| Literature DB >> 25527499 |
Krishna K Singh1, Fina Lovren2, Yi Pan2, Adrian Quan2, Azza Ramadan2, Pratiek N Matkar3, Mehroz Ehsan2, Paul Sandhu2, Laura E Mantella2, Nandini Gupta2, Hwee Teoh4, Matteo Parotto5, Arata Tabuchi6, Wolfgang M Kuebler7, Mohammed Al-Omran8, Toren Finkel9, Subodh Verma10.
Abstract
Pulmonary fibrosis is a progressive disease characterized by fibroblast proliferation and excess deposition of collagen and other extracellular matrix components. Although the origin of fibroblasts is multifactorial, recent data implicate endothelial-to-mesenchymal transition as an important source of fibroblasts. We report herein that loss of the essential autophagy gene ATG7 in endothelial cells (ECs) leads to impaired autophagic flux accompanied by marked changes in EC architecture, loss of endothelial, and gain of mesenchymal markers consistent with endothelial-to-mesenchymal transition. Loss of ATG7 also up-regulates TGFβ signaling and key pro-fibrotic genes in vitro. In vivo, EC-specific ATG7 knock-out mice exhibit a basal reduction in endothelial-specific markers and demonstrate an increased susceptibility to bleomycin-induced pulmonary fibrosis and collagen accumulation. Our findings help define the role of endothelial autophagy as a potential therapeutic target to limit organ fibrosis, a condition for which presently there are no effective available treatments.Entities:
Keywords: Autophagy; Autophagy-related Protein 7 (ATG7); Endothelial Cell; Endothelial-to-mesenchymal Transition; Gene Silencing; Pulmonary Fibrosis
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Year: 2014 PMID: 25527499 PMCID: PMC4317030 DOI: 10.1074/jbc.M114.604603
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157