MICROGLIA AS MEDIATORS OF INFLAMMATORY AND DEGENERATIVE DISEASES

Rapid turnover of plasma virions and CD4 lymphocytes in HIV-1 infection

Ho, D. D., Neumann, A. U., Perelson, A. S., Chen, W., Leonard, J. M., & Markowitz, M. H. (1995) · Nature · doi:10.1038/373123a0 · Cited by 4,261

HIV-1 Entry Cofactor: Functional cDNA Cloning of a Seven-Transmembrane, G Protein-Coupled Receptor

Feng, Y. Y., Broder, C. C., Kennedy, P. E., & Berger, E. A. (1996) · Science · doi:10.1126/science.272.5263.872 · Cited by 4,169

Axonal transection in the lesions of multiple sclerosis

Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029

HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5

Dragic, T., Litwin, V., Allaway, G. P., Martin, S. R., Huang, Y., Nagashima, K. A., Cayanan, C. S., Maddon, P. J., Koup, R. A., Moore, J. P., et al. (1996) · Nature · doi:10.1038/381667a0 · Cited by 3,173

Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development

Zou, Y.-R., Kottmann, A. H., Kuroda, M., Taniuchi, I., & Littman, D. R. (1998) · Nature · doi:10.1038/31269 · Cited by 2,531

A Dual-Tropic Primary HIV-1 Isolate That Uses Fusin and the β-Chemokine Receptors CKR-5, CKR-3, and CKR-2b as Fusion Cofactors

Doranz, B. J., Rucker, J. B., Yi, Y., Smyth, R. J., Samson, M., Peiper, S. C., Parmentier, M., Collman, R. G., & Doms, R. W. (1996) · Cell · doi:10.1016/s0092-8674(00)81314-8 · Cited by 1,833

Arthritis and anti-inflammatory agents as possible protective factors for Alzheimer's disease: A review of 17 epidemiologic studies

McGeer, P. L., Schulzer, M., & McGeer, E. G. (1996) · Neurology · doi:10.1212/wnl.47.2.425 · Cited by 1,367

Activation of microglial cells by β-amyloid protein and interferon-γ

Meda, L., Cassatella, M. A., Szendrei, G. I., Otvos, L., Baron, P., Villalba, M., Ferrari, D., & Rossi, F. (1995) · Nature · doi:10.1038/374647a0 · Cited by 1,314

Cellular localization of human immunodeficiency virus infection within the brains of acquired immune deficiency syndrome patients.

Wiley, C. A., Schrier, R. D., Nelson, J. A., Lampert, P. W., & Oldstone, M. B. A. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.18.7089 · Cited by 1,242

Cytotoxicity of microglia

Banati, R. B., Gehrmann, J., Schubert, P., & Kreutzberg, G. W. (1993) · Glia · doi:10.1002/glia.440070117 · Cited by 1,032

Hispidin inhibits LPS‑induced nitric oxide production in BV‑2 microglial cells via ROS‑dependent MAPK signaling

Jin, M., Chen, D., Jin, Y.-H., Han, Y., Sun, H., & Kwon, T. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.10402 · Cited by 17

Toxicity of CSF in motor neurone disease: a potential route to neuroprotection

Shaw, P. J. (2002) · Brain · doi:10.1093/brain/awf138 · Cited by 17

Characterization of Amyloid-β Plaques and Autofluorescent Lipofuscin Aggregates in Alzheimer’s Disease Brain: A Confocal Microscopy Approach

Kun, A., González‐Camacho, F., Hernandez, S. F., Moreno-García, A., Calero, O., & Calero, M. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7816-8_31 · Cited by 17

Dcf1 Deficiency Attenuates the Role of Activated Microglia During Neuroinflammation

Wang, J., Li, J., Wang, Q., Kong, Y., Zhou, F., Li, Q., Li, W., Sun, Y., Wang, Y., Guan, Y., et al. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00256 · Cited by 18

Effects of Memantine in a Mouse Model of Postoperative Cognitive Dysfunction

Almahozi, A., Radhi, M. A., Alzayer, S., & Kamal, A. (2019) · Behavioral Sciences · doi:10.3390/bs9030024 · Cited by 17

The Messenger Apps of the cell: Extracellular Vesicles as Regulatory Messengers of Microglial Function in the CNS

