The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
TLR-driven early glycolytic reprogramming via the kinases TBK1-IKKɛ supports the anabolic demands of dendritic cell activation
Open accessAbstract
The ligation of Toll-like receptors (TLRs) leads to rapid activation of dendritic cells (DCs). However, the metabolic requirements that support this process remain poorly defined. We found that DC glycolytic flux increased within minutes of exposure to TLR agonists and that this served an essential role in supporting the de novo synthesis of fatty acids for the expansion of the endoplasmic reticulum and Golgi required for the production and secretion of proteins that are integral to DC activation. Signaling via the kinases TBK1, IKKɛ and Akt was essential for the TLR-induced increase in glycolysis by promoting the association of the glycolytic enzyme HK-II with mitochondria. In summary, we identified the rapid induction of glycolysis as an integral component of TLR signaling that is essential for the anabolic demands of the activation and function of DCs.
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?
In the citing paper
“The increased degradation of key enzymes, such as SUCLA2, ALDH2 and ACO2, is consistent with a reported shift in LPS-stimulated DCs from oxidative phosphorylation and oxygen consumption to glycolysis, glucose consumption and lactate production (39–42).”
From Dynamic profiling of the protein life cycle in response to pathogens (2015) · cites this paper as [42]
In the citing paper
“Metabolic state is directly manipulated by cytokine and pattern-recognition receptors, and elevated glycolytic activity has been tied to immune cell activation (Everts et al., 2014; O’Neill and Pearce, 2016).”
From Complex cell-state changes revealed by single cell RNA sequencing of 76,149 microglia throughout the mouse lifespan and in the injured brain (2018) · cites this paper as Everts et al., 2014
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
1 retracted
Guo, J., Coppola, D., & Cheng, J. Q. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.287433 · Cited by 87
RetractedSuccinate is an inflammatory signal that induces IL-1β through HIF-1α
Tannahill, G. M., Curtis, A. M., Adamik, J., Palsson-McDermott, E. M., McGettrick, A. F., Goel, G., Frezza, C., Bernard, N. J., Kelly, B., Foley, N. H., et al. (2013) · Nature · doi:10.1038/nature11986 · Cited by 4,176
Lutz, M. B., Kukutsch, N. A., Ogilvie, A. L. J., Rößner, S., Koch, F., Romani, N., & Schuler, G. (1999) · Journal of Immunological Methods · doi:10.1016/s0022-1759(98)00204-x · Cited by 2,972
Assessing mitochondrial dysfunction in cells
Brand, M. D., & Nicholls, D. G. (2011) · Biochemical Journal · doi:10.1042/bj20110162 · Cited by 2,436
Posttranscriptional Control of T Cell Effector Function by Aerobic Glycolysis
Chang, C.-H., Curtis, J. D., Maggi, L. B., Faubert, B., Villarino, A. V., O’Sullivan, D., Huang, S. C.-C., van der Windt, G. J. W., Blagih, J., Qiu, J., et al. (2013) · Cell · doi:10.1016/j.cell.2013.05.016 · Cited by 2,204
Self-citationMetabolic Pathways in Immune Cell Activation and Quiescence
Pearce, E. L., & Pearce, E. J. (2013) · Immunity · doi:10.1016/j.immuni.2013.04.005 · Cited by 1,692
Self-citationEnhancing CD8 T-cell memory by modulating fatty acid metabolism
Pearce, E. L., Walsh, M. C., Cejas, P. J., Harms, G. M., Shen, H., Wang, L.-S., Jones, R. G., & Choi, Y. (2009) · Nature · doi:10.1038/nature08097 · Cited by 1,559
Self-citationMitochondrial respiratory capacity is a critical regulator of CD8+ T cell memory development
van der Windt, G. J. W., Everts, B., Chang, C.-H., Curtis, J. D., Freitas, T. C., Amiel, E., Pearce, E. J., & Pearce, E. L. (2012) · Immunity · doi:10.1016/j.immuni.2011.12.007 · Cited by 1,540
Self-citationToll-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
Self-citationCleeter, M. W. J., Cooper, J. M., Darley-Usmar, V. M., Moncada, S., & Schapira, A. H. V. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00424-2 · Cited by 1,241
