Glycometabolic Reprogramming of Microglia in Neurodegenerative Diseases: Insights from Neuroinflammation
Open accessAbstract
Neurodegenerative diseases (ND) are conditions defined by progressive deterioration of the structure and function of the nervous system. Some major examples include Alzheimer's disease (AD), Parkinson's disease (PD), and Amyotrophic lateral sclerosis (ALS). These diseases lead to various dysfunctions, like impaired cognition, memory, and movement. Chronic neuroinflammation may underlie numerous neurodegenerative disorders. Microglia, an important immunocell in the brain, plays a vital role in defending against neuroinflammation. When exposed to different stimuli, microglia are activated and assume different phenotypes, participating in immune regulation of the nervous system and maintaining tissue homeostasis. The immunological activity of activated microglia is affected by glucose metabolic alterations. However, in the context of chronic neuroinflammation, specific alterations of microglial glucose metabolism and their mechanisms of action remain unclear. Thus, in this paper, we review the glycometabolic reprogramming of microglia in ND. The key molecular targets and main metabolic pathways are the focus of this research. Additionally, this study explores the mechanisms underlying microglial glucose metabolism reprogramming in ND and offers an analysis of the most recent therapeutic advancements. The ultimate aim is to provide insights into the development of potential treatments for ND.
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
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?
Metabolites such as lipid, free fatty acid, and glucose are capable of stimulating microglia and metabolic reprogramming has inherent linkage with microglial activation.
“Recently, acuumulating evidence show that metabolites such as lipid, free fatty acid, and glucose are capable of stimulating microglia and metabolic reprogramming has inherent linkage with microglial activation (immunobolism) [17–20].”
From HIV-TAT dysregulates microglial lipid metabolism through SREBP2/miR-124 axis: Implication of lipid droplet accumulation microglia in NeuroHIV (2025) · cites this paper as [20]
The Abstract (page unavailable) links microglial metabolic reprogramming to immune metabolism and names glucose and fatty acid metabolism. The section “Microglia activation influences glucose metabolism” (page unavailable) describes a close association between metabolism and activation. But the cited passages do not establish that lipids, free fatty acids, or glucose themselves stimulate microglia; they describe increased glucose uptake after activation and activation by inflammatory stimuli or misfolded proteins. (LLM, conf=0.86)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
1 retracted
RETRACTED: mTORC1-Induced HK1-Dependent Glycolysis Regulates NLRP3 Inflammasome Activation
Moon, J.-S., Hisata, S., Park, M. A., DeNicola, G. M., Ryter, S. W., Nakahira, K., & Choi, A. M. K. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.05.046 · Cited by 370 · see citing works
RetractedUnderstanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197 · see citing works
Rosen, D. R., Siddique, T., Patterson, D., Figlewicz, D. A., Sapp, P., Hentati, A., Donaldson, D., Goto, J., O'Regan, J. P., Deng, H.-X., et al. (1993) · Nature · doi:10.1038/362059a0 · Cited by 7,062 · see citing works
Targeting HIF-1 for cancer therapy
Semenza, G. L. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1187 · Cited by 6,717 · cited 2× · see citing works
“HIF-1α, a critical component of the hypoxia response, regulates key glycolytic enzymes, such as GLUT-1, HK2 and LDH, contributing to the metabolic shift from OXPHOS to glycolysis in microglia [82, 84].”
BackgroundResting microglial cells are highly dynamic surveillants of brain parenchyma in vivo
Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827 · see citing works
A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
Keren-Shaul, H., Spinrad, A., Weiner, A., Matcovitch-Natan, O., Dvir-Szternfeld, R., Ulland, T. K., David, E., Baruch, K., Lara-Astaiso, D., Toth, B., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.018 · Cited by 5,493 · see citing works
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175 · see citing works
Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875 · cited 1× · see citing works
“In microglia, LDHB is significantly expressed [71, 72], particularly in the adult hippocampus, where it is mostly exclusive to this cell type compared to others [73].”
BackgroundAMPK: guardian of metabolism and mitochondrial homeostasis
Herzig, S., & Shaw, R. J. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.95 · Cited by 4,094 · see citing works
TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival
Inoki, K., Zhu, T., & Guan, K.-L. (2003) · Cell · doi:10.1016/s0092-8674(03)00929-2 · Cited by 3,914 · see citing works
Kim, J.-W., Tchernyshyov, I., Semenza, G. L., & Dang, C. V. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.02.002 · Cited by 3,905 · see citing works
AMPK Phosphorylation of Raptor Mediates a Metabolic Checkpoint
Gwinn, D. M., Shackelford, D. B., Egan, D. F., Mihaylova, M. M., Mery, A., Vasquez, D. S., Turk, B. E., & Shaw, R. J. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.03.003 · Cited by 3,849 · see citing works
Interplay between Cortical Spreading Depolarization and Seizures
Kramer, D. R., Fujii, T., Ohiorhenuan, I. E., & Liu, C. Y. (2017) · Stereotactic and Functional Neurosurgery · doi:10.1159/000452841 · Cited by 3,718 · see citing works
Mechanisms underlying inflammation in neurodegeneration
Glass, C. K., Saijo, K., Winner, B., Marchetto, M. C., & Gage, F. H. (2010) · Cell · doi:10.1016/j.cell.2010.02.016 · Cited by 3,580 · see citing works
An Energy Budget for Signaling in the Grey Matter of the Brain
Attwell, D., & Laughlin, S. B. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200110000-00001 · Cited by 3,543 · see citing works
Neuroinflammation and microglial activation in Alzheimer disease: where do we go from here?
