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Title: Sex-Related Differences in Murine Models of Chemically Induced Pulmonary Fibrosis.

Authors: Solopov, Pavel; Colunga Biancatelli, Ruben Manuel Luciano; Dimitropoulou, Christiana; Catravas, John D

Published In Int J Mol Sci, (2021 May 31)

Abstract: We developed two models of chemically induced chronic lung injury and pulmonary fibrosis in mice (intratracheally administered hydrochloric acid (HCl) and intratracheally administered nitrogen mustard (NM)) and investigated male-female differences. Female mice exhibited higher 30-day survival and less weight loss than male mice. Thirty days after the instillation of either HCl or NM, bronchoalveolar lavage fluid displayed a persistent, mild inflammatory response, but with higher white blood cell numbers and total protein content in males vs. females. Furthermore, females exhibited less collagen deposition, milder pulmonary fibrosis, and lower Ashcroft scores. After instillation of either HCl or NM, all animals displayed increased values of phosphorylated (activated) Heat Shock Protein 90, which plays a crucial role in the alveolar wound-healing processes; however, females presented lower activation of both transforming growth factor-β (TGF-β) signaling pathways: ERK and SMAD. We propose that female mice are protected from chronic complications of a single exposure to either HCl or NM through a lesser activation of TGF-β and downstream signaling. The understanding of the molecular mechanisms that confer a protective effect in females could help develop new, gender-specific therapeutics for IPF.

PubMed ID: 34072833 Exiting the NIEHS site

MeSH Terms: Animals; Collagen/genetics*; Female; Gene Expression Regulation/genetics; HSP90 Heat-Shock Proteins/genetics*; Humans; Hydrochloric Acid/toxicity; Idiopathic Pulmonary Fibrosis/chemically induced; Idiopathic Pulmonary Fibrosis/genetics*; Idiopathic Pulmonary Fibrosis/pathology; Lung/pathology; MAP Kinase Signaling System/genetics; Male; Mechlorethamine/toxicity; Mice; Smad Proteins/genetics; Transforming Growth Factor beta/genetics*

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