Cited by
Sorted by citations
Items 301–400 of 999
Strategies to Improve the Efficacy of Dendritic Cell-Based Immunotherapy for Melanoma
Hargadon, K. M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01594 · Cited by 69
Merkley, S. D., Chock, C. J., Yang, X. O., Harris, J., & Castillo, E. F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02914 · Cited by 68
Snyder, J. P., & Amiel, E. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03145 · Cited by 68
Self-citationChaudhary, V., Kioon, M. D. A., Hwang, S., Mishra, B., Lakin, K. S., Kirou, K. A., Zhang-Sun, J., Wiseman, R. L., Spiera, R., Crow, M. K., et al. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20221085 · Cited by 69
Caslin, H. L., Taruselli, M. T., Haque, T. T., Pondicherry, N., Baldwin, E. A., Barnstein, B. O., & Ryan, J. J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.03026 · Cited by 70
Calì, C., Cantando, I., Veloz Castillo, M. F., Gonzalez, L., & Bezzi, P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168922 · Cited by 66
Lipid homeostasis in diabetic kidney disease
Wang, Y., Liu, T., Wu, Y., Wang, L., Ding, S., Hou, B., Zhao, H., Liu, W., & Li, P. (2024) · International Journal of Biological Sciences · doi:10.7150/ijbs.95216 · Cited by 75
TANK-Binding Kinase 1-Dependent Responses in Health and Autoimmunity
Louis, C., Burns, C. J., & Wicks, I. P. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00434 · Cited by 64
Metabolic regulation of inflammasomes in inflammation
Yang, Q., Liu, R., Yu, Q., Bi, Y., & Liu, G. (2019) · Immunology · doi:10.1111/imm.13056 · Cited by 68
Interactions between gut microbes and NLRP3 inflammasome in the gut-brain axis
Ding, Y., Wang, Z., Chen, Y., Guo, Q., & Dong, Y. (2023) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2023.03.017 · Cited by 69
Dual Proteolytic Pathways Govern Glycolysis and Immune Competence
Lü, W., Zhang, Y., McDonald, D., Jing, H., Carroll, B., Robertson, N., Zhang, Q., Griffin, H. R., Sanderson, S., Lakey, J. H., et al. (2014) · Cell · doi:10.1016/j.cell.2014.12.001 · Cited by 68
LKB1 orchestrates dendritic cell metabolic quiescence and anti-tumor immunity
Wang, Y., Du, X., Wei, J., Long, L., Tan, H., Guy, C. S., Dhungana, Y., Qian, C., Neale, G. A. M., Fu, Y., et al. (2019) · Cell Research · doi:10.1038/s41422-019-0157-4 · Cited by 65
Role of PKM2-Mediated Immunometabolic Reprogramming on Development of Cytokine Storm
Liu, Z., Le, Y., Chen, H., Zhu, J., & Lu, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.748573 · Cited by 66
Metabolism and acetylation in innate immune cell function and fate
Cameron, A. M., Lawless, S. J., & Pearce, E. J. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.10.003 · Cited by 65
Self-citationZahoor, I., Suhail, H., Datta, I., Ahmed, M. E., Poisson, L., Waters, J., Rashid, F., Rui, B., Singh, J., Cerghet, M., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2123265119 · Cited by 62
Enhanced glycolysis contributes to the pathogenesis of experimental autoimmune neuritis
Liu, R.-T., Zhang, M., Yang, C.-L., Zhang, P., Zhang, N., Du, T., Ge, M., Yue, L.-T., Li, X., Li, H., et al. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1095-7 · Cited by 62
Regulation of fatty acid synthesis in immune cells
Qian, X., Yang, Z., Mao, E., & Chen, E. (2018) · Scandinavian Journal of Immunology · doi:10.1111/sji.12713 · Cited by 65
Gu, R., Zhang, F., Chen, G., Han, C., Liu, J., Ren, Z., Zhu, Y., Waddington, J. L., Zheng, L. T., & Zhen, X. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.10.018 · Cited by 62
Bakker, N. V. T., & Pearce, E. J. (2020) · Immunological Reviews · doi:10.1111/imr.12848 · Cited by 62
Self-citationRole of Dendritic Cells in the Induction of Lymphocyte Tolerance
Osorio, F., Fuentes, C., López, M. N., Salazar‐Onfray, F., & González, F. E. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00535 · Cited by 64
Metabolic reprogramming: an innate cellular defence mechanism against intracellular bacteria?
