The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“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]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“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]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
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
Cited by
Sorted by citations
Items 201–300 of 486
Fa(c)t checking: How fatty acids shape metabolism and function of macrophages and dendritic cells
Almeida, L., & Everts, B. (2021) · European Journal of Immunology · doi:10.1002/eji.202048944 · Cited by 24
Wu, M., Zhao, Y., Tao, M., Fu, M., Wang, Y., Liu, Q., Lu, Z., & Guo, J. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c09394 · Cited by 24
Zhang, J., Liu, S., Ding, W. B., Wan, J., Qin, J., & Wang, M. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102352 · Cited by 23
Steroid hormone regulation of immunometabolism and inflammation
Smith, L. C., Ramar, M., Riley, G., Mathias, C. B., & Lee, J.-Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1654034 · Cited by 28
Intestinal Metabolites Influence Macrophage Phagocytosis and Clearance of Bacterial Infection
O’Callaghan, A. A., Dempsey, E., Iyer, N. R., Stiegeler, S., Mercurio, K., & Corr, S. C. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.622491 · Cited by 21
Apoptotic cell-derived metabolites in efferocytosis-mediated resolution of inflammation
Mao, Y. (2021) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2021.10.002 · Cited by 21
Bioenergetic Failure Drives Functional Exhaustion of Monocytes in Acute-on-Chronic Liver Failure
Maheshwari, D., Kumar, D., Jagdish, R. K., Nautiyal, N., Hidam, A. K., Kumari, R., Sehgal, R., Trehanpati, N., Baweja, S., Kumar, G., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.856587 · Cited by 21
Koenis, D. S., Matteis, R. D., Rajeeve, V., Cutillas, P. R., & Dalli, J. (2023) · Advanced Science · doi:10.1002/advs.202304690 · Cited by 19
Efferocytosis and Its Role in Rheumatic Diseases
Tang, X., Peng, Y., Jiang, Z., Yu, B., Peng, D., Xie, X., Li, F., & Ge, Y. L. (2025) · Arthritis & Rheumatology · doi:10.1002/art.43268 · Cited by 21
Pistorius, K., Ly, L., Souza, P. R., Gómez, E. A., Koenis, D. S., Rodrı́guez, A. R., Foster, J., Sosabowski, J. K., Hopkinson, M., Rajeeve, V., et al. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.103974 · Cited by 20
Mylvaganam, S., & Freeman, S. A. (2023) · Immunological Reviews · doi:10.1111/imr.13260 · Cited by 23
Pan, Y., Cao, S., Wang, Y., Tang, J., Niu, A., Kar, S. A., Jiang, M., Peng, F., Siew, G. M., Lu, W., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59393-y · Cited by 19
Immuno-metabolic interfaces in cardiac disease and failure
Bertero, E., Dudek, J., Cochain, C., Delgobo, M., Ramos, G. C., Gerull, B., Higuchi, T., Vaeth, M., Zernecke, A., Frantz, S., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab036 · Cited by 19
Huang, Q., Weng, D., Yao, S., Shen, H., Gao, S., Zhang, Y., Huang, W., Wang, Y., Wang, H., & Xu, W. (2023) · Immunity Inflammation and Disease · doi:10.1002/iid3.779 · Cited by 19
Metabolic reprogramming in efferocytosis
Yan, Q., Li, K., Chen, L., Wang, A., Xi, Y., Xiao, H., & Yuan, L. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1677028 · Cited by 19
Chen, G., Phan, V., Luo, X., & Cao, D. J. (2021) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2021.06.004 · Cited by 17
Tajbakhsh, A., Hayat, S. M. G., Karami, N., Savardashtaki, A., Butler, A. E., Rizzo, M., & Sahebkar, A. (2022) · Obesity Reviews · doi:10.1111/obr.13487 · Cited by 19