Olanrewaju, A. A., & Hakami, R. M. (2020) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-020-09916-9 · Cited by 17

Human immunodeficiency virus type 1 envelope-mediated neuropathogenesis: targeted gene delivery by a Sindbis virus expression vector

van Marle, G., Ethier, J., Silva, C., MacVicar, B. A., & Power, C. (2003) · Virology · doi:10.1016/s0042-6822(02)00139-3 · Cited by 17

Selective modulation of microglial signal transduction by PACAP

Lee, H., & Suk, K. (2004) · Neuroreport · doi:10.1097/01.wnr.0000130541.29635.6f · Cited by 17

The Reactive Astrocyte

Norenberg, M. D. (2004) · CRC Press eBooks · doi:10.1201/9781420039740.ch5 · Cited by 17

HIV and FIV glycoproteins increase cellular tau pathology via cGMP-dependent kinase II activation

Sathler, M. F., Doolittle, M. J., Cockrell, J. A., Nadalin, I. R., Hofmann, F. B., VandeWoude, S., & Kim, S. (2022) · Journal of Cell Science · doi:10.1242/jcs.259764 · Cited by 18

Chronic exposure to l-BMAA cyanotoxin induces cytoplasmic TDP-43 accumulation and glial activation, reproducing an amyotrophic lateral sclerosis-like phenotype in mice

Anzilotti, S., Valente, V., Brancaccio, P., Franco, C., Casamassa, A., Lombardi, G., Palazzi, A., Conte, A., Paladino, S., Canzoniero, L. M. T., et al. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115503 · Cited by 16

Anesthesia-mediated neuroinflammatory sequelae in post operative cognitive dysfunction: mechanisms and therapeutic implications

Smith, G. T., Chen, T. J., Shah, N. M., Agrest, B., & Grotticelli, J. (2024) · Frontiers in Anesthesiology · doi:10.3389/fanes.2024.1281034 · Cited by 17

Shikonin Isolated from Lithospermum erythrorhizon Downregulates Proinflammatory Mediators in Lipopolysaccharide-Stimulated BV2 Microglial Cells by Suppressing Crosstalk between Reactive Oxygen Species and NF-κB

Prasad, R. G., Choi, Y. H., & Kim, G. (2015) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2015.006 · Cited by 16

Sauchinone suppresses lipopolysaccharide-induced inflammatory responses through Akt signaling in BV2 cells

Jang, E. Y., Yang, C. H., Han, M. H., Choi, Y. H., & Hwang, M. (2012) · International Immunopharmacology · doi:10.1016/j.intimp.2012.07.002 · Cited by 16

Ionizing radiation induced long-term alterations in the adult rat rostral migratory stream

Bálentová, S., Hajtmanová, E., Trylčová, R., Adamkov, M., & Lehotský, J. (2013) · Acta Histochemica · doi:10.1016/j.acthis.2013.08.002 · Cited by 16

Structure–activity relationships of novel iodinated quinoline-2-carboxamides for targeting the translocator protein

Blair, A., Stevenson, L., Dewar, D., Pimlott, S. L., & Sutherland, A. J. (2013) · MedChemComm · doi:10.1039/c3md00249g · Cited by 17

Propofol partially attenuates complete freund's adjuvant‐induced neuroinflammation through inhibition of the ERK1/2/NF‐κB pathway

Cheng, L., Chen, Z., Wang, L., Lan, Y., Zheng, L., & Wu, F. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28215 · Cited by 16

Anti-Inflammatory Effect of Wasp Venom in BV-2 Microglial Cells in Comparison with Bee Venom

Yun, H. S., Oh, J., Lim, J. S., Kim, H. J., & Kim, J. (2021) · Insects · doi:10.3390/insects12040297 · Cited by 17

Prostaglandin E2 Reverses Aberrant Production of an Inflammatory Chemokine by Microglia from Sandhoff Disease Model Mice through the cAMP-PKA Pathway

Kawashita, E., Tsuji, D., Toyoshima, M., Kanno, Y., Matsuno, H., & Itoh, K. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016269 · Cited by 16

Vasoactive intestinal peptide family as a therapeutic target for Parkinson’s disease

González‐Rey, E., Chorny, A., Fernandez‐Martin, A., Varela, N., & Delgado, M. (2005) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.9.5.923 · Cited by 16

