Alveolar Lipid–Macrophage Networks at the Intersection of Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is characterised by progressive parenchymal remodelling, driven by epithelial dysfunction, fibroblast activation, and altered immune regulation within the distal lung. Alveolar macrophages (AMs) reside in a surfactant-rich environment and are specialised for conti...

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Prif Awduron:	Simon H. Apte, Viviana P. Lutzky, Penny L. Groves, Daniel C. Chambers
Fformat:	Artigo
Iaith:	Inglês
Cyhoeddwyd:	MDPI AG 2026-04-01
Cyfres:	Cells
Pynciau:	idiopathic pulmonary fibrosis alveolar macrophages lipid metabolism surfactant homeostasis macrophage heterogeneity cholesterol handling
Mynediad Ar-lein:	https://www.mdpi.com/2073-4409/15/8/668
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