Escoll, P., & Buchrieser, C. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.05.009 · Cited by 61
Superoxide Dismutase 1 Protects Hepatocytes from Type I Interferon-Driven Oxidative Damage
Bhattacharya, A., Hegazy, A. N., Deigendesch, N., Kosack, L., Cupovic, J., Kandasamy, R. K., Hildebrandt, A., Merkler, D., Kühl, A. A., Vilagos, B., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.10.013 · Cited by 60
Tricarboxylic acid cycle metabolites in the control of macrophage activation and effector phenotypes
Noe, J. T., & Mitchell, R. A. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ru1218-496r · Cited by 63
Hargadon, K. M. (2020) · Clinical and Translational Medicine · doi:10.1002/ctm2.37 · Cited by 63
Carbohydrate and Amino Acid Metabolism as Hallmarks for Innate Immune Cell Activation and Function
Zhao, H., Raines, L. N., & Huang, S. C. (2020) · Cells · doi:10.3390/cells9030562 · Cited by 62
Self-citationPyruvate Kinase M2 Promotes the Activation of Dendritic Cells by Enhancing IL-12p35 Expression
Jin, X., Zhang, W., Wang, Y., Liu, J., Hao, F., Li, Y., Tian, M., Shu, H., Dong, J., Feng, Y., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107690 · Cited by 61
Kamyshnyi, O., Matskevych, V. M., Lenchuk, T., Strilbytska, O. M., Storey, K. B., & Lushchak, O. V. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112230 · Cited by 62
Glycolysis in Innate Immune Cells Contributes to Autoimmunity
Xu, Y., Chen, Y., Zhang, X., Ma, J., Liu, Y., Cui, L., & Wang, F. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.920029 · Cited by 64
Menn, G. L., & Neels, J. G. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061575 · Cited by 61
Immunometabolism: new insights and lessons from antigen-directed cellular immune responses
Ramalho, R., Rao, M., Zhang, C., Agrati, C., Ippolito, G., Wang, F., Zumla, A. I., & Maeurer, M. J. (2020) · Seminars in Immunopathology · doi:10.1007/s00281-020-00798-w · Cited by 63
Cui, H., Banerjee, S., Guo, S., Xie, N., & Liu, G. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701571 · Cited by 56
Metabolic Alterations in SARS-CoV-2 Infection and Its Implication in Kidney Dysfunction
Andrade-Silva, M., da Silva, A. R. P. A., do Amaral, M. A., de Fragas, M. G., & Câmara, N. O. S. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.624698 · Cited by 60
Targeting citrate as a novel therapeutic strategy in cancer treatment
Huang, L., Wang, C., Xu, H., & Peng, G. (2019) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2019.188332 · Cited by 60
High fructose-induced metabolic changes enhance inflammation in human dendritic cells
Jaiswal, N., Agrawal, S., & Agrawal, A. (2019) · Clinical & Experimental Immunology · doi:10.1111/cei.13299 · Cited by 61
Kotlyarov, S. N., & Котлярова, А. А. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312803 · Cited by 59
Sen, K., Pati, R., Jha, A., Mishra, G. P., Prusty, S., Chaudhary, S., Swetalika, S., Podder, S., Sen, A., Swain, M., et al. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102575 · Cited by 57
Metabolic regulation of dendritic cell activation and immune function during inflammation
Wu, L., Yan, Z., Jiang, Y., Chen, Y., Du, J., Guo, L., Xu, J., Luo, Z., & Liu, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1140749 · Cited by 62
Immunometabolism of tumor-associated macrophages: A therapeutic perspective
Karimova, A. F., Khalitova, A. R., Suezov, R. V., Markov, N., Mukhamedshina, Y. O., Rizvanov, A. A., Huber, M., Simon, H., & Brichkina, A. I. (2025) · European Journal of Cancer · doi:10.1016/j.ejca.2025.115332 · Cited by 65
