The DOI matches its Crossref record; 48 of the 50 references it cites were found in a registry or an index.
Protracted downregulation of CX3CR1 on microglia of aged mice after lipopolysaccharide challenge
Open accessAbstract
Fractalkine (CX(3)CL1) to fractalkine receptor (CX(3)CR1) interactions in the brain are involved in the modulation of microglial activation. Our recent findings indicate that there is microglial hyperactivity in the aged brain during an inflammatory challenge. The underlying cause of this amplified microglial response in the aged brain is unknown. Therefore, the purpose of this study was to determine the degree to which age-associated impairments of CX(3)CL1 and CX(3)CR1 in the brain contribute to exaggerated microglial activation after intraperitoneal (i.p.) injection of lipopolysaccharide (LPS). Here we show that CX(3)CL1 protein was reduced in the brain of aged (18-22 mo) BALB/c mice compared to adult (3-6 mo) controls. CX(3)CL1 protein, however, was unaltered by LPS injection. Next, CX(3)CR1 levels were determined in microglia (CD11b(+)/CD45(low)) isolated by Percoll density gradient separation at 4 and 24h after LPS injection. Flow cytometric and mRNA analyses of these microglia showed that LPS injection caused a marked decrease of CX(3)CR1 and a simultaneous increase of IL-1β at 4h after LPS injection. While surface expression of CX(3)CR1 was enhanced on microglia of adult mice by 24h, it was still significantly downregulated on a subset of microglia from aged mice. This protracted reduction of CX(3)CR1 corresponded with a delayed recovery from sickness behavior, prolonged IL-1β induction, and decreased TGFß expression in the aged brain. In the last set of studies BV2 microglia were used to determine effect of TGFß on CX(3)CR1. These results showed that TGFβ enhanced CX(3)CR1 expression and attenuated the LPS-induced increase in IL-1β expression.
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
“Aged glial cells respond less efficiently to antigens, including amyloid-β (Aβ) and α-synuclein, and have reduced phagocytic and antiinflammatory capacity (161–163).”
From Connecting aging biology and inflammation in the omics era (2022) · cites this paper as [163]
In the citing paper
“For example, if a microglial gene relevant to neurodegeneration at an early stage is to be investigated, it would be most appropriate to use a conditional and cell-specific model, such as the tamoxifen-inducible Cx3cr1 Cre recombinase mouse, since Cx3cr1 is only expressed by homeostatic microglia and is downregulated by DAM [66].”
From Identification and therapeutic modulation of a pro-inflammatory subset of disease-associated-microglia in Alzheimer’s disease (2018) · cites this paper as [66]
In the citing paper
“Furthermore, in vitro treatment of microglial cells with LPS followed by TGFβ significantly attenuated LPS-induced IL-1β expression (Wynne et al, 2010).”
From Microglia Priming with Aging and Stress (2017) · cites this paper as Wynne et al, 2010
In the citing paper
“Aged mice, but not adults, showed reduced baseline levels of CX 3 CL 1 that remained unaltered after a systemic LPS challenge (Wynne et al, 2010).”
From Microglia Priming with Aging and Stress (2017) · cites this paper as Wynne et al, 2010
In the citing paper
“LPS-injected aged mice, however, showed protracted downregulation of CX 3 CR 1 and reduced social behavior, which was accompanied by elevated IL-1β and reduced TGFβ (Wynne et al, 2010).”
From Microglia Priming with Aging and Stress (2017) · cites this paper as Wynne et al, 2010
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
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859
Resting 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
ATP mediates rapid microglial response to local brain injury in vivo
Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913
Control of microglial neurotoxicity by the fractalkine receptor
Cardona, A. E., Pioro, E. P., Sasse, M. E., Kostenko, V., Cardona, S. M., Dijkstra, I. M., Huang, D., Kidd, G., Dombrowski, S., Dutta, R., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1715 · Cited by 1,531
Harrison, J. K., Jiang, Y., Chen, S., Xia, Y., Maciejewski, D., McNamara, R. K., Streit, W. J., Salafranca, M. N., Adhikari, S., Thompson, D. A., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.18.10896 · Cited by 1,176
Godbout, J. P., Chen, J., Abraham, J., Richwine, A. F., Berg, B. M., Kelley, K. W., & Johnson, R. W. (2005) · The FASEB Journal · doi:10.1096/fj.05-3776fje · Cited by 813
Self-citationInnate immunity: the missing link in neuroprotection and neurodegeneration?