Real-Time Detection of Reactive Oxygen Intermediates From Single Microglial Cells

Twig, G., Jung, S., Messerli, M. A., Smith, P. J., & Shirihai, O. S. (2001) · Biological Bulletin · doi:10.2307/1543355 · Cited by 16

Signaling Mechanisms Underlying Toxicant-Induced Gliosis

O'Callaghan, J. P., & Sriram, K. (2004) · CRC Press eBooks · doi:10.1201/9781420039740.ch9 · Cited by 17

Interrelations between nuclear-factor kappa B activation, glial response and neuronal apoptosis in gerbil hippocampus after ischemia

Domańska‐Janik, K., Bronisz, A., Zajac, H., & Zabłocka, B. (2001) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2001-1383 · Cited by 16

Nigella sativa Oil Reduces LPS-Induced Microglial Inflammation: An Evaluation on M1/M2 Balance

Hosseini, A., Rahimi, V. B., Rakhshandeh, H., & Askari, V. R. (2022) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2022/5639226 · Cited by 15

HIV induces synaptic hyperexcitation via cGMP-dependent protein kinase II activation in the FIV infection model

Sztukowski, K., Nip, K., Ostwald, P., Sathler, M. F., Sun, J. L., Shou, J., Jorgensen, E. T., Brown, T. E., Elder, J. H., Miller, C., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005315 · Cited by 17

MERS-CoV infection causes brain damage in human DPP4-transgenic mice through complement-mediated inflammation

Jiang, Y., Chen, Y., Sun, H. C., Zhang, X., He, L., Li, J., Zhao, G., & Sun, S. (2021) · Journal of General Virology · doi:10.1099/jgv.0.001667 · Cited by 15

A comparative study of cells in inflammation, EAE and MS using biomedical literature data mining

Palakal, M. J., Bright, J. J., Sebastian, T. B., & Hartanto, S. (2006) · Journal of Biomedical Science · doi:10.1007/s11373-006-9120-8 · Cited by 15

Intracellular Ion Channel CLIC1: Involvement in Microglia-Mediated β-Amyloid Peptide(1-42) Neurotoxicity

Skaper, S. D., Facci, L., & Giusti, P. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1084-2 · Cited by 16

Temporal transcriptomic profiling reveals cellular targets that govern survival in HOCl-mediated neuronal apoptosis

Yap, Y. W., Chen, M. J., Choy, M. S., Peng, Z. F., Whiteman, M., Manikandan, J., Melendez, A. J., & Cheung, N. S. (2010) · Life Sciences · doi:10.1016/j.lfs.2010.08.011 · Cited by 15

Myelin genes are downregulated in canine fucosidosis

Fletcher, J. L., Kondagari, G. S., Wright, A. L., Thomson, P. C., Williamson, P., & Taylor, R. M. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.06.001 · Cited by 15

Rapid and efficient radiosynthesis of [123I]I-PK11195, a single photon emission computed tomography tracer for peripheral benzodiazepine receptors

Pimlott, S. L., Stevenson, L. M., Wyper, D. J., & Sutherland, A. J. (2008) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2008.02.013 · Cited by 15

Gamma-decanolactone inhibits iNOS and TNF-alpha production by lipopolysaccharide-activated microglia in N9 cells

Pflüger, P., Viau, C. M., Coelho, V. R., Berwig, N. A., Staub, R. B., Pereira, P., & Saffi, J. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.03.029 · Cited by 15

Triterpenoid saponins and phenylpropanoid glycosides from the roots of Polygala japonica Houtt. with anti-inflammatory activity

Quang, T. H., Công, P. T., Yến, D. T. H., Nhiệm, N. X., Tài, B. H., Yến, P. H., Ngân, N. T. T., Kim, D. C., Kim, Y., Oh, H., et al. (2018) · Phytochemistry Letters · doi:10.1016/j.phytol.2018.01.008 · Cited by 15

Novel apoE receptor mimetics reduce LPS-induced microglial inflammation.