Ghost messages: cell death signals spread
Zhang, M., Lin, Y., Chen, R., Yu, H., Li, Y., Chen, M., Dou, C., Yin, P., Zhang, L., & Tang, P. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-022-01004-0 · Cited by 18
The Role of Innate Immune Cells in Cardiac Injury and Repair: A Metabolic Perspective
Banerjee, D., Tian, R., & Cai, S. (2023) · Current Cardiology Reports · doi:10.1007/s11886-023-01897-4 · Cited by 17
Metabolic regulation of macrophage proliferation and function in atherosclerosis
Patterson, M. T., & Williams, J. W. (2021) · Current Opinion in Lipidology · doi:10.1097/mol.0000000000000778 · Cited by 20
Cao, C., Liu, W., Guo, X., Weng, S., Chen, Y., Luo, Y., Wang, S., Zhu, B., Liu, Y., & Peng, D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460431 · Cited by 16
Role of macrophage polarization in heart failure and traditional Chinese medicine treatment
Zhu, Z., Wang, M., Lu, S., Dai, S., & Liu, J. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1434654 · Cited by 16
Macrophage-Associated Lipin-1 Promotes β-Oxidation in Response to Proresolving Stimuli
Schilke, R. M., Blackburn, C. M. R., Rao, S., Krzywanski, D. M., Finck, B. N., & Woolard, M. D. (2020) · ImmunoHorizons · doi:10.4049/immunohorizons.2000047 · Cited by 16
Efferocytosis: Current status and future prospects in the treatment of autoimmune diseases
Li, Q., Liu, H., Yin, G., & Xie, Q. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28399 · Cited by 17
Phenotypic and Functional Heterogeneity of Monocyte Subsets in Chronic Heart Failure Patients
Mongirdienė, A., & Liobikas, J. (2022) · Biology · doi:10.3390/biology11020195 · Cited by 15
Grid Efferocytosis via Near‐Field Electrostatic Printing Rectifies Skin Immunity
Li, M., Li, X., Wang, J., Xia, W., Bao, L., Huang, X., Mao, J., Zhao, Y., Li, Q., Cui, W., et al. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202402713 · Cited by 15
DeBerge, M., Glinton, K. E., Lantz, C. W., Ge, Z., Sullivan, D. P., Patil, S., Lee, B. R., Thorp, M. I., Mullick, A. E., Yeh, S. T., et al. (2025) · Nature Cardiovascular Research · doi:10.1038/s44161-024-00585-y · Cited by 15
Self-citationLiu, H., Huang, M., Lyu, J., Tao, J., Li, Y., Li, L., Huang, Y., & Zhou, Z. (2025) · ACS Nano · doi:10.1021/acsnano.4c13533 · Cited by 18
Intercellular communication after myocardial infarction: Macrophage as the centerpiece
Li, A., Guo, K.-Z., Yu, L.-R., Ge, J., Zhou, W., & Zhang, J.-P. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102757 · Cited by 17
Macrophage Efferocytosis as a Therapeutic Strategy in Intervertebral Disc Degeneration
Chen, S., Zhang, H., Wang, Z., Zhu, D., Li, Y., Zhang, Y., Wang, D., Chen, S.-W., Liu, H., & Kang, X. (2025) · Cell Proliferation · doi:10.1111/cpr.70068 · Cited by 15
Chen, Y., Lu, F., Zhang, Z., Li, X., Zhang, R., & Zheng, T. (2025) · Virulence · doi:10.1080/21505594.2025.2573660 · Cited by 15
Wu, H., Wu, Q., Chen, L., Hua, J., Meng, L., Nakielski, P., Lu, C., Pierini, F., Xu, L., Yu, Y., et al. (2025) · Materials Today Bio · doi:10.1016/j.mtbio.2025.102430 · Cited by 15
Gwak, S.-Y., Kim, S., Park, J., Kim, S. H., Joe, Y., Lee, H., Kim, W., Muna, I. A., Na, H., Chung, H., et al. (2021) · Gut and Liver · doi:10.5009/gnl210058 · Cited by 15
Functional implications of neutrophil metabolism during ischemic tissue repair
Piccolo, E. B., Thorp, E. B., & Sumagin, R. (2022) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2022.102191 · Cited by 16