Nguyen, M. D., Julien, J., & Rivest, S. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn752 · Cited by 710
Microglia derived from aging mice exhibit an altered inflammatory profile
Sierra, A., Gottfried‐Blackmore, A. C., McEwen, B. S., & Bulloch, K. (2007) · Glia · doi:10.1002/glia.20468 · Cited by 688
Henry, C. J., Huang, Y., Wynne, A., Hanke, M., Himler, J., Bailey, M. T., Sheridan, J. F., & Godbout, J. P. (2008) · Journal of Neuroinflammation · doi:10.1186/1742-2094-5-15 · Cited by 678
Self-citationNeurotactin, a membrane-anchored chemokine upregulated in brain inflammation
Pan, Y., Lloyd, C. M., Zhou, H., Dolich, S., Deeds, J., Gonzalo, J.-Á., Vath, J., Gosselin, M., Ma, J., Dussault, B. J., et al. (1997) · Nature · doi:10.1038/42491 · Cited by 643
Flagged first, then by citations
2 of the 50 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 101–200 of 224
Glucocorticoid sensitization of microglia in a genetic mouse model of obesity and diabetes
Dey, A., Hao, S., Erion, J., Wosiski‐Kuhn, M., & Stranahan, A. M. (2014) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2014.01.013 · Cited by 60
Age-Dependent Changes in the Activation and Regulation of Microglia
Cornejo, F., & Rommy von Bernhardi, M. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-40764-7_10 · Cited by 61
Schreuder, L., Eggen, B. J. L., Biber, K. P. H., Schoemaker, R. G., Laman, J. D., & de Rooij, S. E. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.01.010 · Cited by 61
Aged Microglia in Neurodegenerative Diseases: Microglia Lifespan and Culture Methods
Yoo, H.-J., & Kwon, M. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.766267 · Cited by 65
Lv, B., Huo, F., Zhu, Z., Xu, Z., Xiaojie, D., Chen, T., Zhang, T., & Yang, X. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1905-1 · Cited by 59
Microglial Priming in Infections and Its Risk to Neurodegenerative Diseases
Lima, M. N., Barbosa‐Silva, M. C., & Maron‐Gutierrez, T. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.878987 · Cited by 66
Role of cytokines and reactive oxygen species in brain aging
MohanKumar, S. M. J., Murugan, A., Palaniyappan, A., & MohanKumar, P. S. (2023) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2023.111855 · Cited by 59
Lieblein‐Boff, J. C., McKim, D. B., Shea, D. T., Wei, P. Y., Deng, Z., Sawicki, C. M., Quan, N., Bilbo, S. D., Bailey, M. T., McTigue, D. M., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0708-13.2013 · Cited by 57
Self-citationO’Neil, S. M., Hans, E., Jiang, S., Wangler, L. M., & Godbout, J. P. (2022) · Glia · doi:10.1002/glia.24147 · Cited by 60
Self-citationSutherland, T. C., & Geoffroy, C. G. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00190 · Cited by 56
Bardou, I., Kaercher, R. M., Brothers, H. M., Hopp, S. C., Royer, S. E., & Wenk, G. L. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.11.006 · Cited by 56
Trojan, E., Ślusarczyk, J., Chamera, K., Kotarska, K., Głombik, K., Kubera, M., & Basta‐Kaim, A. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00779 · Cited by 54
Effects of voluntary wheel running on LPS-induced sickness behavior in aged mice
Martin, S. A., Pence, B. D., Greene, R. M., Johnson, S. J., Dantzer, R., Kelley, K. W., & Woods, J. A. (2012) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2012.12.014 · Cited by 52
Wang, L., Liu, Y., Yan, S., Du, T., Fu, X., Gong, X., Zhou, X., Zhang, T., & Wang, X. (2020) · Aging and disease · doi:10.14336/ad.2019.0615 · Cited by 49