(2019) · Europe PMC (PubMed Central) · Cited by 15

The lack of Pneumococcal surface protein C (PspC) increases the susceptibility of Streptococcus pneumoniae to the killing by microglia

Peppoloni, S., Colombari, B., Neglia, R. G., Quaglino, D., Iannelli, F., Oggioni, M. R., Pozzi, G., & Blasi, E. (2005) · Medical Microbiology and Immunology · doi:10.1007/s00430-005-0243-8 · Cited by 15

Physiology and Pathophysiology of Microglial Cell Function

Streit, W. J. (2002) · Springer eBooks · doi:10.1007/978-1-4757-4139-1_1 · Cited by 14

Alismol, a Sesquiterpenoid Isolated from Vladimiria souliei, Suppresses Proinflammatory Mediators in Lipopolysaccharide-Stimulated Microglia

Shi, D., Song, X., Guo, Y., Xu, J., Liu, Y., Zhang, J., Cui, C., & Jin, D. (2017) · Journal of Molecular Neuroscience · doi:10.1007/s12031-017-0890-4 · Cited by 14

Nitrosporeusine analogue ameliorates Chandipura virus induced inflammatory response in CNS via NFκb inactivation in microglia

Verma, A. K., Waghmare, T. S., Jachak, G. R., Philkhana, S. C., Reddy, D. S., & Basu, A. (2018) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0006648 · Cited by 14

Macelignan inhibits the inflammatory response of microglia and regulates neuronal survival

Zong, K., Liu, X. Z., Sun, Z., Piao, L., Xuan, Y., Jin, Y., & Cui, C. (2019) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2019.577123 · Cited by 13

Latroeggtoxin-VI protects nerve cells and prevents depression by inhibiting NF-κB signaling pathway activation and excessive inflammation

Wang, H., Zhai, Y., Lei, Z., Chen, S., Sun, M., Yin, P., Duan, Z., & Wang, X. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1171351 · Cited by 14

Inhibition of microglial neurotoxicity by ethanol extract of Artemisia asiatica Nakai

Lim, B. O., Chung, H. G., Lee, W., Lee, H., & Suk, K. (2007) · Phytotherapy Research · doi:10.1002/ptr.2304 · Cited by 14

RING finger protein 11 (RNF11) modulates susceptibility to 6-OHDA-induced nigral degeneration and behavioral deficits through NF-κB signaling in dopaminergic cells

Pranski, E. L., Dalal, N. V., Sanford, C. V., Herskowitz, J. H., Gearing, M., Lazo, C. R., Miller, G. W., Lah, J. J., Levey, A. I., & Betarbet, R. S. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.12.018 · Cited by 14

Possible role of propofol's cyclooxygenase-inhibiting property in alleviating dopaminergic neuronal loss in the substantia nigra in an MPTP-induced murine model of Parkinson's disease

Kubo, K., Inada, T., & Shingu, K. (2011) · Brain Research · doi:10.1016/j.brainres.2011.02.079 · Cited by 14

Celastrol Suppresses Morphological and Transcriptional Responses in Microglial Cells Upon Stimulation with Double-Stranded RNA

Nakamichi, K., Kitani, H., Takayama‐Ito, M., Morimoto, K., Kurane, I., & Saijo, M. (2010) · International Journal of Neuroscience · doi:10.3109/00207451003615763 · Cited by 14

Inhibition of inflammatory cytokine secretion from mouse microglia cells by DHMEQ, an NF-κB inhibitor

Takatsuna, H., Morita, S., Nagatsu, T., Sawada, M., & Umezawa, K. (2005) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2005.01.011 · Cited by 14

Genetic Regulation of Nerve Avulsion‐Induced Spinal Cord Inflammation

Olsson, T. P., Lundberg, C., Lidman, O., & Piehl, F. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb05383.x · Cited by 14

Isolation and HIV-1 Infection of Primary Human Microglia From Fetal and Adult Tissue

Borgmann, K., Gendelman, H. E., & Ghorpade, A. (2005) · Humana Press eBooks · doi:10.1385/1-59259-907-9:049 · Cited by 14

Neuroprotective Effects of Rutin and Quercetin Flavonoids in Glaucium corniculatum Methanol and Water Extracts

Koçancı, F. G., & Aslım, B. (2017) · International Journal of Secondary Metabolite · doi:10.21448/ijsm.363347 · Cited by 15

The Suppressive Effect of β-Glucan on the Production of Tumor Necrosis Factor-Alpha in BV2 Microglial Cells

