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ABSTRACT: Background
Reparative macrophages play a crucial role in limiting excessive fibrosis and promoting cardiac repair after myocardial infarction (MI), highlighting the significance of enhancing their reparative phenotype for wound healing. Metabolic adaptation orchestrates the phenotypic transition of macrophages; however, the precise mechanisms governing metabolic reprogramming of cardiac reparative macrophages remain poorly understood. In this study, we investigated the role of NPM1 (nucleophosmin 1) in the metabolic and phenotypic shift of cardiac macrophages in the context of MI and explored the therapeutic effect of targeting NPM1 for ischemic tissue repair.Methods
Peripheral blood mononuclear cells were obtained from healthy individuals and patients with MI to explore NP
SUBMITTER: Zhang S
PROVIDER: S-EPMC11175795 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature