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Trimaglio, G.* ; Mirtschink, P.* ; El-Armouche, A.* ; Chavakis, T.

Cardiac macrophages and their functions in homeostasis and injury.

Atherosclerosis 409:120480 (2025)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
Due to their remarkable plasticity, macrophages can adapt to diverse environments and challenges therein, thereby exerting tissue-specific and context-specific functions. Macrophages are the most frequent immune cell population present in the heart and contribute substantially to cardiac homeostasis and function. Moreover, macrophages are key regulators throughout all stages of heart injury, acquiring diverse phenotypes that can either ameliorate or exacerbate cardiac pathology in a context-dependent manner. The contribution of macrophages to both tissue damage as well as to recovery/tissue repair during heart injury provides avenues for therapeutic modulation of their functions to beneficially influence heart injury progression and hence prevent heart failure. However, to effectively fine-tune macrophage function, a deep understanding of their heterogeneity is required. The present review focuses on the phenotypic diversity and different roles of macrophages in cardiac homeostasis as well as in ischemic and non-ischemic heart disease, and discusses macrophages as potential therapeutic targets in the settings of heart injury.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Cardiac Injury ; Heart ; Inflammation ; Macrophages ; Tissue Repair; Matrix-metalloproteinase Expression; Marrow Mononuclear-cells; Myocardial-infarction; Heart-failure; Chemoattractant Protein-1; Electrical-conduction; Fetal Monocytes; Tyrosine Kinase; Ischemic-heart; Steady-state
Sprache englisch
Veröffentlichungsjahr 2025
HGF-Berichtsjahr 2025
ISSN (print) / ISBN 0021-9150
e-ISSN 1879-1484
Zeitschrift Atherosclerosis
Quellenangaben Band: 409, Heft: , Seiten: , Artikelnummer: 120480 Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Pancreatic Islet Research (IPI)
POF Topic(s) 90000 - German Center for Diabetes Research
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502600-008
Förderungen German Center for Child and Adolescent Health
Deutsche For-schungsgemeinschaft
DZG Innovation Funds
DOI 10.1016/j.atherosclerosis.2025.120480
WOS ID 001566982700001
Scopus ID 105015044746
PubMed ID 40913908
Erfassungsdatum 2025-10-28
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