Kelley, K. W., O’Connor, J. C., Lawson, M. A., Dantzer, R., Rodriguez-Zas, S. L., & McCusker, R. H. (2013) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2013.02.003 · Cited by 49
Fractalkine/CX3CR1-Dependent Modulation of Synaptic and Network Plasticity in Health and Disease
Camacho-Hernández, N. P., & Peña‐Ortega, F. (2023) · Neural Plasticity · doi:10.1155/2023/4637073 · Cited by 52
Bronzuoli, M. R., Facchinetti, R., Valenza, M., Cassano, T., Steardo, L., & Scuderi, C. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00644 · Cited by 48
Immunity and Alzheimer's disease: immunological perspectives on the development of novel therapies
Liu, Y.-H., Zeng, F., Wang, Y., Zhou, H., Giunta, B. N., Tan, J., & Wang, Y. (2013) · Drug Discovery Today · doi:10.1016/j.drudis.2013.07.020 · Cited by 48
Basic Aspects of the Immunology of Neuroinflammation
Wohleb, E. S., & Godbout, J. P. (2013) · Modern trends in psychiatry · doi:10.1159/000343964 · Cited by 49
Self-citationImmunoreactive Cells After Cerebral Ischemia
Wang, Y., Zhang, J. H., Sheng, J., & Shao, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02781 · Cited by 45
Microglial CX3CR1 production increases in Alzheimer's disease and is regulated by noradrenaline
González‐Prieto, M., Gutiérrez, I. L., García‐Bueno, B., Caso, J. R., Leza, J. C., Ortega‐Hernández, A., Gómez‐Garré, D., & Madrigal, J. L. M. (2020) · Glia · doi:10.1002/glia.23885 · Cited by 42
Perkins, A. E., Piazza, M. K., & Deak, T. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.02.028 · Cited by 43
Microglia and Brain Disorders: The Role of Vitamin D and Its Receptor
Mirarchi, A., Albi, E., Beccari, T., & Arcuri, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241511892 · Cited by 47
Macrophages make me sick: How macrophage activation states influence sickness behavior
Moon, M. L., McNeil, L. K., & Freund, G. G. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.07.002 · Cited by 40
Pandur, E., Tamási, K., Pap, R., Varga, E., Miseta, A., & Sipos, K. (2019) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-019-00694-4 · Cited by 37
de Sousa, V. L., Araújo, S. M. B., Antônio, L. M. D. S., Silva-Queiroz, M., Colodeti, L. C., Soares, C., Barros‐Aragão, F. G. Q., Mota-Araujo, H. P., Alves, V. S., Coutinho‐Silva, R., et al. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.04.001 · Cited by 38
Atkinson, J., Jerome, A. D., Sas, A., Munie, A. N., Wang, C., Ma, A., Arnold, W. D., & Segal, B. M. (2022) · JCI Insight · doi:10.1172/jci.insight.158153 · Cited by 36
HIV-1 Tat Disrupts CX3CL1-CX3CR1 Axis in Microglia via the NF-κBYY1 Pathway
Duan, M., Yao, H., Cai, Y. C., Liao, K., Seth, P., & Buch, S. J. (2014) · Current HIV Research · doi:10.2174/1570162x12666140526123119 · Cited by 34
Sarma, J. D., Burrows, A. C., Rayman, P. A., Hwang, M., Kundu, S., Sharma, N., Bergmann, C. C., & Sen, G. C. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1009034 · Cited by 34
Chamera, K., Szuster-Głuszczak, M., Trojan, E., & Basta-Kaim, A. (2020) · Cells · doi:10.3390/cells9071676 · Cited by 31
Martin, S. A., Dantzer, R., Kelley, K. W., & Woods, J. A. (2013) · NeuroImmunoModulation · doi:10.1159/000356144 · Cited by 32
Aurelian, L., & Balan, I. S. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05220-4 · Cited by 31
Sanchez-Molina, P., Almolda, B., Giménez‐Llort, L., González, B., & Castellano, B. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.12.026 · Cited by 32
The effect of CX3CL1/ CX3CR1 signal axis on microglia in central nervous system diseases
