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      Macrophage Immunometabolism and Inflammaging: Roles of Mitochondrial Dysfunction, Cellular Senescence, CD38, and NAD

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          Abstract

          Aging is a complex process that involves dysfunction on multiple levels, all of which seem to converge on inflammation. Macrophages are intimately involved in initiating and resolving inflammation, and their dysregulation with age is a primary contributor to inflammaging—a state of chronic, low-grade inflammation that develops during aging. Among the age-related changes that occur to macrophages are a heightened state of basal inflammation and diminished or hyperactive inflammatory responses, which seem to be driven by metabolic-dependent epigenetic changes. In this review article we provide a brief overview of mitochondrial functions and age-related changes that occur to macrophages, with an emphasis on how the inflammaging environment, senescence, and NAD decline can affect their metabolism, promote dysregulation, and contribute to inflammaging and age-related pathologies.

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          Most cited references118

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          Understanding the Mysterious M2 Macrophage through Activation Markers and Effector Mechanisms

          The alternatively activated or M2 macrophages are immune cells with high phenotypic heterogeneity and are governing functions at the interface of immunity, tissue homeostasis, metabolism, and endocrine signaling. Today the M2 macrophages are identified based on the expression pattern of a set of M2 markers. These markers are transmembrane glycoproteins, scavenger receptors, enzymes, growth factors, hormones, cytokines, and cytokine receptors with diverse and often yet unexplored functions. This review discusses whether these M2 markers can be reliably used to identify M2 macrophages and define their functional subdivisions. Also, it provides an update on the novel signals of the tissue environment and the neuroendocrine system which shape the M2 activation. The possible evolutionary roots of the M2 macrophage functions are also discussed.
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            Mitochondrial Dysfunction Induces Senescence with a Distinct Secretory Phenotype.

            Cellular senescence permanently arrests cell proliferation, often accompanied by a multi-faceted senescence-associated secretory phenotype (SASP). Loss of mitochondrial function can drive age-related declines in the function of many post-mitotic tissues, but little is known about how mitochondrial dysfunction affects mitotic tissues. We show here that several manipulations that compromise mitochondrial function in proliferating human cells induce a senescence growth arrest with a modified SASP that lacks the IL-1-dependent inflammatory arm. Cells that underwent mitochondrial dysfunction-associated senescence (MiDAS) had lower NAD+/NADH ratios, which caused both the growth arrest and prevented the IL-1-associated SASP through AMPK-mediated p53 activation. Progeroid mice that rapidly accrue mtDNA mutations accumulated senescent cells with a MiDAS SASP in vivo, which suppressed adipogenesis and stimulated keratinocyte differentiation in cell culture. Our data identify a distinct senescence response and provide a mechanism by which mitochondrial dysfunction can drive aging phenotypes.
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              α-ketoglutarate orchestrates macrophage activation through metabolic and epigenetic reprogramming

              Glutamine metabolism provides synergistic support for macrophage activation and elicitation of desirable immune responses; however, the underlying mechanisms regulated by glutamine metabolism to orchestrate macrophage activation remain unclear. Here we show that the production of α-ketoglutarate (αKG) via glutaminolysis is important for alternative (M2) activation of macrophages, including engagement of fatty acid oxidation (FAO) and Jmjd3-dependent epigenetic reprogramming of M2 genes. This M2-promoting mechanism is further modulated by a high αKG/succinate ratio, whereas a low ratio strengthens the proinflammatory phenotype in classically activated (M1) macrophages. As such, αKG contributes to endotoxin tolerance after M1 activation. This study reveals new mechanistic regulations by which glutamine metabolism tailors the immune responses of macrophages through metabolic and epigenetic reprogramming.
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                Author and article information

                Journal
                101607751
                41320
                Immunometabolism
                Immunometabolism
                Immunometabolism
                2084-6835
                9 July 2020
                1 July 2020
                2020
                06 August 2020
                : 2
                : 3
                : e200026
                Affiliations
                [1 ]School of Health Studies, University of Memphis, Memphis, TN 38152, USA
                [2 ]Bioinformatics Program, University of Memphis, Memphis, TN 38152, USA
                [3 ]Center for Nutraceutical and Dietary Supplement Research, University of Memphis, Memphis, TN 38152, USA
                Author notes

                AUTHOR CONTRIBUTIONS

                JY and BP outlined the paper. JY, RE, BP wrote the paper. JY and BP edited and revised the paper. All authors approved the final submission.

                [* ]Correspondence: Brandt D. Pence, bdpence@ 123456memphis.edu ; Tel.: +1-901-678-4316.
                Article
                HRAMS1609164
                10.20900/immunometab20200026
                7409778
                32774895
                c687079f-ac90-4321-91fb-9c111f5ffa1c

                This is an open access article distributed under the terms and conditions of Creative Commons Attribution 4.0 International License.

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                Categories
                Article

                aging,macrophage,monocyte,nad,mitochondria,inflammaging,immunometabolism,senescence,sasp,cd38

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