Hansen, I. S., Krabbendam, L., Bernink, J. H., Loayza‐Puch, F., Hoepel, W., van Burgsteden, J. A., Kuijper, E. C., Buskens, C. J., Bemelman, W. A., Zaat, S. A. J., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03318-5 · Cited by 58
Self-citationChrisikos, T. T., Zhou, Y., Slone, N., Babcock, R. L., Watowich, S. S., & Li, H. S. (2018) · Molecular Immunology · doi:10.1016/j.molimm.2018.01.014 · Cited by 61
miR-142 controls metabolic reprogramming that regulates dendritic cell activation
Sun, Y., Oravecz-Wilson, K. I., Bridges, S., McEachin, R. C., Wu, J. J., Kim, S. H., Taylor, A., Zajac, C. K., Fujiwara, H., Peltier, D., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci123839 · Cited by 58
IL-1 induces mitochondrial translocation of IRAK2 to suppress oxidative metabolism in adipocytes
Zhou, H., Wang, H., Yu, M., Schugar, R. C., Qian, W., Tang, F., Liu, W., Yang, H., McDowell, R. E., Zhao, J., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0750-1 · Cited by 58
Targeting immunometabolism in host defence against Mycobacterium tuberculosis
Sheedy, F. J., & Divangahi, M. (2020) · Immunology · doi:10.1111/imm.13276 · Cited by 62
Diversity and environmental adaptation of phagocytic cell metabolism
Davies, L. C., Rice, C. M., McVicar, D. W., & Weiss, J. M. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.4ri0518-195r · Cited by 56
New Roles for Glycogen in Tumor Progression
Dauer, P., & Lengyel, E. R. (2019) · Trends in cancer · doi:10.1016/j.trecan.2019.05.003 · Cited by 57
The Importance of Metabolism for Immune Homeostasis in Allergic Diseases
Rodríguez‐Coira, J., Villaseñor, A., Izquierdo, E., Huang, M., Barker‐Tejeda, T. C., Radzikowska, U., Sokołowska, M., & Barber, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.692004 · Cited by 58
Mitochondrial respiration contributes to the interferon gamma response in antigen-presenting cells
Kiritsy, M. C., McCann, K. J., Mott, D., Holland, S. M., Behar, S. M., Sassetti, C. M., & Olive, A. J. (2021) · eLife · doi:10.7554/elife.65109 · Cited by 58
Kim, H., & Shin, S. J. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.891878 · Cited by 60
Immunometabolism at the Heart of Cardiovascular Disease
DeBerge, M., Chaudhary, R. K., Schroth, S. L., & Thorp, E. B. (2023) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2022.12.010 · Cited by 59
The metabolic axis of macrophage and immune cell polarization
Hobson-Gutierrez, S., & Carmona‐Fontaine, C. (2018) · Disease Models & Mechanisms · doi:10.1242/dmm.034462 · Cited by 57
Tolerogenic Dendritic Cells: The Pearl of Immunotherapy in Organ Transplantation
Zhuang, Q., Cai, H., Cao, Q., Li, Z., Liu, S., & Ming, Y. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.552988 · Cited by 58
Wassie, T., Lu, Z., Duan, X., Xie, C., Gebeyew, K., Yumei, Z., Yin, Y., & Wu, X. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.783819 · Cited by 57
Dendritic cells in sepsis: Potential immunoregulatory cells with therapeutic potential
Kumar, V. (2018) · Molecular Immunology · doi:10.1016/j.molimm.2018.07.007 · Cited by 57
Metabolism of Innate Immune Cells in Cancer
Talty, R., & Olino, K. L. (2021) · Cancers · doi:10.3390/cancers13040904 · Cited by 55
Basic mechanism of immune system activation by mitochondria
Iwasaki, Y., Takeshima, Y., & Fujio, K. (2020) · Immunological Medicine · doi:10.1080/25785826.2020.1756609 · Cited by 53
Volpedo, G., Pacheco‐Fernández, T., Bhattacharya, P., Oljuskin, T., Dey, R., Gannavaram, S., Satoskar, A. R., & Nakhasi, H. L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.748325 · Cited by 57
