Identification of a broadly fibrogenic macrophage subset induced by type 3 inflammation.
Humans
Mice
Animals
Granulocyte-Macrophage Colony-Stimulating Factor
/ metabolism
Transforming Growth Factor beta1
/ metabolism
Interleukin-17
/ metabolism
Pulmonary Fibrosis
/ metabolism
Cicatrix
Macrophages
/ pathology
Inflammation
/ pathology
Fatty Acid-Binding Proteins
/ metabolism
Membrane Glycoproteins
Receptors, Immunologic
Journal
Science immunology
ISSN: 2470-9468
Titre abrégé: Sci Immunol
Pays: United States
ID NLM: 101688624
Informations de publication
Date de publication:
14 04 2023
14 04 2023
Historique:
medline:
11
4
2023
entrez:
7
4
2023
pubmed:
8
4
2023
Statut:
ppublish
Résumé
Macrophages are central orchestrators of the tissue response to injury, with distinct macrophage activation states playing key roles in fibrosis progression and resolution. Identifying key macrophage populations found in human fibrotic tissues could lead to new treatments for fibrosis. Here, we used human liver and lung single-cell RNA sequencing datasets to identify a subset of
Identifiants
pubmed: 37027478
doi: 10.1126/sciimmunol.add8945
doi:
Substances chimiques
Granulocyte-Macrophage Colony-Stimulating Factor
83869-56-1
Transforming Growth Factor beta1
0
Interleukin-17
0
FABP5 protein, human
0
Fatty Acid-Binding Proteins
0
GPNMB protein, human
0
Membrane Glycoproteins
0
Trem2 protein, mouse
0
Receptors, Immunologic
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM