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Efferocytosis Fuels Requirements of Fatty Acid Oxidation and the Electron Transport Chain to Polarize Macrophages for Tissue Repair
Open accessAbstract
During wound injury, efferocytosis fills the macrophage with a metabolite load nearly equal to the phagocyte itself. A timely question pertains to how metabolic phagocytic signaling regulates the signature anti-inflammatory macrophage response. Here we report the metabolome of activated macrophages during efferocytosis to reveal an interleukin-10 (IL-10) cytokine escalation that was independent of glycolysis yet bolstered by apoptotic cell fatty acids and mitochondrial β-oxidation, the electron transport chain, and heightened coenzyme NAD+. Loss of IL-10 due to mitochondrial complex III defects was remarkably rescued by adding NAD+ precursors. This activated a SIRTUIN1 signaling cascade, largely independent of ATP, that culminated in activation of IL-10 transcription factor PBX1. Il-10 activation by the respiratory chain was also important in vivo, as efferocyte mitochondrial dysfunction led to cardiac rupture after myocardial injury. These findings highlight a new paradigm whereby macrophages leverage efferocytic metabolites and electron transport for anti-inflammatory reprogramming that culminates in organ repair.
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“Efferocytosis leads to IL-10 induction in macrophages through signaling pathways activated by apoptotic cell cargo, including fatty acids and tryptophan (30, 40).”
From Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction–associated steatohepatitis (2025) · cites this paper as [40]
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“Among the proresolving molecules known to be induced by efferocytosis is interleukin-10 (IL-10) (30, 40)”
From Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction–associated steatohepatitis (2025) · cites this paper as [40]
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Cites
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709
Cytokine-mediated regulation of CXCR4 expression in human neutrophils
Nagase, H., Miyamasu, M., Yamaguchi, M., Imanishi, M., Tsuno, N. H., Matsushima, K., Yamamoto, K., Morita, Y., & Hirai, K. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.4.711 · Cited by 4,713
Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1112 · Cited by 3,166 · cited 3×
“This approach confirmed that apoptotic cells (Annexin V+, PI−) specifically and reproducibly induced macrophages to produce the canonical antiinflammatory cytokine IL-10 (Fadok et al., 1998) (Figures 1D and 1E).”
BackgroundMethodResolution of inflammation: the beginning programs the end
Serhan, C. N., & Savill, J. (2005) · Nature Immunology · doi:10.1038/ni1276 · Cited by 2,552
Jha, A. K., Huang, S. C.-C., Sergushichev, A., Lampropoulou, V., Ivanova, Y., Loginicheva, E., Chmielewski, K., Stewart, K. M., Ashall, J., Everts, B., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.02.005 · Cited by 2,066
Chandel, N. S., McClintock, D. S., Feliciano, C. E., Wood, T. M., Melendez, J. A., Rodriguez, A. M., & Schumacker, P. T. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m001914200 · Cited by 2,000
Self-citationLampropoulou, V., Sergushichev, A., Bambousková, M., Nair, S., Vincent, E. E., Loginicheva, E., Cervantes‐Barragán, L., Ma, X., Huang, S. C., Griss, T., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.06.004 · Cited by 1,583
Palsson-McDermott, E. M., Curtis, A. M., Goel, G., Lauterbach, M. A. R., Sheedy, F. J., Gleeson, L. E., van den Bosch, M. W. M., Quinn, S. R., Domingo-Fernandez, R., Johnston, D. G. W., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2014.12.005 · Cited by 1,397
Oxidative metabolism and PGC-1β attenuate macrophage-mediated inflammation
Vats, D., Mukundan, L., Odegaard, J. I., Zhang, L., Smith, K. L., Morel, C. R., Greaves, D. R., Murray, P. J., & Chawla, A. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.05.011 · Cited by 1,369 · cited 1×
“In skeletal cells, SIRT1 controls the transcription of peroxisome proliferator-activated receptor-gamma co-acti-vator-1α (PGC-1α) (Amat et al., 2009), which separately has been linked to IL-10 induction (Morari et al., 2010) and oxidative metabolism in macrophages (Vats et al., 2006).”