Self-citationZhao, X., Zheng, X., Wang, Y., Chen, J., Wang, X., Xia, P., Yuan, D., Liu, Y., Wang, Z., & Du, J. (2025) · International Journal of Oral Science · doi:10.1038/s41368-025-00347-x · Cited by 14
Metabolic reprogramming of macrophages in chronic obstructive pulmonary disease
Qin, Z., Liu, W., Huang, C., & Zhang, W. Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1684075 · Cited by 15
Ge, M., Guo, Z., Ruan, Z., Ma, Y., Zhang, Z., Dong, H., Shi, T., Hu, T., Lu, L., Chen, Y., et al. (2025) · Cell Biomaterials · doi:10.1016/j.celbio.2025.100276 · Cited by 15
Emerging roles of mitochondria in animal regeneration
Zhao, Y. S., Gao, C., Pan, X., & Lei, K. (2023) · Cell Regeneration · doi:10.1186/s13619-023-00158-7 · Cited by 14
Jia, L., Liao, L., Jiang, Y., Hu, X., Lu, G., Xiao, W., Gong, W., & Jia, X. (2023) · BMC Cancer · doi:10.1186/s12885-023-11519-5 · Cited by 14
Macrophage SREBP1 regulates skeletal muscle regeneration
Oishi, Y., Koike, H., Kumagami, N., Nakagawa, Y., Araki, M., Taketomi, Y., Miki, Y., Matsuda, S., Kim, H., Matsuzaka, T., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1251784 · Cited by 16
Mitochondrial metabolism regulated macrophage phenotype in myocardial infarction
Kong, Y., Zhang, Q., Wang, S., Li, R., Fu, C., & Wei, Q. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117494 · Cited by 14
Macrophage Metabolic Signaling during Ischemic Injury and Cardiac Repair
Thorp, E. B. (2021) · Immunometabolism · doi:10.20900/immunometab20210018 · Cited by 15
Self-citationPinos, I., Yu, J., Pilli, N. R., Kane, M. A., & Amengual, J. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2023.159291 · Cited by 13
Zhang, Y., Nie, R., Feng, Z.-Y., Fan, M., Shen, Z., Zhang, X., Zhang, Q., Zou, C., Zhang, J., Huang, K., et al. (2025) · Bioactive Materials · doi:10.1016/j.bioactmat.2025.05.026 · Cited by 13
Polystyrene microplastic-induced pathophysiology is driven by disruption of efferocytosis
Codo, A. C., Romero-Pichardo, J. E., Wang, Z., Aufiero, M. A., Lazarov, T., Rojas, W. S., Walker, N. S., Nair, A., Cole, R. F., Adkins, S., et al. (2026) · Immunity · doi:10.1016/j.immuni.2026.01.009 · Cited by 14
Zhao, X., Yang, T., Zheng, M., Zhao, P., An, L., Qi, Y., Yi, K.-Q., Zhang, P.-C., & Sun, D. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-022-01030-y · Cited by 13
The role of cardiac resident macrophage in cardiac aging
Li, J., Xin, Y., Wang, Z., Li, J., Li, W., & Li, H. (2023) · Aging Cell · doi:10.1111/acel.14008 · Cited by 13
Ma, Y., Zhang, Y., Liu, X., Yang, X., Guo, H., Ding, X., Ye, C., & Guo, C. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103336 · Cited by 15
The role of multiomics in revealing the mechanism of skin repair and regeneration
Shi, S., Ou, X., Long, J., Lu, X., Xu, S., & Li, G. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1497988 · Cited by 14
Immunometabolic regulation of adipose tissue resident immune cells
Davanzo, G. G., Castro, G., & Moraes‐Vieira, P. M. (2021) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2021.03.004 · Cited by 13
Efferocytosis in Health and Disease
Li, C., Yang, Y., Zhou, F., Jiang, Q., Jiang, Y., Huang, X., Zhang, Y., Ye, Z., Xu, G. X., Kao, G., et al. (2025) · MedComm · doi:10.1002/mco2.70546 · Cited by 15
Navigating immune cell immunometabolism after liver transplantation
Zhang, W., Liu, Z., & Xu, X. (2021) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2021.103227 · Cited by 12
Tang, X., Huang, Z., Wang, F., Chen, J., Qin, D., Peng, D., & Yu, B. (2023) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2023.117374 · Cited by 13