Jung, K. H., Kim, M., Ha, E., Kim, H. K., Kim, Y. O., Kang, S. A., Chung, J., & Yim, S. (2007) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.60608 · Cited by 13

Activation of GIPR Exerts Analgesic and Anxiolytic-Like Effects in the Anterior Cingulate Cortex of Mice

Wang, X., Jiang, Y., Lu, L., Feng, B., Ma, X., Zhang, K., Guan, S., Yang, L., Fan, Q., Zhu, X.-C., et al. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.887238 · Cited by 15

Two New Phomaligols from the Marine-Derived Fungus Aspergillus flocculosus and Their Anti-Neuroinflammatory Activity in BV-2 Microglial Cells

Choi, B.-K., Cho, D.-Y., Choi, D., Trinh, P. T. H., & Shin, H. J. (2021) · Marine Drugs · doi:10.3390/md19020065 · Cited by 13

Neuroinflammation and oxidative injury in developmental neurotoxicity

Milatović, D., Zaja‐Milatovic, S., BREYER, R. M., Aschner, M., & Montine, T. J. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-382032-7.10064-5 · Cited by 13

Microglial responses in the avascular quail retina following transection of the optic nerve

Jeon, G. S., Kang, T., Park, S. W., Kim, D. W., Seo, J. H., & Cho, S. S. (2004) · Brain Research · doi:10.1016/j.brainres.2004.01.093 · Cited by 13

Effects of different parts of Angelica gigas Nakai on brain damages and neuronal death in transient middle artery occlusion/reperfusion-induced ischemic rats

Shin, Y.-J., & Park, Y. (2014) · The Korea Journal of Herbology · doi:10.6116/kjh.2014.29.6.85 · Cited by 13

Dectin-1-CD37 association regulates IL-6 expression during Toxoplasma gondii infection

Yan, J., Wu, B., Huang, B., Huang, S., Jiang, S., & Lü, F. (2014) · Parasitology Research · doi:10.1007/s00436-014-3946-1 · Cited by 14

Nitric oxide inhibits the proliferation of murine microglial MG5 cells by a mechanism involving p21 but independent of p53 and cyclic guanosine monophosphate

Kawahara, K., Gotoh, T., Oyadomari, S., Kuniyasu, A., Kohsaka, S., Mori, M., & Nakayama, H. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)02079-1 · Cited by 13

Infection of stationary human brain aggregates with HIV‐1 SF162 and IIIB results in transient neuronal damage and neurotoxicity

Trillo‐Pazos, G., Kandanearatchi, A., Eyeson, J., King, D. F. L., Vyakarnam, A., & Everall, I. (2004) · Neuropathology and Applied Neurobiology · doi:10.1046/j.0305-1846.2003.00519.x · Cited by 13

FimH adhesin of Escherichia coli K1 type 1 fimbriae activates BV-2 microglia

Lee, J., Shin, S., Teng, C., Hong, S. J., & Kim, K. S. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.06.180 · Cited by 13

Inhibitory Effect of Protaetia brevitarsis seulensis Ethanol Extract on Neuroinflammation in LPS-stimulated BV-2 Microglia

Lee, H. J., Seo, M., Lee, J. H., Kim, I.-W., Kim, S., Hwang, J., & Kim, M.-A. (2019) · JoLS Journal of Life Sciences · doi:10.5352/jls.2019.29.10.1096 · Cited by 13

Exploring the Role of Guanylate-Binding Protein-2 in Activated Microglia-Mediated Neuroinflammation and Neuronal Damage

You, J.-E., Kim, E., Kim, H. W., Kim, J.-S., Kim, K., & Kim, P. (2024) · Biomedicines · doi:10.3390/biomedicines12051130 · Cited by 12

Microglia as potential key regulators in viral-induced neuroinflammation

Ismail, F. S., Faustmann, T. J., Faustmann, P. M., & Corvace, F. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1426079 · Cited by 13

Electrophysiological correlates of inter- and intrahemispheric saccade-related updating of visual space

Peterburs, J., Gajda, K., Hoffmann, K.-P., Daum, I., & Bellebaum, C. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.08.025 · Cited by 12

Cysteine Peptidase Cathepsin X as a Therapeutic Target for Simultaneous TLR3/4-mediated Microglia Activation