BackgroundEvans, A. M., DeHaven, C. D., Barrett, T., Mitchell, M. W., & Milgram, K. E. (2009) · Analytical Chemistry · doi:10.1021/ac901536h · Cited by 1,317
Metabolic Instruction of Immunity
Buck, M. D., Sowell, R., Kaech, S. M., & Pearce, E. L. (2017) · Cell · doi:10.1016/j.cell.2017.04.004 · Cited by 1,270
α-ketoglutarate orchestrates macrophage activation through metabolic and epigenetic reprogramming
Liu, P.-S., Wang, H., Li, X., Chao, T., Teav, T., Christen, S., Di Conza, G., Cheng, W.-C., Chou, C.-H., Vavakova, M., et al. (2017) · Nature Immunology · doi:10.1038/ni.3796 · Cited by 1,264
Cell-intrinsic lysosomal lipolysis is essential for alternative activation of macrophages
Huang, S. C., Everts, B., Ivanova, Y., O’Sullivan, D., Nascimento, M., Smith, A. M., Beatty, W. L., Love-Gregory, L. D., Lam, W. Y., O’Neill, C. M., et al. (2014) · Nature Immunology · doi:10.1038/ni.2956 · Cited by 1,256
Toll-like receptor–induced changes in glycolytic metabolism regulate dendritic cell activation
Krawczyk, C. M., Holowka, T., Sun, J., Blagih, J., Amiel, E., DeBerardinis, R. J., Cross, J. R., Jung, E., Thompson, C. B., Jones, R. G., et al. (2010) · Blood · doi:10.1182/blood-2009-10-249540 · Cited by 1,246
Apoptotic cell clearance: basic biology and therapeutic potential
Poon, I. K. H., Lucas, C. D., Rossi, A. G., & Ravichandran, K. S. (2014) · Nature Reviews Immunology · doi:10.1038/nri3607 · Cited by 1,223
Anti-Inflammatory Therapy in Chronic Disease: Challenges and Opportunities
Tabas, I., & Glass, C. K. (2013) · Science · doi:10.1126/science.1230720 · Cited by 1,093
Inflammation and plaque vulnerability
Hansson, G. K., Libby, P., & Tabas, I. A. (2015) · Journal of Internal Medicine · doi:10.1111/joim.12406 · Cited by 809
Jose, P. J., Griffiths-Johnson, D. A., COLLINS, P. D., Walsh, D. T., Moqbel, R., Totty, N. F., Truong, O., Hsuan, J. J., & Williams, T. J. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.3.881 · Cited by 806
Kim, H.-S., Patel, K., Muldoon-Jacobs, K., Bisht, K. S., Aykin-Burns, N., Pennington, J. D., van der Meer, R., Nguyen, P., Savage, J., Owens, K. M., et al. (2010) · Cancer Cell · doi:10.1016/j.ccr.2009.11.023 · Cited by 785
Self-citationA-González, N., Bensinger, S. J., Hong, C., Beceiro, S., Bradley, M. N., Zelcer, N., Deniz, J. M., Ramírez, C. M., Díaz, M., Gallardo, G., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.06.018 · Cited by 703
Huang, S. C., Smith, A. M., Everts, B., Colonna, M., Pearce, E. L., Schilling, J. D., & Pearce, E. J. (2016) · Immunity · doi:10.1016/j.immuni.2016.09.016 · Cited by 686
SIRT1 Deacetylates and Positively Regulates the Nuclear Receptor LXR
Li, X., Zhang, S., Blander, G., Tse, J. G., Krieger, M., & Guarente, L. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.07.032 · Cited by 649
Self-citationThe Sedoheptulose Kinase CARKL Directs Macrophage Polarization through Control of Glucose Metabolism
Haschemi, A., Kosma, P., Gille, L., Evans, C. R., Burant, C. F., Starkl, P., Knapp, B., Haas, R., Schmid, J. A., Jandl, C., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.023 · Cited by 635
Macrophage function in tissue repair and remodeling requires IL-4 or IL-13 with apoptotic cells
Bosurgi, L., Cao, Y. G., Cabeza-Cabrerizo, M., Tucci, A., Hughes, L. D., Kong, Y., Weinstein, J. S., Licona-Limon, P., Schmid, E. T., Pelorosso, F., et al. (2017) · Science · doi:10.1126/science.aai8132 · Cited by 560
