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Article

Alveolar macrophage heterogeneity in idiopathic pulmonary fibrosis

2016-01-01

Abstract excerpt

Idiopathic Pulmonary Fibrosis (IPF) involves excess extracellular matrix (ECM) deposition within the lung interstitium, caused by non-resolving chronic inflammation and dysregulated repair. Alveolar macrophage (AMφ) may contribute to IPF through releasing various mediators by different subsets, investigated here in vitro, and ex vivo using a mouse model of bleomycin (BLM)-induced pulmonary fibrosis. The role of fo...

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Literature Corpus work
3af25ff6-9b1e-55bb-ab88-36a4b52e8c0f
DOI
10.25560/29433
Open publication

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