Role of sex as a biological variable in neonatal alveolar macrophages
Leek, C. C., Cantu, A., Sonti, S., Gutierrez, M. E. C., Eldredge, L. C., Sajti, E., Xu, H. N., & Lingappan, K. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103296 · Cited by 14
Lee, S. K., Kwon, J. H., Jang, J. W., Bae, S. H., Yoon, S. K., Jung, E. S., & Choi, J. Y. (2024) · Transplantation · doi:10.1097/tp.0000000000005220 · Cited by 13
ApoEVs Transfer Mitochondrial Component to Modulate Macrophages in Periodontal Regeneration
Liu, X., Lyu, Y., Yu, Y., Wang, Z., Sun, Y., Li, M., Liang, C., Tian, W., & Liao, L. (2024) · Oral Diseases · doi:10.1111/odi.15181 · Cited by 12
Death Eaters Rely on Metabolic Signaling to Wield Anti-inflammatory Responses
Pietrangelo, A., & Ouimet, M. I. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.01.010 · Cited by 12
Dissecting inflammation in the immunemetabolomic era
Ogger, P. P., & Murray, P. J. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05715-8 · Cited by 13
Kang, Y., Jin, Q., Zhou, M., Zheng, H., Li, D. R., Wang, X., Zhou, J., Wang, Y., & Lv, J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1589923 · Cited by 12
HUMANIN produced by human efferocytic macrophages promotes the resolution of inflammation
Maraux, M., Vetter, M., Zuffo, L. D., Bonnefoy, F., Wetzel, A., Varin, A., Lamarthée, B., Tassy, O., Ducloux, D., Saas, P., et al. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07909-1 · Cited by 11
Macrophage energy metabolism in cardiometabolic disease
Wong, A., Sun, Q., Latif, I. I., & Karwi, Q. G. (2024) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-024-05099-6 · Cited by 14
Schlegel, M., Cyr, Y., Newman, A. A. C., Schreyer, K. F., Durán, J. G. B., Sharma, M., Bozal, F. K., Gourvest, M., Forest, M. L., Afonso, M. S., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2412690121 · Cited by 12
Su, Y., Xu, J., Liu, P., Shu, Y., Ma, H., Cheng, Y. Y., Liu, Y., Pan, B., & Song, K. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.137845 · Cited by 11
Zhang, K., Zhang, Y., Li, Z., Chen, J., Chang, Y., Li, Y., Zeng, S., Pan, S., Pan, S., & Huang, K. (2024) · Brain Pathology · doi:10.1111/bpa.13327 · Cited by 11
Macrophage efferocytosis promotes inflammation resolution and accelerates wound healing
Gao, J., Zhu, D., Wang, J., Khan, M. I. U., Zhang, A., Wen, X., Li, Q., Jin, P., & Shen, C. (2026) · Communications Biology · doi:10.1038/s42003-026-10107-0 · Cited by 13
Quarato, E. R., Salama, N., & Calvi, L. M. (2024) · Current Osteoporosis Reports · doi:10.1007/s11914-024-00874-2 · Cited by 11
Crosstalk between efferocytic myeloid cells and T-cells and its relevance to atherosclerosis
Ngai, D., Sukka, S. R., & Tabas, I. A. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1403150 · Cited by 10
Firouzjaei, A. A., & Mohammadi‐Yeganeh, S. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1424218 · Cited by 10
Regulators of phagocytosis as pharmacologic targets for stroke treatment
Cheng, J. G., Wang, W., Xia, Y., Li, Y., Jia, J., & Xiao, G. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1122527 · Cited by 10
Myocardial Metabolic Reprogramming in HFpEF
Zhang, Z., Sun, M., Jiang, W., Yu, L., Zhang, C., & Ma, H. (2023) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-023-10433-2 · Cited by 10
Maraux, M., Gaillardet, A., Gally, A., Saas, P., & Cherrier, T. (2020) · Journal of Immunological Methods · doi:10.1016/j.jim.2020.112810 · Cited by 10
Can polarization of macrophage metabolism enhance cardiac regeneration?