Tanner, K. G., Landry, J. W., Sternglanz, R., & Denu, J. M. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250422697 · Cited by 557
Complementation of mitochondrial electron transport chain by manipulation of the NAD + /NADH ratio
Titov, D. V., Cracan, V., Goodman, R. P., Peng, J., Grabarek, Z., & Mootha, V. K. (2016) · Science · doi:10.1126/science.aad4017 · Cited by 518
METABOLIC PATTERNS IN THREE TYPES OF PHAGOCYTIZING CELLS
Oren, R., Farnham, A. E., Saito, K., Milofsky, E. S., & Karnovsky, M. L. (1963) · The Journal of Cell Biology · doi:10.1083/jcb.17.3.487 · Cited by 504
Screening large-scale association study data: exploiting interactions using random forests
Lunetta, K. L., Hayward, B., Segal, J., & Eerdewegh, P. V. (2004) · BMC Genetics · doi:10.1186/1471-2156-5-32 · Cited by 478
Mitochondria and cell signalling
Tait, S. W. G., & Green, D. R. (2012) · Journal of Cell Science · doi:10.1242/jcs.099234 · Cited by 453
Krishnamurthy, P., Rajasingh, J., Lambers, E., Qin, G., Losordo, D. W., & Kishore, R. (2008) · Circulation Research · doi:10.1161/circresaha.108.188243 · Cited by 428
Wan, E. Y., Yeap, X. Y., Dehn, S., Terry, R. L., Novak, M. L., Zhang, S., Iwata, S., Han, X., Homma, S., Drosatos, K., et al. (2013) · Circulation Research · doi:10.1161/circresaha.113.301198 · Cited by 401
Self-citationMitochondrial fission promotes the continued clearance of apoptotic cells by macrophages
Wang, Y., Subramanian, M., Yurdagul, A., Barbosa-Lorenzi, V. C., Cai, B., de Juan-Sanz, J., Ryan, T. A., Nomura, M., Maxfield, F. R., & Tabas, I. (2017) · Cell · doi:10.1016/j.cell.2017.08.041 · Cited by 364
Etomoxir Inhibits Macrophage Polarization by Disrupting CoA Homeostasis
Divakaruni, A. S., Hsieh, W. Y., Minarrieta, L., Duong, T., Kim, K. K. O., Desousa, B. R., Andreyev, A. Y., Bowman, C. E., Caradonna, K. L., Dranka, B. P., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.06.001 · Cited by 364
Alternatively activated macrophages determine repair of the infarcted adult murine heart
Shiraishi, M., Shintani, Y., Shintani, Y., Ishida, H., Saba, R., Yamaguchi, A., Adachi, H., Yashiro, K., & Suzuki, K. (2016) · Journal of Clinical Investigation · doi:10.1172/jci85782 · Cited by 353
Varia, M. A., Calkins-Adams, D. P., Rinker, L. H., Kennedy, A. S., Novotny, D. B., Fowler, W. C., & Raleigh, J. A. (1998) · Gynecologic Oncology · doi:10.1006/gyno.1998.5163 · Cited by 346
Hartl, F. U., Schmidt, B., Wächter, E., Weiss, H., & Neupert, W. (1986) · Cell · doi:10.1016/0092-8674(86)90809-3 · Cited by 334
The mitochondrial respiratory chain is essential for haematopoietic stem cell function
Ansó, E., Weinberg, S. E., Diebold, L. P., Thompson, B. J., Malinge, S., Schumacker, P. T., Liu, X., Zhang, Y., Shao, Z., Steadman, M., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3529 · Cited by 327
Self-citationAutophagy-Dependent Generation of Free Fatty Acids Is Critical for Normal Neutrophil Differentiation
Riffelmacher, T., Clarke, A. J., Richter, F. C., Stranks, A. J., Pandey, S., Danielli, S., Hublitz, P., Yu, Z., Johnson, E., Schwerd, T., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.08.005 · Cited by 309
Yamamoto, T., Byun, J., Zhai, P., Ikeda, Y., Oka, S., & Sadoshima, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098972 · Cited by 305
Partitioning Circadian Transcription by SIRT6 Leads to Segregated Control of Cellular Metabolism
