| Literature DB >> 32596871 |
Xiaoyun Li1, Sharon E Kim1, Ting-Yun Chen1,2, Juan Wang1,3, Xia Yang1,3, Tracy Tabib4, Jiangning Tan1, Brandon Guo1, Sonia Fung1, Jing Zhao5, John Sembrat1, Mauricio Rojas1, Sruti Shiva6, Robert Lafyatis4, Claudette St Croix7, Jonathan K Alder1, Y Peter Di8, Daniel J Kass1, Yingze Zhang1,9.
Abstract
Idiopathic pulmonary fibrosis (IPF) is characterized by altered epithelial cell phenotypes, which are associated with myofibroblast accumulation in the lung. Atypical alveolar epithelial cells in IPF express molecular markers of airway epithelium. Polymorphisms within and around Toll interacting protein (TOLLIP) are associated with the susceptibility to IPF and mortality. However, the functional role of TOLLIP in IPF is unknown. Using lung tissues from IPF and control subjects, we showed that expression of TOLLIP gene in the lung parenchyma is globally lower in IPF compared to controls. Lung cells expressing significant levels of TOLLIP include macrophages, alveolar type II, and basal cells. TOLLIP protein expression is lower in the parenchyma of IPF lungs but is expressed in the atypical epithelial cells of the distal fibrotic regions. Using overexpression and silencing approaches, we demonstrate that TOLLIP protects cells from bleomycin-induced apoptosis using primary bronchial epithelial cells and BEAS-2B cells. The protective effects are mediated by reducing mitochondrial reactive oxygen species (ROS) levels and upregulating autophagy. Therefore, global downregulation of the TOLLIP gene in IPF lungs may predispose injured lung epithelial cells to apoptosis and to the development of IPF.Entities:
Keywords: TOLLIP; apoptosis; autophagy; basal cells; idiopathic pulmonary fibrosis; lung epithelial cells
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Year: 2020 PMID: 32596871 PMCID: PMC8175118 DOI: 10.1096/fj.201902636RR
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191