Lantz, C. W., Becker, A., & Thorp, E. B. (2021) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2021.07.003 · Cited by 10
Self-citationMetabolite transporters as regulators of macrophage polarization
Cheng, J., Cai, W., Zong, S.-Y., Yu, Y., & Wei, F. (2021) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-021-02173-4 · Cited by 10
Piollet, M., Porsch, F., Rizzo, G., Kapser, F., Schulz, D. J. J., Kiss, M. G., Schlepckow, K., Morenas‐Rodríguez, E., Sen, M. O., Gropper, J., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.15.539977 · Cited by 10
A Hypoxia–Decidual Macrophage Regulatory Axis in Normal Pregnancy and Spontaneous Miscarriage
Huang, X., Lin, Z., Zheng, Z., Shi, J., Lu, K.-Y., Wang, J., Li, M., & Shao, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179710 · Cited by 9
Tian, J., Lou, Y., Li, M., Duan, Y., Liu, H., Chen, C., Qiu, Y. F., Chen, W., Pang, C., Xiong, Y., et al. (2025) · Bioactive Materials · doi:10.1016/j.bioactmat.2025.04.034 · Cited by 9
Yang, Q., Yan, J., & Yang, Q. (2026) · Clinical and Translational Medicine · doi:10.1002/ctm2.70601 · Cited by 10
Roberts, L. M., Schwarz, B. H., Speranza, E. E., Leighton, I. A., Wehrly, T. D., Best, S. M., & Bosio, C. M. (2021) · iScience · doi:10.1016/j.isci.2021.103025 · Cited by 9
Activation of inflammatory pathways in PBMCs linking type 2 diabetes in older adults without obesity
Cheng, H.-C., Tsai, S., & Liu, H. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.111779 · Cited by 9
Liu, Z., Huo, J., Dong, W., Sun, G., Li, F.-J., Zhang, Y., Qin, Z.-W., Jiang, P., & Wang, W. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.761883 · Cited by 9
Lipin-1 restrains macrophage lipid synthesis to promote inflammation resolution
Bamgbose, T. T., Schilke, R. M., Igiehon, O. O., Nkadi, E. H., Binwal, M., Custis, D., Bharrhan, S., Schwarz, B. H., Bohrnsen, E., Bosio, C. M., et al. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkae010 · Cited by 8
Schroth, S. L., Zhang, L., Jones, R., Glinton, K. E., Mani, N. L., Inui, H., Davidson, J. T., Weinberg, S. E., Chandel, N. S., Alegre, M., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci178960 · Cited by 9
Self-citationSlc7a7 licenses macrophage glutaminolysis for restorative functions in atherosclerosis
Benhmammouch, S. C., Borowczyk, C., Pierrot-Blanchet, C., Barouillet, T., Murcy, F., Dussaud, S., Blanc, M., Blériot, C., Örd, T., Habbouche, L., et al. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01354-2 · Cited by 9
Self-citationMacrophage metabolism in inflammatory heart disease: new insights and therapeutic implications
Xiang, A., Chang, A., Zhou, J., Jin, J., Zhang, X., & Wang, Q. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1664538 · Cited by 11
More Than a Cleanup Crew: The Expanding Biology of Efferocytosis
Pandit, R., Hillman, H., Williams, J. W., & Yurdagul, A. (2025) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.125.323211 · Cited by 8
