day cultures in unrestrained 3-D collagen matrices). Only p-MyoFb showed true dedifferentiation after long-term 3-D cultures. CONCLUSIONS: Fb, p-MyoFb, and non-p-MyoFb have a distinct gene expression, ultrastructural, and functional profile. Both reduction in mechanical strain and TGF-β-RI kinase inhibition can reverse p-MyoFb differentiation but not non-p-MyoFb. Oxford University Press 2014-03-01 2013-12-23 /pmc/articles/PMC3928002/ /pubmed/24368833 http://dx.doi.org/10.1093/cvr/cvt338 Text en © The Author 2013. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Driesen, Ronald B.
Nagaraju, Chandan K.
Abi-Char, Joëlle
Coenen, Tamara
Lijnen, Paul J.
Fagard, Robert H.
Sipido, Karin R.
Petrov, Victor V.
Reversible and irreversible differentiation of cardiac fibroblasts
title Reversible and irreversible differentiation of cardiac fibroblasts
title_full Reversible and irreversible differentiation of cardiac fibroblasts
title_fullStr Reversible and irreversible differentiation of cardiac fibroblasts
title_full_unstemmed Reversible and irreversible differentiation of cardiac fibroblasts
title_short Reversible and irreversible differentiation of cardiac fibroblasts
title_sort reversible and irreversible differentiation of cardiac fibroblasts
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928002/
https://www.ncbi.nlm.nih.gov/pubmed/24368833
http://dx.doi.org/10.1093/cvr/cvt338
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