| Literature DB >> 33763066 |
Chunye Zhang1, Ming Yang2, Aaron C Ericsson1,3,4.
Abstract
Tissue-resident macrophages (TRMs) are heterogeneous populations originating either from monocytes or embryonic progenitors, and distribute in lymphoid and non-lymphoid tissues. TRMs play diverse roles in many physiological processes, including metabolic function, clearance of cellular debris, and tissue remodeling and defense. Macrophages can be polarized to different functional phenotypes depending on their origin and tissue microenvironment. Specific macrophage subpopulations are associated with disease progression. In studies of fate-mapping and single-cell RNA sequencing methodologies, several critical molecules have been identified to induce the change of macrophage function. These molecules are potential markers for diagnosis and selective targets for novel macrophage-mediated treatment. In this review, we discuss some of the recent findings regarding less-known molecules and new functions of well-known molecules. Understanding the mechanisms of these molecules in macrophages has the potential to yield new macrophage-mediated treatments or diagnostic approaches to disease.Entities:
Keywords: diagnostic marker; macrophage; molecules; phenotype; therapy
Year: 2021 PMID: 33763066 PMCID: PMC7982479 DOI: 10.3389/fimmu.2021.620510
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561