Zhao, J., Li, Q., Ouyang, X., Wang, F., Li, Q., Xu, Z., Ji, D., Wu, Q., Zhang, J., Lu, C., et al. (2023) · Journal of Neurorestoratology · doi:10.1016/j.jnrt.2023.100042 · Cited by 29
The age-related microglial transformation in Alzheimer's disease pathogenesis
Yuan, C., Aierken, A., Xie, Z., Li, N., Zhao, J., & Qing, H. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.03.024 · Cited by 27
Postoperative Delirium in Neurosurgical Patients: Recent Insights into the Pathogenesis
Xu, Y., Ma, Q., Du, H., Yang, C., & Lin, G. (2022) · Brain Sciences · doi:10.3390/brainsci12101371 · Cited by 28
Zhu, Y., Li, L., Jin, X., Li, Z., Wang, C., Teng, L., Li, Y., Zhang, Y., & Wang, D. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.128819 · Cited by 29
Townsend, B. E., Chen, Y.-J., Jeffery, E. H., & Johnson, R. W. (2014) · Nutrition Research · doi:10.1016/j.nutres.2014.10.001 · Cited by 27
Yamanashi, T., Malicoat, J. R., Steffen, K. T., Zarei, K., Li, R., Purnell, B. S., Najafi, A., Saito, K., Singh, U., Toth, B. A., et al. (2020) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2020.12.036 · Cited by 28
Kwon, J., Suessmilch, M., McColl, A., Cavanagh, J., & MORRIS, B. J. (2021) · Scientific Reports · doi:10.1038/s41598-021-03216-9 · Cited by 26
Aging reduces glial uptake and promotes extracellular accumulation of Aβ from a lentiviral vector
Zhao, W., Zhang, J., Davis, E. G., & Rebeck, G. W. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00210 · Cited by 24
Chamera, K., Trojan, E., Kotarska, K., Szuster-Głuszczak, M., Bryniarska, N., Tylek, K., & Basta‐Kaim, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041558 · Cited by 25
Mao, L., You, J., Xie, M., Hu, Y., & Zhou, Q. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04019-5 · Cited by 27
Bemiller, S. M., Maphis, N. M., Formica, S. V., Wilson, G. N., Miller, C. M., Xu, G., Kokiko-Cochran, O. N., Kim, K.-W., Jung, S., Cannon, J. L., et al. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1310-6 · Cited by 24
Differential response to intrahippocampal interleukin-4/interleukin-13 in aged and exercise mice
Littlefield, A. M., & Kohman, R. A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.027 · Cited by 24
Microglia-astrocyte crosstalk following ischemic stroke
Yang, S., Chen, Y., Tang, J., Cui, Y., Wei, W., Hao, Z., Xiao, Z., Pan, Y., Tian, Q., Xin, W., et al. (2025) · Molecular Brain · doi:10.1186/s13041-025-01244-4 · Cited by 29
Brain sex-dependent alterations after prolonged high fat diet exposure in mice
Murtaj, V., Penati, S., Belloli, S., Foti, M., Coliva, A., Papagna, A., Gotti, C., Toninelli, E., Chiaffarelli, R., Mantero, S., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-04214-x · Cited by 26
Aging Microglia: Relevance to Cognition and Neural Plasticity
Kohman, R. A. (2012) · Methods in molecular biology · doi:10.1007/978-1-62703-071-7_11 · Cited by 25
Modulation of inflammatory responses by fractalkine signaling in microglia
Inoue, K., Morimoto, H., Ohgidani, M., & Ueki, T. (2021) · PLOS ONE · doi:10.1371/journal.pone.0252118 · Cited by 22
Tristão, F. S. M., Lazzarini, M., Martin, S., Amar, M., Stühmer, W., Kirchhoff, F., Gomes, L. C., Lanfumey, L., Prediger, R. D., Sepulveda-Diaz, J. E., et al. (2015) · Neurotoxicity Research · doi:10.1007/s12640-015-9557-5 · Cited by 22
Perkins, A. E., Varlinskaya, E. I., & Deak, T. (2019) · International review of neurobiology · doi:10.1016/bs.irn.2019.08.001 · Cited by 23
Immunomodulators as Therapeutic Agents in Mitigating the Progression of Parkinson’s Disease
Grimmig, B., Morganti, J., Nash, K., & Bickford, P. (2016) · Brain Sciences · doi:10.3390/brainsci6040041 · Cited by 17
