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ID 7469
Class Mammalia
Species Mouse
Tissue Lung
Sample Tissue
Disease type Asbestos-Induced Pulmonary Fibrosis
Cell type Macrophages
Cell type (subtype) Alveolar macrophages2
Cell marker Car4, Chil3, Ctsk, S100A1, Wfdc21
Frequency
PubMed ID 31601718
Journal Eur Respir J
SCI IF 12.336
Evidence Alveolar macrophages from cluster AM1 were characterised by expression of genes associated with normal homeostatic function of alveolar macrophages (Ear1 and Fabp1) (supplementary figure S4d). Macrophages from cluster AM2 expressed genes involved in the inflammatory response, cytokine production and matrix metalloproteinase activation (Car4, Ctsk, Chil3, S100a1 and Wfdc21) (supplementary figure S4d). In agreement with fate mapping studies, macrophages from cluster AM3 exhibited a more immature alveolar macrophage phenotype, characterised by lower expression of Pparg, Car4, Ear1, Siglecf and Marco, increased expression of Itgam, Cd36 and Gpnmb (supplementary figure S4c and d)
Title A spatially restricted fibrotic niche in pulmonary fibrosis is sustained by M-CSF/M-CSFR signalling in monocyte-derived alveolar macrophages
Authors Nikita Joshi et al.
Date 2020.1
Data available NA