Leng, F., & Edison, P. (2021) · Nature Reviews Neurology · doi:10.1038/s41582-020-00435-y · Cited by 3,179 · see citing works
Microglia Function in the Central Nervous System During Health and Neurodegeneration
Colonna, M., & Butovsky, O. (2017) · Annual Review of Immunology · doi:10.1146/annurev-immunol-051116-052358 · Cited by 2,894 · see citing works
Neuroinflammation in neurodegenerative disorders: the roles of microglia and astrocytes
Kwon, H. S., & Koh, S.-H. (2020) · Translational Neurodegeneration · doi:10.1186/s40035-020-00221-2 · Cited by 2,595 · see citing works
Oxidative Stress: A Key Modulator in Neurodegenerative Diseases
Singh, A., Kukreti, R., Saso, L., & Kukreti, S. (2019) · Molecules · doi:10.3390/molecules24081583 · Cited by 2,305 · see citing works
Hardiman, O. M., Al‐Chalabi, A., Chiò, A., Corr, E. M., Logroscino, G., Robberecht, W., Shaw, P. J., Simmons, Z., & van den Berg, L. H. (2017) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2017.71 · Cited by 2,191 · see citing works
Decreased Clearance of CNS β-Amyloid in Alzheimer’s Disease
Mawuenyega, K. G., Sigurdson, W., Ovod, V., Munsell, L., Kasten, T., Morris, J. C., Yarasheski, K. E., & Bateman, R. J. (2010) · Science · doi:10.1126/science.1197623 · Cited by 2,078 · see citing works
Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain
Lawson, L. J., Perry, V. H., Dri, P., & Gordon, S. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90229-w · Cited by 2,045 · see citing works
Microglia and macrophages in brain homeostasis and disease
Li, Q., & Barres, B. A. (2018) · Nature Reviews Immunology · doi:10.1038/nri.2017.125 · Cited by 1,999 · see citing works
TREM2 Lipid Sensing Sustains the Microglial Response in an Alzheimer’s Disease Model
Wang, Y., Cella, M., Mallinson, K., Ulrich, J. D., Young, K. L., Robinette, M. L., Gilfillan, S., Krishnan, G. M., Sudhakar, S., Zinselmeyer, B. H., et al. (2015) · Cell · doi:10.1016/j.cell.2015.01.049 · Cited by 1,736 · see citing works
Self-citationSugar for the brain: the role of glucose in physiological and pathological brain function
Mergenthaler, P., Lindauer, U., Dienel, G. A., & Meisel, A. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.07.001 · Cited by 1,612 · see citing works
Disease-Associated Microglia: A Universal Immune Sensor of Neurodegeneration
Deczkowska, A., Keren-Shaul, H., Weiner, A., Colonna, M., Schwartz, M., & Amit, I. (2018) · Cell · doi:10.1016/j.cell.2018.05.003 · Cited by 1,474 · see citing works
Hu, X.-M., Li, P.-Y., Guo, Y., Wang, H., Leak, R., Chen, S., Gao, Y.-Q., & Chen, J. (2012) · Stroke · doi:10.1161/strokeaha.112.659656 · Cited by 1,445 · see citing works
Self-citationRepertoire of microglial and macrophage responses after spinal cord injury
David, S., & Kroner, A. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3053 · Cited by 1,437 · see citing works
Zhang, W., Wang, T., Pei, Z., Miller, D. S., Wu, X., Block, M. L., Wilson, B., Zhang, W., Zhou, Y., Hong, J.-S., et al. (2005) · The FASEB Journal · doi:10.1096/fj.04-2751com · Cited by 1,265 · see citing works
TREM2 Maintains Microglial Metabolic Fitness in Alzheimer’s Disease
Ulland, T. K., Song, W. M., Huang, S. C.-C., Ulrich, J. D., Sergushichev, A., Beatty, W. L., Loboda, A. A., Zhou, Y., Cairns, N. J., Kambal, A., et al. (2017) · Cell · doi:10.1016/j.cell.2017.07.023 · Cited by 1,263 · see citing works
Self-citationIn vivo imaging of microglial activation with [11C](R)-PK11195 PET in idiopathic Parkinson's disease
Gerhard, A., Pavese, N., Hotton, G., Turkheimer, F., Es, M., Hammers, A., Eggert, K., Oertel, W., Banati, R. B., & Brooks, D. J. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2005.08.002 · Cited by 1,200 · see citing works
Making new contacts: the mTOR network in metabolism and signalling crosstalk
Shimobayashi, M., & Hall, M. N. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3757 · Cited by 1,053 · see citing works
Johnson, E. C. B., Dammer, E. B., Duong, D. M., Ping, L., Zhou, M., Yin, L., Higginbotham, L. A., Guajardo, A., White, B., Troncoso, J. C., et al. (2020) · Nature Medicine · doi:10.1038/s41591-020-0815-6 · Cited by 1,001 · see citing works
Inflammation in CNS neurodegenerative diseases
Stephenson, J., Nutma, E., van der Valk, P., & Amor, S. (2018) · Immunology · doi:10.1111/imm.12922 · Cited by 966 · see citing works
Yeh, F. L., Wang, Y., Tom, I., Gonzalez, L. C., & Sheng, M. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.015 · Cited by 943 · see citing works
Self-citationButovsky, O., Ziv, Y., Schwartz, A., Landa, G., Talpalar, A. E., Pluchino, S., Martino, G., & Schwartz, M. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.10.006 · Cited by 923 · see citing works
Microglia polarization from M1 to M2 in neurodegenerative diseases
Guo, S., Wang, H., & Yin, Y. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.815347 · Cited by 920 · see citing works
Microglia-mediated neuroinflammation in neurodegenerative diseases
Subhramanyam, C. S., Wang, C., Hu, Q., & Dheen, S. T. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.05.004 · Cited by 875 · see citing works
Pan, R.-Y., He, L., Zhang, J., Liu, X., Liao, Y., Gao, J., Liao, Y., Yan, Y., Li, Q., Zhou, X., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.02.013 · Cited by 862 · see citing works
A Breakdown in Metabolic Reprogramming Causes Microglia Dysfunction in Alzheimer's Disease
Baik, S. H., Kang, S., Lee, W., Choi, H., Chung, S., Kim, J.-I., & Mook-Jung, I. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.06.005 · Cited by 843 · see citing works
Regulation and metabolic functions of mTORC1 and mTORC2
Szwed, A., Kim, E., & Jacinto, E. (2021) · Physiological Reviews · doi:10.1152/physrev.00026.2020 · Cited by 826 · see citing works
Sağ, D., Carling, D., Stout, R. D., & Suttles, J. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.12.8633 · Cited by 798 · see citing works
Monocarboxylate transporters in the central nervous system: distribution, regulation and function
Pierre, K., & Pellerin, L. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03168.x · Cited by 744 · see citing works
Regional aerobic glycolysis in the human brain
Vaishnavi, S. N., Vlassenko, A. G., Rundle, M. M., Snyder, A. Z., Mintun, M. A., & Raichle, M. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010459107 · Cited by 738 · see citing works
Turner, M. R., Cagnin, A., Turkheimer, F. E., Miller, C. C. J., Shaw, C. E., Brooks, D. J., Leigh, P. N., & Banati, R. B. (2004) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.12.012 · Cited by 737 · see citing works
Phagocytosis of Microglia in the Central Nervous System Diseases
Fu, R., Shen, Q., Xu, P., Luo, J. J., & Tang, Y. (2014) · Molecular Neurobiology · doi:10.1007/s12035-013-8620-6 · Cited by 646 · see citing works
Nitric oxide synthase and neuronal vulnerability in parkinson's disease
Hunot, S., Boissière, F., Faucheux, B., Brugg, B., Mouatt-Prigent, A., Agid, Y., & Hirsch, E. C. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00578-1 · Cited by 595 · see citing works
Restoring metabolism of myeloid cells reverses cognitive decline in ageing
Minhas, P. S., Latif-Hernandez, A., McReynolds, M. R., Durairaj, A. S., Wang, Q., Rubin, A., Joshi, A. U., He, J. Q., Gauba, E., Liu, L., et al. (2021) · Nature · doi:10.1038/s41586-020-03160-0 · Cited by 526 · see citing works
Fighting neurodegeneration with rapamycin: mechanistic insights
Bové, J., Martínez‐Vicente, M., & Vila, M. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3068 · Cited by 525 · see citing works
Inflammatory processes in amyotrophic lateral sclerosis
McGeer, P. L., & McGeer, E. G. (2002) · Muscle & Nerve · doi:10.1002/mus.10191 · Cited by 470 · see citing works
Cosenza‐Nashat, M., Zhao, M. ‐., Suh, H. ‐., Morgan, J., Natividad, R., Morgello, S., & Lee, S. C. (2009) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2008.01006.x · Cited by 459 · cited 1× · see citing works
“The high expression of the translocator protein (TSPO) in the outer membrane of mitochondria is widely recognized as a characteristic feature of neuroinflammation, particularly in activated microglia [158].”
BackgroundTREM2, microglia, and neurodegenerative diseases
Yeh, F. L., Hansen, D. V., & Sheng, M. (2017) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2017.03.008 · Cited by 440 · cited 2× · see citing works
“Currently, there are no in vivo examples of drugs specifically targeting TREM2 agonism for treating ND like AD and PD, and this approach may still present challenges [151].”