Loss of NF-κB p50 function synergistically augments microglial priming in the middle-aged brain
Taetzsch, T., Benusa, S. D., Levesque, S., Mumaw, C. L., & Block, M. L. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1446-z · Cited by 21
The Role of Microglial CX3CR1 in Schizophrenia-Related Behaviors Induced by Social Isolation
Zhou, H., Wang, J., Zhang, Y., Shao, F., & Wang, W. (2020) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2020.551676 · Cited by 21
Littrell, J. L. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00297 · Cited by 22
Cohen, E. M., Mohammed, S., Kavurma, M. M., Nedoboy, P. E., Cartland, S. P., Farnham, M. M. J., & Pilowsky, P. M. (2018) · Autonomic Neuroscience · doi:10.1016/j.autneu.2018.12.002 · Cited by 20
Age and sex differences in primary microglia culture: A comparative study
Ngwa, C., Qi, S., Mamun, A. A., Xu, Y., Sharmeen, R., & Liu, F. (2021) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2021.109359 · Cited by 22
Navarro, E., Norden, D. M., Trojanowski, P. J., Godbout, J. P., & López, M. G. (2021) · Molecules · doi:10.3390/molecules26082107 · Cited by 20
Self-citationImplications for microglial sex differences in tau-related neurodegenerative diseases
Doust, Y. V., King, A. E., & Ziebell, J. M. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.03.010 · Cited by 18
Ayilara, G. O., & Owoyele, B. V. (2023) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2023.05.010 · Cited by 18
Age-dependent changes on fractalkine forms and their contribution to neurodegenerative diseases
Eugenín, J. L., Bernhardi, L. E.-V., & Rommy von Bernhardi, M. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1249320 · Cited by 19
Brito, H. O., Radulski, D. R., Wilhelms, D., Stojakovic, A., Brito, L. M. O., Engblom, D., Franco, C. R. C., & Zampronio, A. R. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12414 · Cited by 18
Microglia in Brain Aging and Age-Related Diseases: Friends or Foes?
Ishikawa, K., Fujikawa, R., Okita, K., Kimura, F., Watanabe, T., Katsurabayashi, S., & Iwasaki, K. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311494 · Cited by 18
Fractalkine Attenuates Microglial Cell Activation Induced by Prenatal Stress
Ślusarczyk, J., Trojan, E., Głombik, K., Chamera, K., Roman, A., Budziszewska, B., & Basta‐Kaim, A. (2016) · Neural Plasticity · doi:10.1155/2016/7258201 · Cited by 17
RetractedNeuronal-Glial Mechanisms of Exercise-Evoked Stress Robustness
Fleshner, M., Greenwood, B. N., & Yirmiya, R. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_277 · Cited by 16
Quantitative, structural and molecular changes in neuroglia of aging mammals: A review
Pannese, E. (2021) · European Journal of Histochemistry · doi:10.4081/ejh.2021.3249 · Cited by 16
Nheu, D., Ellen, O., Ye, S., Öztürk, E., Pagnin, M., Kertadjaja, S., Theotokis, P., Grigoriadis, N., McLean, C., & Petratos, S. (2022) · Cells · doi:10.3390/cells11233768 · Cited by 16
Li, Z., Cao, X., Ma, H., Cui, Y., Li, X., Wang, N., & Zhou, Y. (2018) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nly051 · Cited by 15
Cannella, L. A., Andrews, A. M., Tran, F. H., Razmpour, R., McGary, H. M., Collie, C., Tsegaye, T., Maynard, M., Kaufman, M. J., Rawls, S. M., et al. (2019) · Journal of Neurotrauma · doi:10.1089/neu.2019.6472 · Cited by 18
Taipa, R. J. F., Sousa, A. L., Pires, M. M., & Sousa, N. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-160121 · Cited by 15
Pancreatic Stellate Cells and CX3CR1
