4.0 Article

IL-1β suppresses TGF-β-mediated myofibroblast differentiation in cardiac fibroblasts

期刊

GROWTH FACTORS
卷 31, 期 3, 页码 81-89

出版社

TAYLOR & FRANCIS LTD
DOI: 10.3109/08977194.2013.787994

关键词

Fibrosis; remodeling; transforming growth factor-beta; interleukin-1 beta

资金

  1. Odense University Hospital
  2. John and Birthe Meyer Foundation
  3. Danish Heart Association

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Cardiac fibrosis is a maladaptive response of the injured myocardium and is mediated through a complex interplay between molecular triggers and cellular responses. Interleukin (IL)-1 beta is a key inflammatory inducer in cardiac disease and promotes cell invasion and cardiomyocyte injury, but little is known of its impact on fibrosis. A major cornerstone of fibrosis is the differentiation of cardiac fibroblasts (CFs) into myofibroblasts (myoFbs), which is highly promoted by Transforming Growth Factor (TGF)-beta. Therefore, we asked how IL-1 beta functionally modulated CF-to-myoFb differentiation. Using a differentiation model of ventricular fibroblasts, we found that IL-1 beta instigated substantial anti-fibrogenic effects. In specific, IL-1 beta reduced proliferation, matrix activity, cell motility and a-smooth muscle actin expression, which are all hallmarks of myoFb differentiation. These findings suggest that IL-1 beta, besides from its acknowledged adverse role in the inflammatory response, can also exert beneficial effects in cardiac fibrosis by actively suppressing differentiation of CFs into fibrogenic myoFbs.

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