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The extracellular matrix protein periostin is required for wound repair in primary human airway epithelia
Journal article   Open access   Peer reviewed

The extracellular matrix protein periostin is required for wound repair in primary human airway epithelia

Lorena A Tran, Michael Catlin, Scott Schecter, Andrew L Thurman, Shreya Ghimire, Rosarie Tudas, Brandon Bettis, Ryan Gannon, Joseph Zabner and Alejandro A Pezzulo
American journal of physiology. Lung cellular and molecular physiology, Vol.328(6), pp.L826-L831
06/01/2025
DOI: 10.1152/ajplung.00039.2025
PMCID: PMC12100768
PMID: 40257107
url
https://doi.org/10.1152/ajplung.00039.2025View
Published (Version of record) Open Access

Abstract

Type 2 inflammation and epithelial-to-mesenchymal transitions (EMTs) play critical roles in airway repair after damage from allergens or parasites. The matricellular protein periostin (POSTN) has increased expression in inflammatory conditions and has been implicated in fibrosis and EMT, suggesting a role in airway repair. This study investigates the role of periostin in airway epithelial and lung fibroblast wound repair using an wound model. Our results demonstrate that the type 2 cytokine IL-13 induces periostin secretion from primary human airway epithelial basal cells. Periostin knockdown in human airway epithelial cells (HAEs) and human lung fibroblasts (HLFs) impairs wound closure, indicating that periostin is required for airway repair. In a coculture model of HAE and HLFs, fibroblast-secreted POSTN is required for airway epithelial wound repair, suggesting that periostin is involved in paracrine signaling between the two cell types. These findings highlight periostin's critical function in epithelial and fibroblast-mediated wound repair, suggesting its potential as a therapeutic target for diseases characterized by aberrant wound healing and fibrosis, such as asthma and idiopathic pulmonary fibrosis.
Inflammation human airway epithelia fibrosis wound repair periostin

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