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      Mitochondrial metabolism regulates macrophage biology

      review-article
      , , ,
      The Journal of Biological Chemistry
      American Society for Biochemistry and Molecular Biology
      mitochondrial metabolism, macrophage activation, macrophage biology, mitochondrial dysfunction, oxidative stress, α-KG, α-ketoglutarate, ΔΨm, mitochondrial membrane potential, ACLY, ATP citrate lyase, AMPK, AMP-activated protein kinase, AST, aspartate aminotransferase, CIC, mitochondrial citrate carrier, DAMPs, damage-associated molecular patterns, Drp1, dynamin-related protein 1, DMF, Dimethyl fumarate, ETC, electron transport chain, eIF5A, hypusination of translation factor eukaryotic initiation factor 5A, ER, endoplasmic reticulum, FAO, fatty acid oxidation, FADH2, flavin adenine dinucleotide hydride, GABA, γ-amino butyric acid, GAD, glutamic acid decarboxylase, GAPDH, glycolytic enzyme glyceraldehyde 3-phosphate dehydrogenase, GSDMD, gasdermin D, HIF-1α, hypoxia inducible factor 1α, HMGB1, high mobility group box 1, IDH, isocitrate dehydrogenase, IFNγ, interferon-γ, IL-4, interleukin-4, iNOS, inducible nitric oxide synthase, IRG1, Immune-Responsive Gene 1, KLF4, Krüppel-like factor 4, LPS, lipopolysaccharide, MAS, malate-aspartate shuttle, MDVs, mitochondria-derived vesicles, MHC, Major Histocompatibility Complex, mTOR, mammalian target of rapamycin, mtROS, mitochondrial reactive oxygen species, NADH, adenine diphosphate hydride, NF-κB, nuclear factor kappa B, NLRP3, NOD-, LRR- and pyrin domain-containing 3, NO, nitric oxide, OAA, oxaloacetate, oxPAPC, 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphorylcholine, OXPHOS, oxidative phosphorylation, PAMPs, pathogen-associated molecular patterns, PARP, Poly (ADP-ribose) polymerase, PGE2, Prostaglandin E2, PHD, prolyl hydroxylases, PPAR, peroxisome proliferator-activated receptor, RET, reverse electron transport, SDH, succinate dehydrogenase, SIRT, Sirtuin, SUCLG1, succinyl-CoA synthetase, SUCNR1, succinate receptor 1, TCA, tricarboxylic acid, TLR, Toll-like receptor, UPR, unfolded protein response

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          Abstract

          Mitochondria are critical for regulation of the activation, differentiation, and survival of macrophages and other immune cells. In response to various extracellular signals, such as microbial or viral infection, changes to mitochondrial metabolism and physiology could underlie the corresponding state of macrophage activation. These changes include alterations of oxidative metabolism, mitochondrial membrane potential, and tricarboxylic acid (TCA) cycling, as well as the release of mitochondrial reactive oxygen species (mtROS) and mitochondrial DNA (mtDNA) and transformation of the mitochondrial ultrastructure. Here, we provide an updated review of how changes in mitochondrial metabolism and various metabolites such as fumarate, succinate, and itaconate coordinate to guide macrophage activation to distinct cellular states, thus clarifying the vital link between mitochondria metabolism and immunity. We also discuss how in disease settings, mitochondrial dysfunction and oxidative stress contribute to dysregulation of the inflammatory response. Therefore, mitochondria are a vital source of dynamic signals that regulate macrophage biology to fine-tune immune responses.

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          Macrophage plasticity, polarization, and function in health and disease.

