The Ski-Zeb2-Meox2 pathway provides a novel mechanism for regulation of the cardiac myofibroblast phenotype
| Autor: | Saeid Ghavami, Jared J.L. Davies, Krista L. Filomeno, Jeffrey T. Wigle, Ryan H. Cunnington, Ian M.C. Dixon, Josette M. Northcott, Fahmida Jahan, Morvarid S. Kavosh |
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| Rok vydání: | 2013 |
| Předmět: |
Cardiac fibrosis
Mutant Myocardial Infarction Muscle Proteins Biology Rats Sprague-Dawley Fibrosis Proto-Oncogene Proteins medicine Animals Protein Isoforms RNA Messenger Myofibroblasts Molecular Biology Psychological repression Zinc Finger E-box Binding Homeobox 2 Homeodomain Proteins Messenger RNA Mechanism (biology) Myocardium Zinc Finger E-box-Binding Homeobox 1 Cell Differentiation Cell Biology Fibroblasts medicine.disease Phenotype Cell biology Rats Repressor Proteins Gene Expression Regulation Cancer research sense organs Myofibroblast Function (biology) Developmental Biology Signal Transduction Transcription Factors |
| Zdroj: | Journal of cell science. 127(Pt 1) |
| ISSN: | 1477-9137 |
| Popis: | Cardiac fibrosis is linked to fibroblast-to-myofibroblast phenoconversion and proliferation but the mechanisms underlying this are poorly understood. Ski is a negative regulator of TGF-β-Smad signaling in myofibroblasts, and might redirect the myofibroblast phenotype back to fibroblasts. Meox2 could alter TGF-β-mediated cellular processes and is repressed by Zeb2. Here, we investigated whether Ski diminishes the myofibroblast phenotype by de-repressing Meox2 expression and function through repression of Zeb2 expression. We show that expression of Meox1 and Meox2 mRNA and Meox2 protein is reduced during phenoconversion of fibroblasts to myofibroblasts. Overexpression of Meox2 shifts the myofibroblasts into fibroblasts, whereas the Meox2 DNA-binding mutant has no effect on myofibroblast phenotype. Overexpression of Ski partially restores Meox2 mRNA expression levels to those in cardiac fibroblasts. Expression of Zeb2 increased during phenoconversion and Ski overexpression reduces Zeb2 expression in first-passage myofibroblasts. Furthermore, expression of Meox2 is decreased in scar following myocardial infarction, whereas Zeb2 protein expression increases in the infarct scar. Thus Ski modulates the cardiac myofibroblast phenotype and function through suppression of Zeb2 by upregulating the expression of Meox2. This cascade might regulate cardiac myofibroblast phenotype and presents therapeutic options for treatment of cardiac fibrosis. |
| Databáze: | OpenAIRE |
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