Pišlar, A. H., Nedeljković, B. B., Perić, M., Jakoš, T., Zidar, N., & Kos, J. (2022) · Molecular Neurobiology · doi:10.1007/s12035-021-02694-2 · Cited by 16

Synapse preservation and decreased glial reactions following ventral root crush (VRC) and treatment with 4‐hydroxy‐tempo (TEMPOL)

Spejo, A. B., Brandão‐Teles, C., Zuccoli, G. S., & de Oliveira, A. L. R. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24365 · Cited by 12

Thymulin related peptide attenuates inflammation in the brain induced by intracerebroventricular endotoxin injection

Safieh‐Garabedian, B., Jabbur, S. J., Dardenne, M., & Saadé, N. E. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.11.004 · Cited by 12

HIV-1 envelope glycoprotein 120 induces cyclooxygenase-2 expression in astrocytoma cells through a nuclear factor-κB-dependent mechanism

Álvarez, S., Serramía, M. J., Fresno, M., & Muñoz‐Fernández, M. Á. (2007) · NeuroMolecular Medicine · doi:10.1007/bf02685891 · Cited by 12

Murine gammaherpesvirus-68 infects microglia and induces high levels of pro-inflammatory cytokine production

Taylor, W. R., Rasley, A., Bost, K. L., & Marriott, I. (2003) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(03)00011-0 · Cited by 12

Using gene delivery to protect HIV-susceptible CNS cells: Inhibiting HIV replication in microglia

Cordelier, P., & Strayer, D. S. (2006) · Virus Research · doi:10.1016/j.virusres.2005.11.016 · Cited by 12

Antibody-Mediated Inhibition of Integrin α5β1 Blocks Neurotoxic Prion Peptide PrP106–126-Induced Activation of BV2 Microglia

Chang, J., Yang, L., Kouadir, M., Peng, Y., Zhang, S., Shi, F., Zhou, X., Yin, X., & Zhao, D. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9821-6 · Cited by 12

Schizandra chinensis Alkaloids Inhibit Lipopolysaccharide-Induced Inflammatory Responses in BV2 Microglial Cells

Choi, M. S., Kwon, K. J., Jeon, S. J., Go, H. S., Kim, K. C., Ryu, J. R., Lee, J., Han, S., Cheong, J. H., Ryu, J. H., et al. (2009) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2009.17.1.47 · Cited by 12

HIV-1-Associated Dementia

Gabuzda, D. H., Wang, J., & Gorry, P. R. (2002) · Elsevier eBooks · doi:10.1016/b978-044451002-0/50027-0 · Cited by 12

Investigation of the Circular Transcriptome in Alzheimer’s Disease Brain

Gao, Y., Xu, S.-M., Cheng, Y., Takenaka, K., Lindner, G., & Janitz, M. (2024) · Journal of Molecular Neuroscience · doi:10.1007/s12031-024-02236-0 · Cited by 12

Phagocytic functions of microglial cells in the central nervous system and their importance in two neurodegenerative diseases: multiple sclerosis and Alzheimer’s disease

Choucair‐Jaafar, N., Laporte, V., Levy, R., Arnold, A., Gies, J., Poindron, P., & Lombard, Y. (2006) · Open Life Sciences · doi:10.2478/s11535-006-0038-y · Cited by 11

Primary mouse brain pericytes isolated from transgenic Alzheimer mice spontaneously differentiate into a CD11b+ microglial-like cell type in vitro

Hutter-Schmid, B., & Humpel, C. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.08.003 · Cited by 11

Human immunodeficiency virus infection inhibits granulocyte-macrophage colony-stimulating factor–induced microglial proliferation

Cosenza-Nashat, M. A., Zhao, M., Marshall, H. D., Si, Q., Morgello, S., & Lee, S. C. (2007) · Journal of NeuroVirology · doi:10.1080/13550280701549417 · Cited by 11

A pro- and an anti-inflammatory cytokine are synthetised in distinct brain macrophage cells during innate activation

Calvo, C., Amigou, E., Desaymard, C., & Glowinski, J. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.08.005 · Cited by 11

NO-induced apoptosis and ER stress in microglia

Kawahara, K., Mori, M., & Nakayama, H. (2004) · Folia Pharmacologica Japonica · doi:10.1254/fpj.124.399 · Cited by 11