Uchida, M., Ito, T., Nakamura, T., Hijioka, M., Igarashi, H., Oono, T., Kato, M., Nakamura, K., Suzuki, K., Takayanagi, R., et al. (2014) · Pancreas · doi:10.1097/mpa.0000000000000109 · Cited by 14
Iankov, I. D., Penheiter, A. R., Griesmann, G. E., Carlson, S. K., Federspiel, M. J., & Galanis, E. (2012) · Virus Research · doi:10.1016/j.virusres.2012.12.002 · Cited by 14
Chemokine CX3CL1 (Fractalkine) Signaling and Diabetic Encephalopathy
Wątroba, M., Grabowska, A. D., & Szukiewicz, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147527 · Cited by 13
Ageing-related changes in the regulation of microglia and their interaction with neurons
Rommy von Bernhardi, M., & Eugenín, J. L. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110241 · Cited by 10
Potential significance of CX3CR1 dynamics in stress resilience against neuronal disorders
Inoue, K. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.335831 · Cited by 10
Chemically Induced Senescence Prompts Functional Changes in Human Microglia‐Like Cells
Armanville, S., Tocco, C., Mohamad, Z., Clarke, D., Robitaille, R., & Drouin‐Ouellet, J. (2025) · Journal of Immunology Research · doi:10.1155/jimr/3214633 · Cited by 9
Cell ageing: a flourishing field for neurodegenerative diseases
Brites, D. M. T. O. (2015) · AIMS molecular science · doi:10.3934/molsci.2015.3.225 · Cited by 10
Capriotti, Z., & Klase, Z. A. (2024) · Journal of NeuroVirology · doi:10.1007/s13365-024-01239-2 · Cited by 11
Suryawanshi, Y. R., Nace, R. A., Russell, S. J., & Schulze, A. J. (2021) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2021.08.011 · Cited by 8
Stojić-Vukanić, Z., Pilipović, I., Djikić, J., Vujnović, I., Nacka-Aleksić, M., Bufan, B., Arsenović-Ranin, N., Kosec, D. J., & Leposavić, G. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.11.002 · Cited by 9
Sex as a determinant of age-related changes in rat spinal cord inflammation-oxidation state
Nacka-Aleksić, M., Stojanović, M., Simic, L., Bufan, B., Kotur‐Stevuljević, J., Stojić-Vukanić, Z., Dimitrijević, M., Ražić, S., & Leposavić, G. (2017) · Biogerontology · doi:10.1007/s10522-017-9726-4 · Cited by 9
Advances in the multifunctional roles of CX3CL1 in the central nervous system
Chen, Y., Liu, J., Zhang, S., Gao, M., Wang, F., Cai, M., Lu, C., Li, S. A., & Zhao, J. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2026.1696689 · Cited by 7
Timmerman, R., Zuiderwijk-Sick, E. A., Oosterhof, N., Jong, A. E. J. '., Veth, J., Burm, S. M., van Ham, T. J., & Bajramovic, J. J. (2021) · Glia · doi:10.1002/glia.24136 · Cited by 6
Balan, I. S., Grusca, A., Chéry, S. L., Materia, B. R., O’Buckley, T. K., & Morrow, A. L. (2024) · Life · doi:10.3390/life14070860 · Cited by 6
Lucassen, P., van Dam, A., Kandel, P., Bielefeld, P., Korosi, A., Fitzsimons, C., & Maletić-Savatić, M. (2019) · Health Psychology and Behavioral Medicine · doi:10.1042/ns20180208 · Cited by 5
Watters, J. J., & Pocock, J. M. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1429-6_3 · Cited by 5
Mammary tumors suppress aging-induced neuroinflammation in female Balb/c mice
Barrientos, R. M., Strehle, L. D., Lahoud, A. A., & Pyter, L. M. (2020) · Comprehensive Psychoneuroendocrinology · doi:10.1016/j.cpnec.2020.100002 · Cited by 5
Age-Dependent Microglial Response to Systemic Infection
Cyr, B. S., & Vaccari, J. P. D. R. (2021) · Cells · doi:10.3390/cells10051037 · Cited by 5
Neuroinflammation in Dementia—Therapeutic Directions in a COVID-19 Pandemic Setting
Łuc, M., Woźniak, M., & Rymaszewska, J. (2022) · Cells · doi:10.3390/cells11192959 · Cited by 4