          Macrophages are heterogeneous and their phenotype and functions are regulated by the surrounding micro-environment. Macrophages commonly exist in two distinct subsets: 1) Classically activated or M1 macrophages, which are pro-inflammatory and polarized by lipopolysaccharide (LPS) either alone or in association with Th1 cytokines such as IFN-γ, GM-CSF, and produce pro-inflammatory cytokines such as interleukin-1β (IL-1β), IL-6, IL-12, IL-23, and TNF-α; and 2) Alternatively activated or M2 macrophages, which are anti-inflammatory and immunoregulatory and polarized by Th2 cytokines such as IL-4 and IL-13 and produce anti-inflammatory cytokines such as IL-10 and TGF-β. M1 and M2 macrophages have different functions and transcriptional profiles. They have unique abilities by destroying pathogens or repair the inflammation-associated injury. It is known that M1/M2 macrophage balance polarization governs the fate of an organ in inflammation or injury. When the infection or inflammation is severe enough to affect an organ, macrophages first exhibit the M1 phenotype to release TNF-α, IL-1β, IL-12, and IL-23 against the stimulus. But, if M1 phase continues, it can cause tissue damage. Therefore, M2 macrophages secrete high amounts of IL-10 and TGF-β to suppress the inflammation, contribute to tissue repair, remodeling, vasculogenesis, and retain homeostasis. In this review, we first discuss the basic biology of macrophages including origin, differentiation and activation, tissue distribution, plasticity and polarization, migration, antigen presentation capacity, cytokine and chemokine production, metabolism, and involvement of microRNAs in macrophage polarization and function. Secondly, we discuss the protective and pathogenic role of the macrophage subsets in normal and pathological pregnancy, anti-microbial defense, anti-tumor immunity, metabolic disease and obesity, asthma and allergy, atherosclerosis, fibrosis, wound healing, and autoimmunity.
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            Exploring the full spectrum of macrophage activation.

            Macrophages display remarkable plasticity and can change their physiology in response to environmental cues. These changes can give rise to different populations of cells with distinct functions. In this Review we suggest a new grouping of macrophage populations based on three different homeostatic activities - host defence, wound healing and immune regulation. We propose that similarly to primary colours, these three basic macrophage populations can blend into various other 'shades' of activation. We characterize each population and provide examples of macrophages from specific disease states that have the characteristics of one or more of these populations.
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              How mitochondria produce reactive oxygen species

              The production of ROS (reactive oxygen species) by mammalian mitochondria is important because it underlies oxidative damage in many pathologies and contributes to retrograde redox signalling from the organelle to the cytosol and nucleus. Superoxide (O2 •−) is the proximal mitochondrial ROS, and in the present review I outline the principles that govern O2 •− production within the matrix of mammalian mitochondria. The flux of O2 •− is related to the concentration of potential electron donors, the local concentration of O2 and the second-order rate constants for the reactions between them. Two modes of operation by isolated mitochondria result in significant O2 •− production, predominantly from complex I: (i) when the mitochondria are not making ATP and consequently have a high Δp (protonmotive force) and a reduced CoQ (coenzyme Q) pool; and (ii) when there is a high NADH/NAD+ ratio in the mitochondrial matrix. For mitochondria that are actively making ATP, and consequently have a lower Δp and NADH/NAD+ ratio, the extent of O2 •− production is far lower. The generation of O2 •− within the mitochondrial matrix depends critically on Δp, the NADH/NAD+ and CoQH2/CoQ ratios and the local O2 concentration, which are all highly variable and difficult to measure in vivo. Consequently, it is not possible to estimate O2 •− generation by mitochondria in vivo from O2 •−-production rates by isolated mitochondria, and such extrapolations in the literature are misleading. Even so, the description outlined here facilitates the understanding of factors that favour mitochondrial ROS production. There is a clear need to develop better methods to measure mitochondrial O2 •− and H2O2 formation in vivo, as uncertainty about these values hampers studies on the role of mitochondrial ROS in pathological oxidative damage and redox signalling.
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                Author and article information

                Contributors
                Journal
                J Biol Chem
                J Biol Chem
                The Journal of Biological Chemistry
                American Society for Biochemistry and Molecular Biology
                0021-9258
                1083-351X
                23 June 2021
                July 2021
                23 June 2021
                : 297
                : 1
                : 100904
                Affiliations
                [1]School of Life Science and Technology, ShanghaiTech University, Shanghai, China
                Author notes
                []For correspondence: Tiffany Horng; Yafang Wang wangyf2@ 123456shanghaitech.edu.cn tsyhorng@ 123456shanghaitech.edu.cn
                Article
                S0021-9258(21)00704-3 100904
                10.1016/j.jbc.2021.100904
                8294576
                34157289
                c17436d4-3742-49ce-8cd8-9064ba14b1d8
                © 2021 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 November 2020
                : 16 June 2021
                Categories
                JBC Reviews

