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Inhibiting Fibroblast Mechanotransduction Modulates Severity of Idiopathic Pulmonary Fibrosis

Artem A. Trotsyuk, Kellen Chen, Sun Hyung, Kun Ma, Dominic Henn, Alana M. Mermin-Bunnell, Smiti Mittal, Jagannath Padmanabhan, Madelyn R. Larson, Sydney R. Steele, Dharshan Sivaraj, Clark A. Bonham, Chikage Noishiki, Mélanie Rodrigues, Yuanwen Jiang, Serena L. Jing, Simiao Niu, Arhana Chattopadhyay, David Perrault, Melissa C. Leeolou, Katharina S. Fischer, Gurupranav Gurusankar, Hudson C. Kussie, Derrick C. Wan, Michael Januszyk, Michael T. Longaker, Geoffrey C. Gurtner

2021Advances in Wound Care16 citationsDOI

Abstract

Objective: Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease that affects 63 in every 100,000 Americans. Its etiology remains unknown, although inflammatory pathways appear to be important. Given the dynamic environment of the lung, we examined the significance of mechanotransduction on both inflammatory and fibrotic signaling during IPF.

Topics & Concepts

Idiopathic pulmonary fibrosisMechanotransductionFibrosisPulmonary fibrosisFocal adhesionMedicineMyofibroblastLungFibroblastProinflammatory cytokinePathologyCancer researchBleomycinContext (archaeology)InflammationSignal transductionBiologyCell biologyImmunologyInternal medicineCell culturePaleontologyGeneticsChemotherapyInterstitial Lung Diseases and Idiopathic Pulmonary FibrosisOccupational and environmental lung diseasesPleural and Pulmonary Diseases
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