• Eur Respir Rev · Jun 2018

    Review

    Matrix abnormalities in pulmonary fibrosis.

    • Chandak Upagupta, Chiko Shimbori, Rahmah Alsilmi, and Martin Kolb.
    • Firestone Institute for Respiratory Health, Dept of Medicine, McMaster University, Hamilton, ON, Canada.
    • Eur Respir Rev. 2018 Jun 30; 27 (148).

    AbstractIdiopathic pulmonary fibrosis (IPF) is a devastating, progressive disease, marked by excessive scarring, which leads to increased tissue stiffness, loss in lung function and ultimately death. IPF is characterised by progressive fibroblast and myofibroblast proliferation, and extensive deposition of extracellular matrix (ECM). Myofibroblasts play a key role in ECM deposition. Transforming growth factor (TGF)-β1 is a major growth factor involved in myofibroblast differentiation, and the creation of a profibrotic microenvironment. There is a strong link between increased ECM stiffness and profibrotic changes in cell phenotype and differentiation. The activation of TGF-β1 in response to mechanical stress from a stiff ECM explains some of the influence of the tissue microenvironment on cell phenotype and function. Understanding the close relationship between cells and their surrounding microenvironment will ultimately facilitate better management strategies for IPF.Copyright ©ERS 2018.

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