BackgroundLactate is always the end product of glycolysis
Rogatzki, M. J., Ferguson, B. S., Goodwin, M. L., & Gladden, L. B. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00022 · Cited by 428 · see citing works
Lactylation of PKM2 Suppresses Inflammatory Metabolic Adaptation in Pro-inflammatory Macrophages
Wang, J., Yang, P., Yu, T., Gao, M., Liu, D., Zhang, J., Lu, C., Chen, X., Zhang, X., & Liu, Y. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.75434 · Cited by 413 · see citing works
Spatial correlation between brain aerobic glycolysis and amyloid-β (Aβ) deposition
Vlassenko, A. G., Vaishnavi, S. N., Couture, L., Sacco, D., Shannon, B. J., Mach, R. H., Morris, J. C., Raichle, M. E., & Mintun, M. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010461107 · Cited by 404 · see citing works
Lee, C. Y. D., Daggett, A., Gu, X., Jiang, L.-L., Langfelder, P., Li, X., Wang, N., Zhao, Y., Park, C. S., Cooper, Y., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.02.002 · Cited by 396 · see citing works
Inflammatory neuroprotection following traumatic brain injury
Russo, M. V., & McGavern, D. B. (2016) · Science · doi:10.1126/science.aaf6260 · Cited by 380 · see citing works
Glucose transporter 1 critically controls microglial activation through facilitating glycolysis
Wang, L., Pavlou, S., Du, X., Bhuckory, M. B., Xu, H., & Chen, M. (2019) · Molecular Neurodegeneration · doi:10.1186/s13024-019-0305-9 · Cited by 334 · see citing works
Pinto, A. R., Paolicelli, R., Salimova, E., Gospocic, J., Slonimsky, E., Bilbao-Cortes, D., Godwin, J. W., & Rosenthal, N. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036814 · Cited by 318 · see citing works
Metabolic Reprograming of Microglia in the Regulation of the Innate Inflammatory Response
Lauro, C., & Limatola, C. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00493 · Cited by 315 · see citing works
Devanney, N. A., Stewart, A. N., & Gensel, J. C. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113310 · Cited by 311 · see citing works
Cassina, P., Cassina, A., Pehar, M., Castellanos, R., Gandelman, M., de León, A., Robinson, K. M., Mason, R. P., Beckman, J. S., Barbeito, L., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5308-07.2008 · Cited by 310 · see citing works
Battista, D., Ferrari, C. C., Gage, F. H., & Pitossi, F. J. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04539.x · Cited by 306 · see citing works
Early glycolytic reprogramming controls microglial inflammatory activation
Cheng, J., Zhang, R., Xu, Z., Ke, Y., Sun, R., Yang, H., Zhang, X., Zhen, X., & Zheng, L.-T. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02187-y · Cited by 295 · see citing works
Bioenergetic regulation of microglia
Ghosh, S., Castillo, E., Frias, E. S., & Swanson, R. A. (2017) · Glia · doi:10.1002/glia.23271 · Cited by 290 · see citing works
Pan, R., Ma, J., Kong, X.-X., Wang, X., Li, S., Qi, X., Yan, Y., Cheng, J., Liu, Q., Jin, W., et al. (2019) · Science Advances · doi:10.1126/sciadv.aau6328 · Cited by 290 · see citing works
Unappreciated Role of LDHA and LDHB to Control Apoptosis and Autophagy in Tumor Cells
Urbańska, K., & Orzechowski, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092085 · Cited by 288 · see citing works
Microglial Polarization and Inflammatory Mediators After Intracerebral Hemorrhage
Zhang, Z., Zhang, Z., Lu, H., Yang, Q., Wu, H., & Wang, J. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9785-6 · Cited by 276 · see citing works
Nair, S., Sobotka, K. S., Joshi, P., Gressèns, P., Fleiss, B., Thornton, C., Mallard, C. E., & Hagberg, H. (2019) · Glia · doi:10.1002/glia.23587 · Cited by 274 · see citing works
Chen, R., Lai, U. H., Zhu, L., Singh, A., AlKataan, M. A. A., & Forsyth, N. R. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00132 · Cited by 272 · see citing works
Pellerin, L., Halestrap, A. P., & Pierre, K. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20307 · Cited by 269 · see citing works
Xiang, X., Wind, K., Wiedemann, T., Blume, T., Shi, Y., Briel, N., Beyer, L., Biechele, G., Eckenweber, F., Zatcepin, A., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abe5640 · Cited by 268 · see citing works
Michinaga, S., & Koyama, Y. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030571 · Cited by 263 · see citing works
Hu, Y., Mai, W., Chen, L., Cao, K., Zhang, B., Zhang, Z., Liu, Y., Lou, H., Duan, S., & Gao, Z. (2019) · Glia · doi:10.1002/glia.23760 · Cited by 256 · see citing works
The changing phenotype of microglia from homeostasis to disease
Luo, X., & Chen, S. (2012) · Translational Neurodegeneration · doi:10.1186/2047-9158-1-9 · Cited by 233 · see citing works
Self-citationvan Lengerich, B., Zhan, L., Xia, D., Chan, D., Joy, D., Park, J. I., Tatarakis, D., Calvert, M., Hummel, S., Lianoglou, S., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-022-01240-0 · Cited by 233 · see citing works
Microglia reprogram metabolic profiles for phenotype and function changes in central nervous system
Yang, S., Qin, C., Hu, Z.-W., Zhou, L.-Q., Yu, H.-H., Chen, M., Bosco, D. B., Wang, W., Wu, L.-J., & Tian, D.-S. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105290 · Cited by 232 · see citing works
Voloboueva, L. A., Emery, J. F., Sun, X., & Giffard, R. G. (2013) · FEBS Letters · doi:10.1016/j.febslet.2013.01.067 · Cited by 230 · see citing works
TREM2, microglia, and Alzheimer’s disease.
Qin, Q., Teng, Z., Liu, C., Li, Q., Yin, Y., & Tang, Y. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111438 · Cited by 219 · see citing works
Inflammatory microglia are glycolytic and iron retentive and typify the microglia in APP/PS1 mice
Holland, R., McIntosh, A. L., Finucane, O. M., Mela, V., Rubio‐Araiz, A., Timmons, G. A., McCarthy, S. A., Gun’ko, Y. K., & Lynch, M. A. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.10.017 · Cited by 217 · see citing works
Glucose pathways adaptation supports acquisition of activated microglia phenotype
Gimeno‐Bayón, J., López‐López, A., Rodríguez, M. J., & Mahy, N. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23356 · Cited by 213 · see citing works
Neuroinflammation — a common thread in neurological disorders
Gilhus, N. E., & Deuschl, G. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0227-8 · Cited by 198 · see citing works
Leng, L., Yuan, Z., Pan, R., Su, X., Wang, H., Xue, J., Zhuang, K., Gao, J., Chen, Z., Lin, H. Z., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00643-4 · Cited by 193 · see citing works
McIntosh, A. L., Mela, V., Harty, C., Minogue, A. M., Costello, D. A., Kerskens, C., & Lynch, M. A. (2019) · Brain Pathology · doi:10.1111/bpa.12704 · Cited by 190 · see citing works
Zhu, Y. P., Brown, J. R., Sağ, D., Zhang, L., & Suttles, J. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1401024 · Cited by 186 · see citing works
Association of Regulatory T-Cell Expansion With Progression of Amyotrophic Lateral Sclerosis
Sheean, R. K., McKay, F. C., Cretney, E., Bye, C. R., Perera, N. D., Tomas, D., Weston, R. A., Scheller, K. J., Djouma, E., Menon, P., et al. (2018) · JAMA Neurology · doi:10.1001/jamaneurol.2018.0035 · Cited by 177 · see citing works
Microglia and C9orf72 in neuroinflammation and ALS and frontotemporal dementia
Lall, D., & Baloh, R. H. (2017) · Journal of Clinical Investigation · doi:10.1172/jci90607 · Cited by 175 · cited 1× · see citing works
“Research on adult family lineages has identified specific gene mutations, including SOD1, C9orf72, TDP43, and FUS74, which are associated with the heritability of ALS [112, 113].”