Trained Immunity Contribution to Autoimmune and Inflammatory Disorders
Funes, S. C., Ríos, M., Fernández‐Fierro, A., Genaro, M. S. D., & Kalergis, A. M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.868343 · Cited by 53
The bioenergetics of inflammation: insights into obesity and type 2 diabetes
Keane, K. N., Calton, E. K., Carlessi, R., Hart, P. H., & Newsholme, P. (2017) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2017.45 · Cited by 54
Consiglio, C. R., Udartseva, O. O., Ramsey, K. D., Bush, C., & Gollnick, S. O. (2020) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-19-0371 · Cited by 52
Emerging Roles of Cellular Metabolism in Regulating Dendritic Cell Subsets and Function
Du, X., Chapman, N. M., & Chi, H. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00152 · Cited by 51
Molecular Aspects of Dendritic Cell Activation in Leishmaniasis: An Immunobiological View
Tibúrcio, R., Nunes, S., Nunes, I. V., Ampuero, M. R., Bonyek-Silva, Í., Lima, R., Tavares, N. M., & Brodskyn, C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00227 · Cited by 53
Sun, C., Liang, H., Zhao, Y., Li, S., Li, X., Yuan, X., Cheng, G., Zhang, Y., Liu, M., Guan, Y., et al. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115913 · Cited by 52
Neonatal monocytes exhibit a unique histone modification landscape
Bermick, J., Lambrecht, N., denDekker, A. D., Kunkel, S. L., Lukacs, N. W., Hogaboam, C. M., & Schaller, M. A. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0265-7 · Cited by 52
Campbell, N. K., Fitzgerald, H. K., Fletcher, J. M., & Dunne, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00345 · Cited by 52
Pulmonary Pathogens Adapt to Immune Signaling Metabolites in the Airway
Riquelme, S. A., Lung, T. W. F., & Prince, A. S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00385 · Cited by 53
Depletion and Dysfunction of Dendritic Cells: Understanding SARS-CoV-2 Infection
Chang, T., Yang, J., Deng, H., Chen, D., Yang, X., & Tang, Z. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.843342 · Cited by 57
Metformin attenuated sepsis-associated liver injury and inflammatory response in aged mice
Song, H., Zhang, X., Zhai, R., Liang, H., Song, G., Yuan, Y., Xu, Y., Yan, Y., Qiu, L., & Sun, T. (2022) · Bioengineered · doi:10.1080/21655979.2022.2036305 · Cited by 52
Dooming Phagocyte Responses: Inflammatory Effects of Endogenous Oxidized Phospholipids
Gioia, M. D., & Zanoni, I. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.626842 · Cited by 53
Fatty Acid Metabolism and Cancer Immunotherapy
Luo, Y., Wang, H., Liu, B., & Wei, J. (2022) · Current Oncology Reports · doi:10.1007/s11912-022-01223-1 · Cited by 53
Li, Y., Zhou, H., He, X., Jin, L., Zhu, Y., Hu, L., Feng, M.-J., Zhu, J., Wang, L., Zheng, Y., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.08.016 · Cited by 52
Endoplasmic Reticulum Stress Sensor IRE1α Enhances IL-23 Expression by Human Dendritic Cells
Márquez, S., Fernández, J. J., Terán-Cabanillas, E., Herrero-Sánchez, C., Alonso, S., Azogil, A., Montero, O., Iwawaki, T., Cubillos‐Ruiz, J. R., Fernández, N., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00639 · Cited by 53
Immunometabolism: A new target for improving cancer immunotherapy
Guo, C., Chen, S., Liu, W., Ma, Y., Li, J., Fisher, P. B., Fang, X., & Wang, X. (2019) · Advances in cancer research · doi:10.1016/bs.acr.2019.03.004 · Cited by 56
Liu, J., Cui, Y., Cabral, H., Tong, A., Yue, Q., Zhao, L., Sun, X., & Mi, P. (2024) · ACS Nano · doi:10.1021/acsnano.4c09053 · Cited by 51
