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Monocyte and macrophage differentiation: circulation inflammatory monocyte as biomarker for inflammatory diseases

TLDR
It is emphasized that inflammatory monocyte subsets are valuable biomarkers for inflammatory diseases, including cardiovascular diseases, as well as a potential mechanism for monocyte differentiation.
Abstract
Monocytes express various receptors, which monitor and sense environmental changes. Monocytes are highly plastic and heterogeneous, and change their functional phenotype in response to environmental stimulation. Evidence from murine and human studies has suggested that monocytosis can be an indicator of various inflammatory diseases. Monocytes can differentiate into inflammatory or anti-inflammatory subsets. Upon tissue damage or infection, monocytes are rapidly recruited to the tissue, where they can differentiate into tissue macrophages or dendritic cells. Given the rapid progress in monocyte research from broad spectrum of inflammatory diseases, there is a need to summarize our knowledge in monocyte heterogeneity and its impact in human disease. In this review, we describe the current understanding of heterogeneity of human and murine monocytes, the function of distinct subsets of monocytes, and a potential mechanism for monocyte differentiation. We emphasize that inflammatory monocyte subsets are valuable biomarkers for inflammatory diseases, including cardiovascular diseases.

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Monocytes and Macrophages in Pregnancy and Pre-Eclampsia

TL;DR: The role of monocytes and macrophages in the pathophysiology of pre-eclampsia is focused on and appears to be present in larger numbers and are also activated.
Journal ArticleDOI

A pan-cancer single-cell transcriptional atlas of tumor infiltrating myeloid cells.

TL;DR: A pan-cancer analysis of single myeloid cells from 210 patients across 15 human cancer types identified distinct features of TIMs across cancer types and suggested future avenues for rational, targeted immunotherapies.
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Properties and functions of adipose tissue macrophages in obesity.

TL;DR: This review will summarize the current understanding of the regulatory mechanisms of ATM function in relation to obesity, type 2 diabetes, depot of origin, and to other leukocytes such as AT dendritic cells, with hopes of emphasizing the regulatory nodes that can potentially be targeted to prevent and treat obesity‐related metabolic disorders.
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MiRNA-Mediated Macrophage Polarization and its Potential Role in the Regulation of Inflammatory Response.

TL;DR: Recent findings in miRNA expression profiles in polarized macrophages from murine and human sources are highlighted, and how these miRNAs regulate macrophage polarization is summarized.
References
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Journal ArticleDOI

Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties

TL;DR: Using a murine adoptive transfer system to probe monocyte homing and differentiation in vivo, two functional subsets among murine blood monocytes are identified: a short-lived CX(3)CR1(lo)CCR2(+)Gr1(+) subset that is actively recruited to inflamed tissues and a CX (3) CR1(hi)CCS1-dependent recruitment to noninflamed tissues.
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Fate Mapping Reveals Origins and Dynamics of Monocytes and Tissue Macrophages under Homeostasis

TL;DR: A fate-mapping study of the murine monocyte and macrophage compartment taking advantage of constitutive and conditional CX(3)CR1 promoter-driven Cre recombinase expression is reported, establishing that short-lived Ly6C(+) monocytes constitute obligatory steady-state precursors of blood-resident Ly 6C(-) cells and that the abundance of Ly6 C(+) blood monocytes dynamically controls the circulation lifespan of their progeny.
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The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions

TL;DR: This work identifies two distinct phases of monocyte participation after MI and proposes a model that reconciles the divergent properties of these cells in healing and identifies new therapeutic targets that can influence healing and ventricular remodeling after MI.
Journal ArticleDOI

Monitoring of blood vessels and tissues by a population of monocytes with patrolling behavior.

TL;DR: It is shown, by direct examination of blood monocyte functions in vivo, that a subset of monocytes patrols healthy tissues through long-range crawling on the resting endothelium, which initiated an early immune response and differentiated into macrophages.
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