» Articles » PMID: 37240103

Monocyte Differentiation and Heterogeneity: Inter-Subset and Interindividual Differences

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 May 27
PMID 37240103
Authors
Affiliations
Soon will be listed here.
Abstract

The three subsets of human monocytes, classical, intermediate, and nonclassical, show phenotypic heterogeneity, particularly in their expression of CD14 and CD16. This has enabled researchers to delve into the functions of each subset in the steady state as well as in disease. Studies have revealed that monocyte heterogeneity is multi-dimensional. In addition, that their phenotype and function differ between subsets is well established. However, it is becoming evident that heterogeneity also exists within each subset, between health and disease (current or past) states, and even between individuals. This realisation casts long shadows, impacting how we identify and classify the subsets, the functions we assign to them, and how they are examined for alterations in disease. Perhaps the most fascinating is evidence that, even in relative health, interindividual differences in monocyte subsets exist. It is proposed that the individual's microenvironment could cause long-lasting or irreversible changes to monocyte precursors that echo to monocytes and through to their derived macrophages. Here, we will discuss the types of heterogeneity recognised in monocytes, the implications of these for monocyte research, and most importantly, the relevance of this heterogeneity for health and disease.

Citing Articles

Modulation of NCX1 expression in monocytes associates with multiple sclerosis progression.

Rubino V, Cammarota M, Criscuolo C, Cianflone A, De Martino M, de Rosa V Heliyon. 2025; 11(4):e42332.

PMID: 40041001 PMC: 11876900. DOI: 10.1016/j.heliyon.2025.e42332.


Single-cell transcriptome analysis reveals the dysregulated monocyte state associated with tuberculosis progression.

Ma R, Yang W, Guo W, Zhang H, Wang Z, Ge Z BMC Infect Dis. 2025; 25(1):210.

PMID: 39939918 PMC: 11823163. DOI: 10.1186/s12879-025-10612-3.


Inflammatory Monocyte Subsets Correlation with Iron Levels in Low Vitamin D Pediatric Transfusion-Dependent Thalassemia.

Ghozali M, Matahari M, Cahyadi A, Agustini S, Ghrahani R, Reniarti L J Inflamm Res. 2025; 18():421-429.

PMID: 39802505 PMC: 11725247. DOI: 10.2147/JIR.S476688.


Monocytes across life span in HIV infection: lights and shadows.

Neri A, Olivieri G, Pighi C, Amodio D, Cotugno N, Palma P Curr Opin HIV AIDS. 2025; 20(2):133-144.

PMID: 39774439 PMC: 11809736. DOI: 10.1097/COH.0000000000000910.


Modulation of Monocyte Effector Functions and Gene Expression by Human Cytomegalovirus Infection.

Planchon M, Fishman J, El Khoury J Viruses. 2025; 16(12.

PMID: 39772120 PMC: 11680302. DOI: 10.3390/v16121809.


References
1.
Ancuta P, Rao R, Moses A, Mehle A, Shaw S, Luscinskas F . Fractalkine preferentially mediates arrest and migration of CD16+ monocytes. J Exp Med. 2003; 197(12):1701-7. PMC: 2193954. DOI: 10.1084/jem.20022156. View

2.
MEURET G, Bammert J, Hoffmann G . Kinetics of human monocytopoiesis. Blood. 1974; 44(6):801-16. View

3.
Ligi D, Lo Sasso B, Henry B, Ciaccio M, Lippi G, Plebani M . Deciphering the role of monocyte and monocyte distribution width (MDW) in COVID-19: an updated systematic review and meta-analysis. Clin Chem Lab Med. 2023; 61(6):960-973. DOI: 10.1515/cclm-2022-0936. View

4.
Ruiz-Limon P, Ortega-Castro R, Barbarroja N, Perez-Sanchez C, Jamin C, Patino-Trives A . Molecular Characterization of Monocyte Subsets Reveals Specific and Distinctive Molecular Signatures Associated With Cardiovascular Disease in Rheumatoid Arthritis. Front Immunol. 2019; 10:1111. PMC: 6536567. DOI: 10.3389/fimmu.2019.01111. View

5.
Wenzel P, Rossmann H, Muller C, Kossmann S, Oelze M, Schulz A . Heme oxygenase-1 suppresses a pro-inflammatory phenotype in monocytes and determines endothelial function and arterial hypertension in mice and humans. Eur Heart J. 2015; 36(48):3437-46. DOI: 10.1093/eurheartj/ehv544. View