Hussaarts, L., Yazdanbakhsh, M., & Guigas, B. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00499 · Cited by 48
Immunometabolism in the Tumor Microenvironment
Roy, D. G., Kaymak, I., Williams, K. S., Ma, E. H., & Jones, R. G. (2020) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-030518-055817 · Cited by 49
Self-citationJeske, R., Yuan, X., Fu, Q., Bunnell, B. A., Logan, T. M., & Li, Y. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.621744 · Cited by 49
Li, D. X., Yang, S., Xing, Y., Pan, L., Zhao, R., Zhao, Y., Liu, L., & Wu, M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.673839 · Cited by 50
Wang, R., Zhuang, J., Zhang, Q., Wu, W., Yu, X., Zhang, H., & Xie, Z. (2025) · Experimental Hematology and Oncology · doi:10.1186/s40164-025-00689-6 · Cited by 52
Lipid metabolism in homeostasis and disease
Li, Z., Deng, W., Yang, L., Tang, C., Yue, J.-M., Monteiro, O., Baptista‐Hon, D. T., & Li, T. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02357-x · Cited by 58
Vacaflores, A., Chapman, N. M., Harty, J. T., Richer, M. J., & Houtman, J. C. D. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157175 · Cited by 48
Newling, M., Sritharan, L., van der Ham, A. J., Hoepel, W., Fiechter, R. H., de Boer, L., Zaat, S. A. J., Bisoendial, R. J., Baeten, D., Everts, B., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900172 · Cited by 52
Self-citationImmunometabolism, pregnancy, and nutrition
Thiele, K., Diao, L., & Arck, P. (2017) · Seminars in Immunopathology · doi:10.1007/s00281-017-0660-y · Cited by 48
Cancer, obesity and immunometabolism – Connecting the dots
Dyck, L., & Lynch, L. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.12.019 · Cited by 48
Stüve, P., Minarrieta, L., Erdmann, H., Arnold‐Schrauf, C., Swallow, M., Guderian, M., Krull, F., Hölscher, A., Ghorbani, P., Behrends, J., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00495 · Cited by 52
Regulation of leukocyte function by citric acid cycle intermediates
Patil, N. K., Bohannon, J. K., Hernandez, A., Patil, T. K., & Sherwood, E. R. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mir1118-415r · Cited by 49
Pelgrom, L. R., Patente, T. A., Sergushichev, A., Esaulova, E., Otto, F., Ozir‐Fazalalikhan, A., van der Zande, H. J. P., van der Ham, A. J., van der Stel, S. D., Artyomov, M. N., et al. (2019) · Cell Research · doi:10.1038/s41422-019-0161-8 · Cited by 48
Self-citationShaping of Dendritic Cell Function by the Metabolic Micro-Environment
Brombacher, E. C., & Everts, B. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00555 · Cited by 45
Self-citationExtracellular Matrix Injury of Kidney Allografts in Antibody-Mediated Rejection: A Proteomics Study
Clotet‐Freixas, S., McEvoy, C. M., Batruch, I., Pastrello, C., Kotlyar, M., Van, J. A. D., Arambewela, M., Boshart, A., Farkona, S., Niu, Y., et al. (2020) · Journal of the American Society of Nephrology · doi:10.1681/asn.2020030286 · Cited by 47
Hypoxia and hypoxia-inducible factors in myeloid cell-driven host defense and tissue homeostasis
Jantsch, J., & Schödel, J. (2015) · Immunobiology · doi:10.1016/j.imbio.2014.09.009 · Cited by 46
A potent PGK1 antagonist reveals PGK1 regulates the production of IL-1β and IL-6
Liao, L., Dang, W., Lin, T., Yu, J., Liu, T., Li, W., Xiao, S.-H., Feng, L., Huang, J., Fu, R., et al. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.05.012 · Cited by 45
Wu, M., Zhang, M., Ma, Y., Liu, F., Chen, S., Lu, J., & Chen, H. (2019) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2019.06.010 · Cited by 46
The Role of Metabolic Enzymes in the Regulation of Inflammation