Masri, S., Rigor, P., Cervantes, M., Ceglia, N., Sebastian, C., Xiao, C., Roqueta-Rivera, M., Deng, C., Osborne, T. F., Mostoslavsky, R., et al. (2014) · Cell · doi:10.1016/j.cell.2014.06.050 · Cited by 292
CD38-NAD+Axis Regulates Immunotherapeutic Anti-Tumor T Cell Response
Chatterjee, S., Daenthanasanmak, A., Chakraborty, P., Wyatt, M. W., Dhar, P., Selvam, S. P., Fu, J., Zhang, J., Nguyen, H., Kang, I., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.10.006 · Cited by 270
Continued clearance of apoptotic cells critically depends on the phagocyte Ucp2 protein
Park, D., Han, C. Z., Elliott, M. R., Kinchen, J. M., Trampont, P. C., Das, S., Collins, S., Lysiak, J. J., Hoehn, K. L., & Ravichandran, K. S. (2011) · Nature · doi:10.1038/nature10340 · Cited by 250
Self-citationDeBerge, M., Yeap, X. Y., Dehn, S., Zhang, S., Grigoryeva, L. S., Misener, S., Procissi, D., Zhou, X., Lee, D. C., Müller, W. A., et al. (2017) · Circulation Research · doi:10.1161/circresaha.117.311327 · Cited by 250
Self-citationChung, E. Y., Liu, J., Homma, Y., Zhang, Y., Brendolan, A., Saggese, M., Han, J., Silverstein, R. L., Selleri, L., & Ma, X. (2007) · Immunity · doi:10.1016/j.immuni.2007.11.014 · Cited by 249
Amat, R., Planavila, A., Chen, S. L., Iglesias, R., Giralt, M., & Villarroya, F. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.022749 · Cited by 224
The infarcted myocardium solicits GM-CSF for the detrimental oversupply of inflammatory leukocytes
Anzai, A., Choi, J. L., He, S., Fenn, A. M., Nairz, M., Rattik, S., McAlpine, C. S., Mindur, J. E., Chan, C. T., Iwamoto, Y., et al. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20170689 · Cited by 219
Studies on the Biosynthesis of Nicotinamide Adenine Dinucleotide
Ikeda, M., Tsuji, H., Nakamura, S., Ichiyama, A., Nishizuka, Y., & Hayaishi, O. (1965) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)97589-7 · Cited by 203
Eller, K., Wolf, D. G. F., Huber, J., Metz, M., Mayer, G. J., McKenzie, A. N. J., Maurer, M., Rosenkranz, A. R., & Wolf, A. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001183 · Cited by 187
HoWangYin, K.-Y., Zlatanova, I., Pinto, C., Ngkelo, A., Cochain, C., Rouanet, M., Vilar, J., Lemitre, M., Stockmann, C., Fleischmann, B. K., et al. (2016) · Circulation · doi:10.1161/circulationaha.115.020857 · Cited by 173
Wang, Y., Mohsen, A.-W. A., Mihalik, S. J., Goetzman, E. S., & Vockley, J. E. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.139493 · Cited by 169
Macrophage-derived IL-10 mediates mucosal repair by epithelial WISP-1 signaling.
Quirós, M., Nishio, H., Neumann, P., Siuda, D., Brazil, J., Azcutia, V., Hilgarth, R., O'Leary, M. N., Garcia-Hernandez, V., Leoni, G., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci90229 · Cited by 169
Efficient Phagocytosis Requires Triacylglycerol Hydrolysis by Adipose Triglyceride Lipase
Chandak, P. G., Radović, B., Aflaki, E., Kolb, D., Buchebner, M., Fröhlich, E., Magnes, C., Sinner, F., Haemmerle, G., Zechner, R., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.107854 · Cited by 163
Inhibition of NADP dependent oxidoreductases by the 6‐aminonicotinamide analogue of NADP
Köhler, E., Barrach, H.-J., & Neubert, D. (1970) · FEBS Letters · doi:10.1016/0014-5793(70)80063-1 · Cited by 162
Waypa, G. B., Marks, J. D., Guzy, R. D., Mungai, P. T., Schriewer, J. M., Đokić, D., Ball, M. K., & Schumacker, P. T. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201207-1294oc · Cited by 154
Self-citationModification of the fatty acid composition of cultured human fibroblasts.