BackgroundHu, Y., Cao, K., Wang, F., Wu, W., Mai, W., Qiu, L., Luo, Y., Ge, W., Sun, B., Shi, L., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00707-5 · Cited by 175 · see citing works
Oncoprotein Akt/PKB induces trophic effects in murine models of Parkinson's disease
Ries, V., Henchcliffe, C., Kareva, T., Rzhetskaya, M., Bland, R. J., During, M. J., Kholodilov, N. G., & Burke, R. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606401103 · Cited by 168 · see citing works
Role of Mitochondrial Membrane Potential and Lactate Dehydrogenase A in Apoptosis
Zaib, S., Khan, I. A., Hayyat, A., Ali, N., Gul, A., & Naveed, M. (2021) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520621666211126090906 · Cited by 167 · see citing works
Hsieh, C., Liu, C., Lee, C., Yu, L.-E., & Wang, J. (2019) · Scientific Reports · doi:10.1038/s41598-018-37215-0 · Cited by 156 · see citing works
Microglia promote glioblastoma via mTOR‐mediated immunosuppression of the tumour microenvironment
Dumas, A. A., Pomella, N., Rosser, G., Guglielmi, L., Vinel, C., Millner, T. O., Rees, J. H., Aley, N., Sheer, D., Wei, J., et al. (2020) · The EMBO Journal · doi:10.15252/embj.2019103790 · Cited by 155 · see citing works
Ligand for Translocator Protein Reverses Pathology in a Mouse Model of Alzheimer's Disease
Barron, A. M., García‐Segura, L. M., Caruso, D., Jayaraman, A., Lee, J.-W., Melcangi, R. C., & Pike, C. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1350-13.2013 · Cited by 153 · see citing works
Microglia-Specific Metabolic Changes in Neurodegeneration
Aldana, B. I. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.03.006 · Cited by 153 · see citing works
Brain energy metabolism: Astrocytes in neurodegenerative diseases.
Chen, Z., Yuan, Z., Yang, S., Zhu, Y., Xue, M., Zhang, J., & Leng, L. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13982 · Cited by 153 · see citing works
The pentose phosphate pathway regulates chronic neuroinflammation and dopaminergic neurodegeneration
Tu, D., Gao, Y., Yang, R., Guan, T., Hong, J., & Gao, H. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1659-1 · Cited by 150 · see citing works
Liu, B., Zhang, Y., Yang, Z., Liu, M., Zhang, C., Zhao, Y., & Song, C. (2021) · Marine Drugs · doi:10.3390/md19110587 · Cited by 146 · see citing works
Poulain, L., Sujobert, P., Zylbersztejn, F., Barreau, S., Stuani, L., Lambert, M., Palama, T. L., Chesnais, V, Birsen, R., Vergez, F., et al. (2017) · Leukemia · doi:10.1038/leu.2017.81 · Cited by 145 · see citing works
Enzymatic dissociation induces transcriptional and proteotype bias in brain cell populations
Mattei, D., Ivanov, A., van Oostrum, M., Pantelyushin, S., Richetto, J., Mueller, F., Beffinger, M. M., Schellhammer, L., vom Berg, J., Wollscheid, B., et al. (2020) · doi:10.1101/2020.05.14.095422 · Cited by 143 · see citing works
Zhang, S., Zhu, L., Peng, Y., Zhang, L., Chao, F., Jiang, L. H., Xiao, Q., Liang, X., Tang, J., Yang, H., et al. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02401-5 · Cited by 143 · see citing works
Piers, T. M., Cosker, K., Mallach, A., Johnson, G. T., Guerreiro, R., Hardy, J., & Pocock, J. M. (2020) · The FASEB Journal · doi:10.1096/fj.201902447r · Cited by 135 · see citing works
TRPV1 on astrocytes rescues nigral dopamine neurons in Parkinson’s disease via CNTF
Nam, J. H., Park, E. S., Won, S.-Y., Lee, Y. A., Kim, K. I., Jeong, J. Y., Baek, J. Y., Cho, E. J., Jin, M., Chung, Y. C., et al. (2015) · Brain · doi:10.1093/brain/awv297 · Cited by 134 · see citing works
The role of microglial activation in disease progression
Correale, J. D. (2014) · Multiple Sclerosis Journal · doi:10.1177/1352458514533230 · Cited by 133 · see citing works
Nitrated Alpha-Synuclein and Microglial Neuroregulatory Activities
Reynolds, A. D., Kadiu, I., Garg, S. K., Glanzer, J. G., Nordgren, T. M., Ciborowski, P. S., Banerjee, R. V., & Gendelman, H. E. (2008) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-008-9100-z · Cited by 128 · see citing works
Fairley, L. H., Lai, K. O., Wong, J. H., Chong, W. J., Vincent, A. S., D’Agostino, G. A., Wu, X., Naik, R. R., Jayaraman, A., Langley, S. R., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2209177120 · Cited by 127 · see citing works
Zhang, F., Zhong, R., Li, S., Fu, Z., Cheng, C., Cai, H., & Le, W. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00282 · Cited by 125 · see citing works
Hypoxia compromises the mitochondrial metabolism of Alzheimer’s disease microglia via HIF1
March-Diaz, R., Lara-Ureña, N., Romero-Molina, C., Heras-Garvin, A., Ortega-de San Luis, C., Alvarez-Vergara, M. I., Sanchez-Garcia, M. A., Sanchez-Mejias, E., Davila, J. C., Rosales-Nieves, A. E., et al. (2021) · Nature Aging · doi:10.1038/s43587-021-00054-2 · Cited by 125 · see citing works
Enzymatic Dissociation Induces Transcriptional and Proteotype Bias in Brain Cell Populations
Mattei, D., Ivanov, A., van Oostrum, M., Pantelyushin, S., Richetto, J., Mueller, F., Beffinger, M., Schellhammer, L., vom Berg, J., Wollscheid, B., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217944 · Cited by 123 · see citing works
Differential contribution of microglia and monocytes in neurodegenerative diseases
Baufeld, C., O'Loughlin, E. K., Calcagno, N., Madore, C., & Butovsky, O. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1795-7 · Cited by 123 · see citing works
TRPV1 sustains microglial metabolic reprogramming in Alzheimer's disease
Lu, J., Zhou, W., Dou, F., Wang, C., & Yu, Z. (2021) · The EMBO Reports · doi:10.15252/embr.202052013 · Cited by 121 · see citing works
Chung, Y. C., Baek, J. Y., Kim, S. R., Ko, H. W., Bok, E., Shin, W.-H., Won, S.-Y., & Jin, B. K. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2016.159 · Cited by 121 · see citing works
Mitochondrial Regulation of Microglial Immunometabolism in Alzheimer’s Disease
Fairley, L. H., Wong, J. H., & Barron, A. M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.624538 · Cited by 120 · see citing works
CNS glucose metabolism in Amyotrophic Lateral Sclerosis: a therapeutic target?