Godfrey, W. H., & Kornberg, M. D. (2020) · Metabolites · doi:10.3390/metabo10110426 · Cited by 50
Mitochondrial complex II in intestinal epithelial cells regulates T cell-mediated immunopathology
Fujiwara, H., Seike, K., Brooks, M. D., Mathew, A. V., Kovalenko, I., Pal, A., Lee, H., Peltier, D., Kim, S. H., Liu, C., et al. (2021) · Nature Immunology · doi:10.1038/s41590-021-01048-3 · Cited by 45
Glycolytic reprogramming by TLRs in dendritic cells
O'Neill, L. A. J. (2014) · Nature Immunology · doi:10.1038/ni.2852 · Cited by 45
Initiation of innate immune responses by surveillance of homeostasis perturbations
Colaço, H. G., & Moita, L. F. (2016) · FEBS Journal · doi:10.1111/febs.13730 · Cited by 45
Mallama, C. A., McCoy-Simandle, K., & Cianciotto, N. P. (2017) · Infection and Immunity · doi:10.1128/iai.00897-16 · Cited by 43
The Cytokine Response to Lipopolysaccharide Does Not Predict the Host Response to Infection
Fensterheim, B. A., Guo, Y., Sherwood, E. R., & Bohannon, J. K. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1602106 · Cited by 47
NOD1 and NOD2: Molecular targets in prevention and treatment of infectious diseases
Pashenkov, M. V., Dagil, Y. A., & Pinegin, B. V. (2017) · International Immunopharmacology · doi:10.1016/j.intimp.2017.11.036 · Cited by 48
Adapted Immune Responses of Myeloid-Derived Cells in Fatty Liver Disease
Hundertmark, J., Krenkel, O., & Tacke, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02418 · Cited by 46
Cao, K., Zhang, T., Li, Z., Song, M., Li, A., Yan, J., Guo, S., Wang, L., Huang, S., Li, Z., et al. (2023) · The Journal of Pathology · doi:10.1002/path.6052 · Cited by 45
Self-citation
Metadata
- Authors
- Everts, B., Amiel, E., Huang, S. C.-C., Smith, A. M., Chang, C.-H., Lam, W. Y., Redmann, V., Freitas, T. C., Blagih, J., van der Windt, G. J. W., Artyomov, M. N., Jones, R. G., Pearce, E. L., & Pearce, E. J.
- Affiliations
- Washington University in St. Louis (US)
- University of Vermont (US)
- Trudeau Institute (US)
- McGill University (CA)
- Corresponding author
- Pearce, Erika L
- Pearce, Edward J
- ORCID
- Venue
- Nature Immunology
- Published
- 2014-02-23
- Volume
- 15
- Issue
- 4
- Pages
- 323-332
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC4358322
- OpenAlex
- W2054828149
- Cited by
- 1,064
- References
- 48
- Citations by year
- 2026: 75 · 2025: 84 · 2024: 89 · 2023: 99 · 2022: 93 · 2021: 119 · 2020: 127 · 2019: 97 · 2018: 81 · 2017: 72 · 2016: 61 · 2015: 44 · 2014: 21
- FWCI
- 30.13
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Funders
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek
- National Institutes of Health
- National Cancer Institute (CA158823, CA164062, R21CA158823, R01CA164062)
- National Institute of Allergy and Infectious Diseases (R01AI091965, AI049823, T32AI049823, R01AI053825, AI53825)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Keywords
- dendritic cell activation, glycolytic reprogramming, Toll-like receptor signaling, TBK1, IKKε, Akt, hexokinase 2, fatty acid synthesis, mitochondrial association, endoplasmic reticulum expansion, Golgi apparatus, dendritic cell metabolism, oxidative phosphorylation
- MeSH terms
- Animals, Cell Differentiation, Cells, Cultured, Dendritic Cells, Fatty Acids, Glycolysis, Hexokinase, Lipopolysaccharides, Lymphocyte Activation, Mice, Inbred C57BL, Mice, Transgenic, T-Lymphocytes, Signal Transduction, Protein Serine-Threonine Kinases, Mice, Knockout, RNA, Small Interfering, Proto-Oncogene Proteins c-akt, Toll-Like Receptors, Mice, I-kappa B Kinase
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