Spector, A. A., Kiser, R. E., Denning, G. M., Koh, S. W., & DeBault, L. E. (1979) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)40609-1 · Cited by 138
Transcriptional and Translational Regulation of TGF-β Production in Response to Apoptotic Cells
Xiao, Y. Q., Freire-de-Lima, C. G., Schiemann, W. P., Bratton, D. L., Vandivier, R. W., & Henson, P. M. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.5.3575 · Cited by 131
Alvey, C. M., Spinler, K. R., Irianto, J., Pfeifer, C. R., Hayes, B. H., Xia, Y., Cho, S., Dingal, P. C. D. P., Hsu, J., Smith, L., et al. (2017) · Current Biology · doi:10.1016/j.cub.2017.06.005 · Cited by 116
Schönfeld, P., Wieckowski, M. R., Lebiedzińska, M., & Wojtczak, L. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.01.010 · Cited by 102
Dehn, S., & Thorp, E. B. (2017) · The FASEB Journal · doi:10.1096/fj.201700450r · Cited by 68
Self-citationCiarlo, E., Heinonen, T., Théroude, C., Herderschee, J., Mombelli, M., Lugrin, J., Pfefferlé, M., Tyrrell, B. E., Lensch, S., Acha‐Orbea, H., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01037 · Cited by 61
Biochemical and physiologic consequences of carnitine palmityltransferase deficiency
Carroll, J. E., Brooke, M. H., Vivo, D. C. D., Kaiser, K. K., & Hagberg, J. M. (1978) · Muscle & Nerve · doi:10.1002/mus.880010203 · Cited by 55
NAMPT-Mediated Salvage Synthesis of NAD+ Controls Morphofunctional Changes of Macrophages
Venter, G., Oerlemans, F. T. J. J., Willemse, M. P., Wijers, M., Fransen, J. A. M., & Wieringa, B. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097378 · Cited by 51
Cardiomyocytes induce macrophage receptor shedding to suppress phagocytosis
Zhang, S., Yeap, X., Grigoryeva, L. S., Dehn, S., DeBerge, M., Tye, M. Y., Rostlund, E., Schrijvers, D. M., Zhang, Z. J., Sumagin, R., et al. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.08.009 · Cited by 40
Self-citationElectron transfer through the isolated mitochondrial cytochrome b-c1 complex
Rich, P. R. (1983) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(83)90073-7 · Cited by 37
Morari, J., Torsoni, A. S., Anhê, G. F., Roman, E. A., Cintra, D. E., Ward, L. S., Bordin, S. A., & Velloso, L. A. (2009) · Metabolism · doi:10.1016/j.metabol.2009.07.020 · Cited by 19
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Metadata
- Authors
- Zhang, S., Weinberg, S., DeBerge, M., Gainullina, A., Schipma, M., Kinchen, J. M., Ben-Sahra, I., Gius, D. R., Yvan-Charvet, L., Chandel, N. S., Schumacker, P. T., & Thorp, E. B.
- Affiliations
- Northwestern University (US)
- ITMO University (RU)
- Metabolon (United States) (US)
- Corresponding author
- Thorp, Edward B.
- ORCID
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2019-02
- Volume
- 29
- Issue
- 2
- Pages
- 443-456.e5
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC6471613
- OpenAlex
- W2907223756
- Cited by
- 485
- References
- 65
- Citations by year
- 2026: 82 · 2025: 90 · 2024: 84 · 2023: 71 · 2022: 45 · 2021: 62 · 2020: 31 · 2019: 20
- FWCI
- 12.06
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NHLBI (F32HL127958, HL122309, HL139812)
- Chicago Biomedical Consortium
- Sidney Bess Memorial Fund (2R01CA152601-A1, 1R01CA152799-01A1, 1R01CA168292-01A1, 1R01CA214025-01)
- Avon Foundation
- Lynn Sage Cancer Research Foundation
- Chicago Community Trust
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Keywords
- efferocytosis, macrophage polarization, IL-10, mitochondrial beta-oxidation, electron transport chain, NAD+, SIRT1, PBX1, mitochondrial complex III, wound healing, myocardial injury, cardiac rupture, anti-inflammatory macrophages, tissue repair
- MeSH terms
- Animals, Electron Transport, Fatty Acids, Humans, Inflammation, Macrophages, Mice, Inbred C57BL, Mitochondria, NAD, Oxidation-Reduction, Wound Healing, Interleukin-10, Jurkat Cells, Mice, Cytophagocytosis
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