Tefera, T. W., Steyn, F. J., Ngo, S. T., & Borges, K. (2021) · Cell & Bioscience · doi:10.1186/s13578-020-00511-2 · Cited by 118 · see citing works
Liu, Y., Hao, W., Dawson, A., Liu, S., & Fassbender, K. C. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804446200 · Cited by 117 · see citing works
Rubio‐Araiz, A., Finucane, O. M., Keogh, S., & Lynch, M. A. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1281-7 · Cited by 114 · see citing works
Toll‐like receptors in neuroinflammation, neurodegeneration, and alcohol‐induced brain damage
Pascual, M., Calvo-Rodríguez, M., Núñez, L., Villalobos, C., Ureña, J., & Guerri, C. (2021) · IUBMB Life · doi:10.1002/iub.2510 · Cited by 114 · see citing works
Kong, L., Wang, Z., Liang, X., Wang, Y., Gao, L., & Ma, C. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1648-4 · Cited by 113 · see citing works
Self-citationMicroglial metabolic flexibility: emerging roles for lactate
Monsorno, K., Buckinx, A., & Paolicelli, R. C. (2022) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2021.12.001 · Cited by 113 · see citing works
Moreira, T. J., Pierre, K., Maekawa, F., Repond, C., Cebere, A., Liljequist, S., & Pellerin, L. (2009) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.50 · Cited by 112 · see citing works
Sapin, E., Peyron, C., Roche, F., Gay, N., Carcenac, C., Savasta, M., Levy, P. A., & Demattéis, M. (2015) · SLEEP · doi:10.5665/sleep.5042 · Cited by 112 · see citing works
Increased Glucose Transport into Neurons Rescues Aβ Toxicity in Drosophila
Niccoli, T., Cabecinha, M., Tillmann, A., Kerr, F., Wong, C. T., Cardenes, D., Vincent, A. J., Bettedi, L., Li, L., Grönke, S., et al. (2016) · Current Biology · doi:10.1016/j.cub.2016.07.017 · Cited by 111 · see citing works
Hou, L., Sun, F., Huang, R., Sun, W., Zhang, D., & Wang, Q. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101134 · Cited by 110 · see citing works
Mela, V., Mota, B. C., Milner, M. T., McGinley, A. M., Mills, K. H. G., Kelly, Á. M., & Lynch, M. A. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.01.012 · Cited by 98 · see citing works
Gu, C., Wang, F., Zhang, Y., Wei, S., Liu, J., Sun, H., Wang, G., & Liu, C. (2021) · Aging Cell · doi:10.1111/acel.13375 · Cited by 98 · see citing works
Weise, C. M., Chen, K., Chen, Y., Kuang, X., Savage, C. R., & Reiman, E. M. (2018) · NeuroImage: Clinical · doi:10.1016/j.nicl.2018.07.016 · Cited by 96 · see citing works
Du, Y., Fu, M., Huang, Z., Tian, X., Li, J., Pang, Y., Song, W., Tian Wang, Y., & Dong, Z. (2020) · Aging Cell · doi:10.1111/acel.13113 · Cited by 95 · see citing works
Self-citationSchilling, S., Chausse, B., Dikmen, H. O., Almouhanna, F., Hollnagel, J., Lewen, A., & Kann, O. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.05.013 · Cited by 91 · see citing works
Hexokinases in cancer and other pathologies
Guo, D. S., Meng, Y., Jiang, X., & Lu, Z. (2023) · Cell Insight · doi:10.1016/j.cellin.2023.100077 · Cited by 91 · see citing works
Habib, P., Slowik, A., Zendedel, A., Johann, S., Dang, J., & Beyer, C. (2014) · Journal of Molecular Neuroscience · doi:10.1007/s12031-013-0137-y · Cited by 88 · see citing works
Early effects of LPS-induced neuroinflammation on the rat hippocampal glycolytic pathway
Vizuete, A. F. K., Fróes, F. T., Seady, M., Zanotto, C., Bobermin, L. D., Roginski, A. C., Wajner, M., Quincozes‐Santos, A., & Gonçalves, C. A. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02612-w · Cited by 83 · see citing works
Mechanism and Regulation of Microglia Polarization in Intracerebral Hemorrhage
Guo, Y., Dai, W., Zheng, Y., Qiao, W., Chen, W., Peng, L., Zhou, H., Zhao, T., Liu, H., Zheng, F., et al. (2022) · Molecules · doi:10.3390/molecules27207080 · Cited by 81 · see citing works
Lu, J., Wang, C., Cheng, X., Wang, R., Yan, X., He, P., Chen, H., & Yu, Z. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02484-0 · Cited by 80 · see citing works
Yan, Q., Han, C., Wang, G., Waddington, J. L., Zheng, L., & Zhen, X. (2017) · Molecular Pharmacology · doi:10.1124/mol.117.109512 · Cited by 77 · cited 1× · see citing works
“Metformin exerts its effects by acting upstream of mTOR and targeting AMPK, while rapamycin directly inhibits mTOR expression by binding to mTORC1 [135-137].”