Aging Microglia and Their Impact in the Nervous System
Rommy von Bernhardi, M., & Eugenín, J. L. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-55529-9_21 · Cited by 4
Effects of age on retinal macrophage responses to acute elevation of intraocular pressure
Kezic, J. M., Chrysostomou, V., McMenamin, P. G., & Crowston, J. G. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.107995 · Cited by 3
Fenn, A. M., Corona, A. W., & Godbout, J. P. (2013) · Wiley eBooks · doi:10.1002/9781118314814.ch16 · Cited by 4
Self-citationSuccinum extracts inhibit microglial-derived neuroinflammation and depressive-like behaviors
Kang, J.-Y., Baek, D.-C., Son, C., & Lee, J. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.991243 · Cited by 3
Epigenetic mechanisms of inflammatory memory in the central nervous system
Ye, J. J., & Quintana, F. J. (2026) · Nature Immunology · doi:10.1038/s41590-026-02541-3 · Cited by 3
Animal Models to Study the Role of Kynurenine Pathway in Mood, Behavior, and Cognition
Castanon, N. (2015) · Springer eBooks · doi:10.1007/978-3-319-11870-3_25 · Cited by 2
Valiati, F. E., Hizo, G. H., Pinto, J. V., & Kauer‐Sant’Anna, M. (2019) · Current Psychiatry Research and Reviews · doi:10.2174/1573400515666190719155906 · Cited by 1
The Effect of Systemic Inflammation on Cognitive Function and Neurodegenerative Disease
Cunningham, C. M., & Skelly, D. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108539623.010 · Cited by 1
Microglial Biology and Physiology
Butovsky, O., Madore, C., & Weiner, H. L. (2016) · Springer eBooks · doi:10.1007/978-3-319-44022-4_13 · Cited by 1
Stojić-Vukanić, Z., Pilipović, I., Arsenović-Ranin, N., Dimitrijević, M., & Leposavić, G. (2021) · Immunology Letters · doi:10.1016/j.imlet.2021.08.003 · Cited by 1
Fenn, A. M., Norden, D. M., & Godbout, J. P. (2015) · Wiley eBooks · doi:10.1002/9781118732748.ch6 · Cited by 1
Self-citation
Metadata
- Authors
- Wynne, A. M., Henry, C. J., Huang, Y., Cleland, A., & Godbout, J. P.
- Affiliations
- The Ohio State University (US)
- Corresponding author
- Godbout, Jonathan P.
- Venue
- Brain, Behavior, and Immunity
- Publisher
- Elsevier BV
- Published
- 2010-10
- Volume
- 24
- Issue
- 7
- Pages
- 1190-1201
- ISSN
- 0889-1591 (ISSN-L)
- PMC
- PMC2939290
- OpenAlex
- W2087771052
- Cited by
- 224
- References
- 50
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 8 · 2023: 9 · 2022: 17 · 2021: 19 · 2020: 14 · 2019: 13 · 2018: 18 · 2017: 10 · 2016: 18 · 2015: 17 · 2014: 21 · 2013: 18 · 2012: 15
- FWCI
- 9.68
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Brain Behavior and Immunity (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (R01AG033028, R01 AG-033028-01)
- National Institute of Mental Health (R21MH077817)
- National Institute of Allergy and Infectious Diseases (NIH T32-AI-055411, T32AI055411)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
- Keywords
- CX3CR1, fractalkine, microglia, aging, lipopolysaccharide, neuroinflammation, microglial activation, IL-1β, TGF-beta, sickness behavior, BV-2 cells, aged mice
- MeSH terms
- CX3C Chemokine Receptor 1, Aging, Animals, Brain, Cell Count, Cells, Cultured, Enzyme-Linked Immunosorbent Assay, Flow Cytometry, Injections, Intraperitoneal, Lipopolysaccharides, Male, Mice, Inbred BALB C, RNA, Messenger, Down-Regulation, Up-Regulation, Polymerase Chain Reaction, Transforming Growth Factor beta, Leukocyte Common Antigens, Microglia, Receptors, Chemokine, CD11b Antigen, Mice, Interleukin-1beta, Chemokine CX3CL1
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