Dunphy, G., Adán‐Barrientos, I., Fernández‐Delgado, I., Villarroya‐Beltri, C., Heras‐Murillo, I., Moya-Ruiz, E., Sánchez‐Álvarez, M., Jarit-Cabanillas, A., Pozo, M. Á. D., Guerra, S., et al. (2026) · Immunity · doi:10.1016/j.immuni.2025.12.010 · Cited by 10
Yu, J., Li, J., Hu, B., Huang, X., Yang, X., Liu, Y., Cai, J.-J., Yang, X., Lai, J.-M., Shen, Y., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e26791 · Cited by 9
Piccolo, E. B., Ge, Z., Filipp, M. E., Sullivan, D. P., Thorp, E. B., & Sumagin, R. (2024) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00392.2024 · Cited by 8
Self-citationThe Macrophage–Fibroblast Dipole in the Context of Cardiac Repair and Fibrosis
Psarras, S. (2024) · Biomolecules · doi:10.3390/biom14111403 · Cited by 8
CCL2 / CCR2 Signalling in Mesenchymal Stem/Progenitor Cell Recruitment and Fracture Healing in Mice
Kannan, R., Koh, A. J., Kent, R. N., Bhutada, K., Wasi, F., Wagner, L., Kozloff, K. M., Baker, B. M., Roca, H., & McCauley, L. K. (2024) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70300 · Cited by 7
Wang, A. Y. L., Aviña, A. E., Liu, Y., Chang, Y., & Kao, H. (2025) · Antioxidants · doi:10.3390/antiox14020183 · Cited by 7
Targeting Frequent Efferocytosis in Tumor Microenvironment is a New Direction for Cancer Treatment
Zhu, G., Wan, X., Wu, W., Jia, L., Yu, X., Mo, H., Wang, X., Zhou, Q., Tang, Q., & Wang, S. (2025) · Small Science · doi:10.1002/smsc.202400479 · Cited by 7
The role of efferocytosis in inflammatory bowel disease
Liu, Y., Li, Z.-Z., Han, Y., & Wang, Q. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1524058 · Cited by 7
The role of efferocytosis in ischemic stroke and insights from retinopathy
Morris, C., Sadek, M. A., Modi, P., Abdelnaem, S. E., Rusch, N. J., Shosha, E., & Fouda, A. Y. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.06.002 · Cited by 10
Ye, K., He, Y., Jian, D., Chen, Z., Sun, H., Zhang, Y., Mai, Y., Cao, X., Wu, J., Mao, Z., et al. (2025) · Journal of Controlled Release · doi:10.1016/j.jconrel.2025.114127 · Cited by 9
Anti-Atherogenic Mechanisms and Therapies
Hudson, A., Igiehon, O. O., Woolard, M. D., & Yurdagul, A. (2025) · Current Atherosclerosis Reports · doi:10.1007/s11883-025-01324-9 · Cited by 7
Bošković, M., Pauletto, M., Giantin, M., Dacasto, M., Xiccato, G., & Trocino, A. (2025) · BMC Genomics · doi:10.1186/s12864-025-11963-6 · Cited by 7
Extracorporeal Photopheresis Stimulates Tissue Repair after Transplantation
Arella, F., Schlitt, H. J., & Riquelme, P. (2025) · Transplantation Direct · doi:10.1097/txd.0000000000001812 · Cited by 8
Yin, Y., Yan, C., Pei, X., Rao, J., Wu, L., Xue, Y., Sun, H., & Sheng, Y. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1736082 · Cited by 9
Differential impact of high-salt levels in vitro and in vivo on macrophage core functions
Müller, L., Nasr, A. R., Jux, B., Makdissi, N., Trowbridge, J. W., Schmidt, S. V., Schultze, J. L., Quast, T., Schulte-Schrepping, J., Kolanus, W., et al. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09295-x · Cited by 8
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review