BackgroundHe, Z., Yang, Y., Xing, Z., Zuo, Z., Wang, R., Gu, H., Qi, F., & Yao, Z. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2644-4 · Cited by 77 · see citing works
Imaging Neuroinflammation in Neurodegenerative Disorders
Masdeu, J. C., Pascual, B., & Fujita, M. (2022) · Journal of Nuclear Medicine · doi:10.2967/jnumed.121.263200 · Cited by 76 · see citing works
Chausse, B., Lewen, A., Poschet, G., & Kann, O. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.05.052 · Cited by 74 · see citing works
Role of neuroinflammation and latent transcription factors in pathogenesis of Parkinson’s disease
Pal, R., Tiwari, P. C., Nath, R., & Pant, K. K. (2016) · Neurological Research · doi:10.1080/01616412.2016.1249997 · Cited by 72 · see citing works
Nerve Growth Factor modulates LPS - induced microglial glycolysis and inflammatory responses
Fodelianaki, G., Lansing, F., Bhattarai, P., Troullinaki, M., C., M. A. Z., Charalampopoulos, I., Gravanis, A., Mirtschink, P., Chavakis, T., & Alexaki, V. I. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.02.023 · Cited by 70 · see citing works
Stepanov, Y. V., Golovynska, I., Zhang, R., Golovynskyi, S., Stepanova, L. I., Gorbach, O. I., Dovbynchuk, T., Garmanchuk, L., Ohulchanskyy, T. Y., & Qu, J. (2022) · Alzheimer s Research & Therapy · doi:10.1186/s13195-022-01022-7 · Cited by 68 · see citing works
Divergent Effects of Metformin on an Inflammatory Model of Parkinson’s Disease
Tayara, K., Espinosa‐Oliva, A. M., García-Domínguez, I., Ismaiel, A. A., Boza‐Serrano, A., Deierborg, T., Machado, A., Herrera, A. J., Venero, J. L., & de Pablos, R. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00440 · Cited by 66 · see citing works
Liu, Y., Deng, S., Zhang, Z., Gu, Y., Xia, S., Bao, X., Cao, X., & Xu, Y. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173294 · Cited by 65 · see citing works
Ryu, J. K., Kim, S. U., & McLarnon, J. G. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.01.006 · Cited by 62 · see citing works
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 · see citing works
HK2: Gatekeeping microglial activity by tuning glucose metabolism and mitochondrial functions
Fang, J., Luo, S., & Lu, Z. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.02.022 · Cited by 62 · see citing works
Li, M., Lu, H., Wang, X., Duan, C., Zhu, X., Zhang, Y., Ge, X., Ji, F., Wang, X., Su, J., et al. (2021) · Molecular Immunology · doi:10.1016/j.molimm.2021.10.017 · Cited by 60 · see citing works
Iravanpour, F., Dargahi, L., Rezaei, M., Haghani, M., Heidari, R., Valian, N., & Ahmadiani, A. (2021) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13609 · Cited by 60 · see citing works
Clk1‐regulated aerobic glycolysis is involved in glioma chemoresistance
Zhang, L., Yang, H., Zhang, W., Liang, Z., Huang, Q., Xu, G., Zhen, X., & Zheng, L. T. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14096 · Cited by 55 · see citing works
Self-citationEngeletin Attenuates Aβ1–42-Induced Oxidative Stress and Neuroinflammation by Keap1/Nrf2 Pathway
Huang, Z., Ji, H., Shi, J., Zhu, X., & Zhi, Z. (2020) · Inflammation · doi:10.1007/s10753-020-01250-9 · Cited by 54 · see citing works
Wang, C., Huang, W., Lu, J., Chen, H., & Yu, Z. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.763866 · Cited by 49 · see citing works
Pyrroloquinoline Quinone Inhibits Rotenone-Induced Microglia Inflammation by Enhancing Autophagy
Zhang, Q., Zhou, J., Shen, M., Xu, H., Yu, S., Cheng, Q., & Ding, F. (2020) · Molecules · doi:10.3390/molecules25194359 · Cited by 47 · see citing works
Meng, F., Yu, W., Duan, W., Wang, T., & Liu, Y. (2019) · Fundamental and Clinical Pharmacology · doi:10.1111/fcp.12528 · Cited by 45 · see citing works
Lv, Y., Zhang, B., Zhai, C., Qiu, J. F., Zhang, Y., Yao, W., & Zhang, C. (2015) · Neurochemistry International · doi:10.1016/j.neuint.2015.10.006 · Cited by 44 · see citing works
Microglia immunometabolism: From metabolic disorders to single cell metabolism
Paolicelli, R. C., & Angiari, S. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.03.012 · Cited by 44 · see citing works
Neuronal lactate levels depend on glia‐derived lactate during high brain activity in Drosophila
González‐Gutiérrez, A., Ibacache, A., Esparza, A., Barros, L. F., & Sierralta, J. A. (2019) · Glia · doi:10.1002/glia.23772 · Cited by 43 · see citing works
Hypoxia in Alzheimer’s disease: effects of hypoxia inducible factors
Hassan, H., & Chen, R. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.290898 · Cited by 43 · see citing works
Wei, Y., Chen, J., Cai, G., Lu, W., Xu, W., Wang, R., Lin, Y., & Yang, C. (2020) · Inflammation · doi:10.1007/s10753-020-01314-w · Cited by 41 · see citing works
TSPO ligand PK11195 improves Alzheimer-related outcomes in aged female 3xTg-AD mice
Christensen, A., & Pike, C. J. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.06.029 · Cited by 40 · see citing works
Significance of Microglial Energy Metabolism in Maintaining Brain Homeostasis
Bielanin, J. P., & Sun, D. (2022) · Translational Stroke Research · doi:10.1007/s12975-022-01069-6 · Cited by 37 · see citing works
Li, Q., Peng, J., Luo, Y., Zhou, J., Li, T., Cao, L. S., Peng, S., Zuo, Z., & Wang, Z. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02521-y · Cited by 36 · see citing works
Prognostic Value of Monocarboxylate Transporter 1 Overexpression in Cancer: A Systematic Review
Silva, A., Cerqueira, M. C., Rosa, B., Sobral, C., Pinto‐Ribeiro, F., Costa, M. F., Baltazar, F., & Afonso, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065141 · Cited by 36 · see citing works
Fan, F., Xu, N., Sun, Y., Li, X., Gao, X., Yi, X., Zhang, Y., Meng, X., & Lin, J. (2021) · Journal of Proteome Research · doi:10.1021/acs.jproteome.1c00647 · Cited by 35 · see citing works
Wang, D., Gu, X. Q., Ma, X., Chen, J., Zhang, Q., Yu, Z., Li, J., Meng, H., Tan, X., Tang, Y., et al. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.07.014 · Cited by 35 · see citing works
Honokiol Restores Microglial Phagocytosis by Reversing Metabolic Reprogramming
Li, W., Wang, S., Zhang, H., Li, B., Xu, L., Li, Y., Kong, C., Jiao, H., Wang, Y., Pang, Y., et al. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210177 · Cited by 31 · see citing works
Self-citationDARPP-32 to Quantify Intracerebral Hemorrhage-Induced Neuronal Death in Basal Ganglia
Jin, H., Xi, G., Keep, R. F., Wu, J., & Hua, Y. (2012) · Translational Stroke Research · doi:10.1007/s12975-012-0232-3 · Cited by 31 · see citing works
Ma, X., Zhang, Y., Gou, D., Ma, J., Du, J., Wang, C., Li, S., & Cui, H. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220227 · Cited by 30 · see citing works
Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier
Liu, H., Wei, J., Li, Y., Ban, M., Sun, Q., Wang, H.-J., Zhao, D., Tong, P., Wang, L., Wang, K.-J., et al. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202103098 · Cited by 27 · see citing works
Ji, B., Ono, M., Yamasaki, T., Fujinaga, M., Zhang, M., Seki, C., Aoki, I., Kito, S., Sawada, M., Suhara, T., et al. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x21992457 · Cited by 25 · see citing works
