Resident and recruited macrophages differentially contribute to cardiac healing after myocardial ischemia.
developmental biology
immunology
inflammation
macrophage
mouse
myocardial infarction
Journal
eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614
Informations de publication
Date de publication:
22 May 2024
22 May 2024
Historique:
medline:
22
5
2024
pubmed:
22
5
2024
entrez:
22
5
2024
Statut:
epublish
Résumé
Cardiac macrophages are heterogenous in phenotype and functions, which has been associated with differences in their ontogeny. Despite extensive research, our understanding of the precise role of different subsets of macrophages in ischemia/reperfusion (I/R) injury remains incomplete. We here investigated macrophage lineages and ablated tissue macrophages in homeostasis and after I/R injury in a CSF1R-dependent manner. Genomic deletion of a fms-intronic regulatory element (FIRE) in the
Identifiants
pubmed: 38775664
doi: 10.7554/eLife.89377
pii: 89377
doi:
pii:
Substances chimiques
Csf1r protein, mouse
0
Banques de données
GEO
['GSE263544', 'GSE263545']
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Deutsches Zentrum für Herz-Kreislaufforschung
ID : 81Z0600204
Organisme : Deutsches Zentrum für Herz-Kreislaufforschung
ID : 81X2600252
Organisme : Deutsches Zentrum für Herz-Kreislaufforschung
ID : 81X2600256
Organisme : Deutsche Forschungsgemeinschaft
ID : SCHU 2297/1-1
Organisme : Deutsche Forschungsgemeinschaft
ID : SFB 1123 project Z02
Organisme : Deutsche Forschungsgemeinschaft
ID : SFB 1123 project A07
Organisme : Deutsche Forschungsgemeinschaft
ID : SFB TRR332, project A06
Organisme : European Society of Cardiology
ID : Research Grant 2021
Informations de copyright
© 2023, Weinberger et al.
Déclaration de conflit d'intérêts
TW, MD, MJ, MF, CG, KK, VW, SA, SR, JF, LL, WL, JW, JL, LT, DE, GP, SM, AH, CW, SE, AT, RZ, CP, EG, CS No competing interests declared