                Biochemistry
                mitochondrial metabolism,macrophage activation,macrophage biology,mitochondrial dysfunction,oxidative stress,α-kg, α-ketoglutarate,δψm, mitochondrial membrane potential,acly, atp citrate lyase,ampk, amp-activated protein kinase,ast, aspartate aminotransferase,cic, mitochondrial citrate carrier,damps, damage-associated molecular patterns,drp1, dynamin-related protein 1,dmf, dimethyl fumarate,etc, electron transport chain,eif5a, hypusination of translation factor eukaryotic initiation factor 5a,er, endoplasmic reticulum,fao, fatty acid oxidation,fadh2, flavin adenine dinucleotide hydride,gaba, γ-amino butyric acid,gad, glutamic acid decarboxylase,gapdh, glycolytic enzyme glyceraldehyde 3-phosphate dehydrogenase,gsdmd, gasdermin d,hif-1α, hypoxia inducible factor 1α,hmgb1, high mobility group box 1,idh, isocitrate dehydrogenase,ifnγ, interferon-γ,il-4, interleukin-4,inos, inducible nitric oxide synthase,irg1, immune-responsive gene 1,klf4, krüppel-like factor 4,lps, lipopolysaccharide,mas, malate-aspartate shuttle,mdvs, mitochondria-derived vesicles,mhc, major histocompatibility complex,mtor, mammalian target of rapamycin,mtros, mitochondrial reactive oxygen species,nadh, adenine diphosphate hydride,nf-κb, nuclear factor kappa b,nlrp3, nod-, lrr- and pyrin domain-containing 3,no, nitric oxide,oaa, oxaloacetate,oxpapc, 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphorylcholine,oxphos, oxidative phosphorylation,pamps, pathogen-associated molecular patterns,parp, poly (adp-ribose) polymerase,pge2, prostaglandin e2,phd, prolyl hydroxylases,ppar, peroxisome proliferator-activated receptor,ret, reverse electron transport,sdh, succinate dehydrogenase,sirt, sirtuin,suclg1, succinyl-coa synthetase,sucnr1, succinate receptor 1,tca, tricarboxylic acid,tlr, toll-like receptor,upr, unfolded protein response
                Biochemistry
                mitochondrial metabolism, macrophage activation, macrophage biology, mitochondrial dysfunction, oxidative stress, α-kg, α-ketoglutarate, δψm, mitochondrial membrane potential, acly, atp citrate lyase, ampk, amp-activated protein kinase, ast, aspartate aminotransferase, cic, mitochondrial citrate carrier, damps, damage-associated molecular patterns, drp1, dynamin-related protein 1, dmf, dimethyl fumarate, etc, electron transport chain, eif5a, hypusination of translation factor eukaryotic initiation factor 5a, er, endoplasmic reticulum, fao, fatty acid oxidation, fadh2, flavin adenine dinucleotide hydride, gaba, γ-amino butyric acid, gad, glutamic acid decarboxylase, gapdh, glycolytic enzyme glyceraldehyde 3-phosphate dehydrogenase, gsdmd, gasdermin d, hif-1α, hypoxia inducible factor 1α, hmgb1, high mobility group box 1, idh, isocitrate dehydrogenase, ifnγ, interferon-γ, il-4, interleukin-4, inos, inducible nitric oxide synthase, irg1, immune-responsive gene 1, klf4, krüppel-like factor 4, lps, lipopolysaccharide, mas, malate-aspartate shuttle, mdvs, mitochondria-derived vesicles, mhc, major histocompatibility complex, mtor, mammalian target of rapamycin, mtros, mitochondrial reactive oxygen species, nadh, adenine diphosphate hydride, nf-κb, nuclear factor kappa b, nlrp3, nod-, lrr- and pyrin domain-containing 3, no, nitric oxide, oaa, oxaloacetate, oxpapc, 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphorylcholine, oxphos, oxidative phosphorylation, pamps, pathogen-associated molecular patterns, parp, poly (adp-ribose) polymerase, pge2, prostaglandin e2, phd, prolyl hydroxylases, ppar, peroxisome proliferator-activated receptor, ret, reverse electron transport, sdh, succinate dehydrogenase, sirt, sirtuin, suclg1, succinyl-coa synthetase, sucnr1, succinate receptor 1, tca, tricarboxylic acid, tlr, toll-like receptor, upr, unfolded protein response

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