Sun, J., Zhu, K., Wang, Y., Wang, D.-J., Zhang, M.-Z., Sarlus, H., Benito‐Cuesta, I., Zhao, X.-Q., Zou, Z., Zhong, Q.-Y., et al. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-01000-7 · Cited by 24 · see citing works
Self-citationChen, J., Tang, C., Zhou, Y., Zhang, R., Ye, S., Zhao, Z., Lin, L., & Yang, D. (2020) · Molecules · doi:10.3390/molecules25204796 · Cited by 21 · see citing works
Zhang, Y., Li, H., Chen, Y., Fan, D.-F., Guo, D.-Z., Hu, H., Meng, X.-E., & Pan, S. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1750-7 · Cited by 17 · see citing works
Microglia: Same same, but different
Kierdorf, K., & Prinz, M. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20191535 · Cited by 15 · see citing works
Endert, P. V., & Mauvais, F. (2023) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.742491914.793597512 · Cited by 12 · see citing works
Effect of Tau Protein on Mitochondrial Functions
Epremyan, K. K., Goleva, T. N., & Zvyagilskaya, R. A. (2022) · Biochemistry (Moscow) · doi:10.1134/s0006297922080028 · Cited by 11 · see citing works
Monocarboxylate Transporter 1 in Brain Diseases and Cancers
Sun, Y., Sun, J., He, Z., Wang, G., Wang, Y., Zhao, D., Wang, Z., Luo, C., Tian, C., & Jiang, Q. (2019) · Current Drug Metabolism · doi:10.2174/1389200220666191021103018 · Cited by 9 · see citing works
Self-citationYang, Y., Chen, R., Che, Y., Yao, X., Fang, M., Wang, Y., Zhou, D., Li, N., & Hou, Y. (2023) · Phytotherapy Research · doi:10.1002/ptr.7858 · Cited by 5 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 2
- [48]Gimeno-Bayon J, Lopez-Lopez A, Rodriguez MJ, Mahy N (2014). Glucose pathways adaptation supports acquisition of activated microglia phenotype. J Neurosci Res, 92: 723- 731. 24510633
- [125]Pan RY, He L, Zhang J, Liu X, Liao Y, Gao J, et al. (2022). Positive feedback regulation of microglial glucose metabolism by histone H4 lysine 12 lactylation in Alzheimer's disease. Cell Metab, 34: 634- 648.e636. 35303422
Cited by
Sorted by citations
Energy Metabolism and Brain Aging: Strategies to Delay Neuronal Degeneration
Na, D., Zhang, Z., Meng, M., Li, M., Gao, J., Kong, J., Zhang, G., & Guo, Y. (2025) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-025-01555-z · Cited by 42 · see citing works
He, C., Chen, B., Yang, H., & Zhou, X. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1554398 · Cited by 38 · see citing works
Wang, S., Wu, L., Xie, Y., Ge, S., Wu, Y., Chen, L., Yi, L., Yang, J., Duan, F., & Huang, L. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.118412 · Cited by 20 · see citing works
Dhiman, N., Deshwal, S., Rishi, V., Singhal, N. K., & Sandhir, R. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.115034 · Cited by 20 · see citing works
Glycolytic reprogramming during microglial polarization in neurological diseases
Li, X., Fang, C., Li, Y., Xiong, X., Xu, X., & Gu, L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1648887 · Cited by 23 · see citing works
Gao, R., Gao, Y., Su, W., & Wang, R. (2025) · Aging and Disease · doi:10.14336/ad.2024.1629 · Cited by 18 · see citing works
Microglial Neuroinflammation in Alzheimer’s Disease: Mechanisms and Therapies
Erdağ, E., & Haskologlu, I. C. (2025) · Journal of dementia and Alzheimer's disease · doi:10.3390/jdad2030029 · Cited by 20 · see citing works
Cheng, Y., Jung, J., Guo, L., Shuboni-Mulligan, D. D., Chen, J.-F., Hu, W., & Guo, M.-L. (2025) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2024.09.011 · Cited by 16 · see citing works
Spezani, R., & Mandarim‐de‐Lacerda, C. A. (2025) · Diabetes Obesity and Metabolism · doi:10.1111/dom.70400 · Cited by 19 · see citing works
Immunometabolism Reframes Alzheimer’s Disease: From Systemic Dysmetabolism to Glial Rewiring
Bach, D., & Nguyen, L. L. (2026) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-026-01691-0 · Cited by 13 · see citing works
Metabolic Flexibility of Microglia: Energy Substrate Utilization and Impact on Neuronal Metabolism
Westi, E. W., Carlsen, R. B., Andersen, J. V., Kilic, Z., Alnajar, D., Holmgaard, N. K., Sintes, B. G., Cota-Coronado, A., Muñoz, S. S., Galvagnion, C., et al. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70304 · Cited by 12 · see citing works
Bian, T., li, H., Liu, H., Guo, M., Zhang, Y., Hu, P., & Chen, M. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114279 · Cited by 10 · see citing works
Gao, X., Fu, S., Liu, Y., Yan, A., Sun, Y., Li, X., Liu, D., & He, D. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.04.049 · Cited by 9 · see citing works
Wu, C., Lin, J., Chen, Q., Zhao, W., Kawahata, K., & Cheng, A. (2025) · Cells · doi:10.3390/cells14191502 · Cited by 9 · see citing works
Saha, P., & Sharma, S. S. (2024) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.4c00329 · Cited by 8 · see citing works
Bridging the Gap: The Neuro-immune Axis as a Key Player in Neurodegenerative Disorders
Liu, T., Wu, H., & Wei, J. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01439-8 · Cited by 9 · see citing works
Neuroimmune Dysregulation and AI-Driven Therapeutic Strategies in Alzheimer’s Disease
Ghosh, S., Bhaskar, R., Singh, D. K. K., Sharma, S., Yarlagadda, B., Sinha, J. K., & Han, S. S. (2025) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-025-01651-0 · Cited by 10 · see citing works
Blood diagnostic and prognostic biomarkers in amyotrophic lateral sclerosis
Lv, Y.-T., & Li, H. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00286 · Cited by 8 · see citing works
Breaking Glycolysis Barriers to Immunotherapy with Nanomedicines
Zhang, M., Ren, Y., Li, J., Yu, J., Li, Q., Zhao, H., Wang, Z., Chen, X. S., & Cheng, J. (2025) · ACS Nano Medicine · doi:10.1021/acsnanomed.5c00042 · Cited by 9 · see citing works
Sugar Utilization by Microglia in Alzheimer's Disease
Marino, K. M., Shippy, D. C., & Ulland, T. K. (2024) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2025.578552 · Cited by 5 · see citing works
Benefits of virtual reality rehabilitation on neurodegenerative diseases: a systematic review
Tu, T., Yang, Y., Zheng, T., Lin, H., Wang, W., Fu, L., Jiang, S., & Wang, R. (2025) · npj Digital Medicine · doi:10.1038/s41746-025-02171-3 · Cited by 7 · see citing works
Fang, L., Zhuang, Y., Zhang, M., Yang, D., Zhang, R., Peng, J., & Wang, C. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1706597 · Cited by 5 · see citing works
RIPK1: A Promising Target for Intervention Neuroinflammation
Yan, F., Qiao, Y., Pan, S., Kang, A., Chen, H., & Bai, Y. (2025) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-025-10208-3 · Cited by 6 · see citing works
Viral reprogramming of glial metabolism as a driver of neuroinflammation
Rodrigues, T. S., Beltrão, G. S., Girardi, H., & Pinto, A. R. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1686774 · Cited by 5 · see citing works
Drug Screening and Validation Targeting TDP-43 Proteinopathy for Amyotrophic Lateral Sclerosis
Xin, J., Huang, S., Wen, J., Li, Y., Li, A., Satyanarayanan, S. K., Yao, X., & Su, H. (2024) · Aging and Disease · doi:10.14336/ad.2024.0440 · Cited by 4 · see citing works
Zhang, M., Ma, Z., Cui, H., Miao, Y., Yu, Y., Wen, Q., Liu, Z., Huang, X. H., Xing, C., Liu, K., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-96931-6 · Cited by 4 · see citing works
Yan, T., Kang, G., Meng, Y., Zhang, L., Jiang, Q. Y., Shen, N., Li, H., Xu, M., Yu, L., Ni, G., et al. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114945 · Cited by 3 · see citing works
Liu, M., Sun, Y. H., & Wu, J. S. (2025) · The International Journal of Psychiatry in Medicine · doi:10.1177/00912174251376110 · Cited by 3 · see citing works
Wu, Z., Yu, S., Tian, D., Li, C., & Jing, J. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1705069 · Cited by 3 · see citing works
Zhang, T., Wang, L., Ren, Z., Man, R., Cheng, X., Wang, L., Wang, J., Bu, X., & Yu, Y. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1853009 · Cited by 3 · see citing works
A mathematical model of microglia glucose metabolism and lactylation with positive feedback
Larripa, K., & Rǎdulescu, A. (2025) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2025.112049 · Cited by 2 · see citing works
Li, Z., Lin, Y. Y., Lu, Y., Zeng, L., Guan, H., Huang, F., Zeng, X., Yao, Q., & Zheng, R. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-08309-5 · Cited by 2 · see citing works
Zuo, J., Ding, R., Wang, X., Jing, G., Gong, H., Yuan, M., Xia, Y. F., Qin, J., Wu, X., & Song, X. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115417 · Cited by 2 · see citing works
Zhang, Y., Li, H., Yang, J., & Ma, H. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1602724 · Cited by 1 · see citing works
Li, Q., Liao, Y., Zhao, Y., Wu, H., Jin, T., Li, S., Liu, Y., Li, P., Ouyang, S., Li, Z., et al. (2026) · Advanced Science · doi:10.1002/advs.75125 · Cited by 1 · see citing works
The iron-energy metabolism axis in Alzheimer’s pathogenesis: from mechanisms to interventions
Zou, Z., Chen, J., Li, J., & Chen, Y.-F. (2026) · Cell Death Discovery · doi:10.1038/s41420-026-03034-w · Cited by 2 · see citing works
Glycolysis as a central pathological axis in neurodegenerative diseases
Cheng, T., Li, M., Yang, Y., Rao, Z., & Yang, W. (2026) · Reviews in the Neurosciences · doi:10.1515/revneuro-2026-0037 · Cited by 1 · see citing works
Huang, M., Qian, W., Lin, D., Zeng, Y., Zhou, Y., Zhang, S., 罗雅玲, Li, Z., & Du, X. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1821690 · Cited by 1 · see citing works
A Novel Approach to Neuropathic Pain Treatment: Lactylation Targeting Microglia
Chen, M., Yang, F., Sun, Y., & Feng, S. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05989-4 · Cited by 1 · see citing works
Glucose metabolic reprogramming: mechanisms and therapeutic implications in neuroinflammation
Zhang, L., Yang, X., & Ai, X. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1737175 · Cited by 1 · see citing works
Regenerative strategies for ALS: stem cells and extracellular vesicles
Raghunathan, T., Parthasarathy, B., Prabhu, P., Mahesh, P., & Dhanushkodi, A. (2026) · Discover Nano · doi:10.1186/s11671-026-04820-2 · Cited by 1 · see citing works
Cui, Q., Zheng, K., Liu, Q., Wang, L., Liu, Y., Bai, R., Zhang, W., Guo, J., Chang, X., & Wang, J. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1921079 · Cited by 1 · see citing works
HK2 drives synaptic dysfunction in fragile X syndrome via epigenetic regulation of H3K18 lactylation
Luan, Y., Zhang, H., Ma, N., Zhang, Y., Xu, Z., Zhang, W., Zhang, X., & Liu, Y. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1903604 · Cited by 1 · see citing works
Acupuncture Effect on Reaction-Time Changes in Parkinson’s Disease Patients—Case Study Series
Pereira, C. R., Greten, H. J., Santos, R. S., Reis, A. M., Ramos, B., Santos, M. J., Machado, J. P., & Criado, M. B. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13185642 · Cited by 1 · see citing works
Advancing Neurological Health: Insights into Aging, Immunity, and Vascular Dynamics
Xu, T., Ye, J., Gan, L., Deng, S., Guo, Y., & Tang, Y. (2024) · Aging and Disease · doi:10.14336/ad.2024.0423 · Cited by 1 · see citing works
Saleh, S. R., Atef, E., Maher, A. M., Ghareeb, D. A., Sheta, E., & Eweda, S. M. (2025) · Biological Trace Element Research · doi:10.1007/s12011-025-04764-1
Cañeque‐Rufo, H., Fontán‐Baselga, T., Rivera-Illades, E., Vicente‐Rodríguez, M., Gramage, E., Zapico, J. M., de Pascual‐Teresa, B., Ramos, P., & Herradón, G. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118671
Исаев, Н. К., Genrikhs, E. E., & Stelmashook, E. V. (2025) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-025-06521-9
Neurodegenerative Diseases and Glucose Metabolism of Neuroglial Cells
王, 书. (2026) · Advances in Clinical Medicine · doi:10.12677/acm.2026.162418
Zhao, R.-Y., Zhang, M., Wang, X.-W., Xue, F., Zheng, Y.-Y., & Chen, W.-F. (2026) · Inflammopharmacology · doi:10.1007/s10787-026-02160-2
Zafar, S., Rasheed, U., & Zerr, I. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1013648
Brogi, L., Fronte, B., Tonelli, F., Marchese, M., Cremisi, F., & Cellerino, A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.15.725450
Lima, M. N., Santos, L. F., Lemos, F. S., Reis, P. A., Maron‐Gutierrez, T., & Castro-Faria-Neto, H. C. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1663796
Wang, W., Wang, H., Zhou, C., & Fu, Y. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1830485
Neuroinflammation and Tauopathies
Zeenny, M.-N., Salame, I., Maatouk, L., & Akoury, E. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12253-4
Stelmashook, E. V., Genrikhs, E. E., Рафаилевна, К. М., Alexandrova, O. P., & Исаев, Н. К. (2026) · Biomeditsinskaya Khimiya · doi:10.18097/pbmcr1690
Chu, M., Tan, M., Gan, X., Cui, S., & Shi, L. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06091-5
Lv, C., Zhu, W., Wen, X., & Da, Y. (2026) · ASN NEURO · doi:10.1080/17590914.2026.2715625
SIRT1 deacetylates GAPDH to drive microglial glycolysis and neuroinflammation
Hsu, C., Sapaev, I., Nematov, O. N., Turakulov, R., abdullah, S. S., Khaleel, Z. T., Alwaily, E. R., & Jabir, M. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1883095
Zhao, Y., Linghu, T., Wang, Q., Gao, X., Qin, X., & Tian, J. (2026) · Analytical Chemistry · doi:10.1021/acs.analchem.6c00087
Neuroinflammation and metabolic reprogramming in Parkinson’s disease
Fu, Y., Yu, J., Xu, L., Zhou, T., & Deng, Q. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1857394
Abdel-Rasol, M. A. (2026) · Inflammopharmacology · doi:10.1007/s10787-026-02386-0
- Authors
- Huang, Q., Wang, Y., Chen, S., & Liang, F.
- Affiliations
- Central Hospital of Wuhan (CN)
- Venue
- Aging and disease
- Publisher
- Aging and Disease
- Published
- 2023
- Volume
- 15
- Issue
- 3
- Pages
- 0
- ISSN
- 2152-5250 (ISSN-L)
- PMC
- PMC11081147
- OpenAlex
- W4386037941
- Cited by
- 62
- References
- 175
- Citations by year
- 2026: 27 · 2025: 26 · 2024: 9
- FWCI
- 1.62
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Aging and Disease (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Hubei Province
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Keywords
- microglia, glucose metabolism, neuroinflammation, neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, microglial activation, metabolic reprogramming, therapeutic target
- MeSH terms
- Neuroinflammatory Diseases, Animals, Glucose, Humans, Microglia, Neurodegenerative Diseases
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