Pro‐apoptotic activity of N‐myc in activation‐induced cell death of microglia

Jung, D. Y., Lee, H., & Suk, K. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03186.x · Cited by 12

Adjudin - A Male Contraceptive with Other Biological Activities

Cheng, C. Y., Xia, W., Wong, E., Xie, Q. R., Shao, J., Liu, T., Quan, Y., Zhang, T., Yang, X. F., Geng, K., et al. (2015) · Recent Patents on Endocrine Metabolic & Immune Drug Discovery · doi:10.2174/1872214809666151029113043 · Cited by 11

Activation of microglia cells is dispensable for the induction of rat retroviral spongiform encephalopathy

Hansen, R. (2001) · Journal of NeuroVirology · doi:10.1080/135502801753248088 · Cited by 11

By-Product Extracts from Castanea sativa Counteract Hallmarks of Neuroinflammation in a Microglial Model

Marrazzo, P., Mandrone, M., Chiocchio, I., Zambonin, L., Barbalace, M. C., Zalambani, C., Angeloni, C., Malaguti, M., Prata, C., Poli, F., et al. (2023) · Antioxidants · doi:10.3390/antiox12040808 · Cited by 10

Extracts of Allium fistulosum Attenuates Pro-Inflammatory Action in the Lipopolysaccharide-Stimulated BV2 Microglia Cells

Park, S.-H., Kim, J.-I., Jeong, Y.-K., & Choi, Y. H. (2011) · Journal of Life Science · doi:10.5352/jls.2011.21.6.796 · Cited by 10

Attenuation of β-amyloid-induced neuroinflammation by KHG21834 in vivo

Kim, E., Hahn, H., Kim, T.-U., Choi, S.-Y., & Cho, S. W. (2010) · BMB Reports · doi:10.3858/bmbrep.2010.43.6.413 · Cited by 10

Borrelia burgdorferi basic membrane protein A could induce chemokine production in murine microglia cell line BV2

Zhao, H., Liu, A., Cui, Y., Zhang, L., Li, B., & Bao, F. (2017) · Microbial Pathogenesis · doi:10.1016/j.micpath.2017.08.036 · Cited by 10

Novel cycloneolignans from Vernicia fordii with inhibitory effects on over-activation of BV2 cells in vitro

Zhao, W., Li, N., Chu, Y., Sun, T., Wang, J., Wang, W., Li, J.-Y., Lin, B., Chen, R., & Hou, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-14062-z · Cited by 10

Anti-Neuroinflammatory and Neuroprotective Effect of Intermedin B Isolated from the Curcuma longa L. via NF-κB and ROS Inhibition in BV2 Microglia and HT22 Hippocampal Cells

Lee, H., Liu, Z., Dong, L., Lee, D., Yoon, D., Oh, H., Kim, Y., An, R., & Lee, D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087390 · Cited by 10

(−)-Nyasol, isolated from Anemarrhena asphodeloides suppresses neuroinflammatory response through the inhibition of I-κBα degradation in LPS-stimulated BV-2 microglial cells

Lee, H. J., Li, H., Chang, H. R., Jung, H., Lee, D. Y., & Ryu, J. (2012) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.3109/14756366.2012.697057 · Cited by 10

Differential Expression of Doublecortin and Microglial Markers in the Rat Brain Following Fractionated Irradiation

Bálentová, S., Hajtmanová, E., Adamkov, M., & Lehotský, J. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1495-8 · Cited by 10

Protective role of fentanyl in lipopolysaccharide‑induced neuroinflammation in BV‑2 cells

Wang, J., Ying-jie, J., & Li, J. (2018) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2018.6590 · Cited by 10

Microglia in the CNS

Chabot, S., & Yong, V. W. (2002) · Humana Press eBooks · doi:10.1007/978-1-59259-108-4_14 · Cited by 10

Glial reaction to volkensin-induced selective degeneration of central neurons

Cevolani, D., Bentivoglio, M., & Strocchi, P. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00445-7 · Cited by 10

Cellular tropisms and co‐receptor usage of HIV‐1 isolates from vertically infected children with neurological abnormalities and rapid disease progression

McCarthy, M., He, J., Auger, D., Geffin, R., Woodson, C., Hutto, C., Wood, C. A., & Scott, G. B. (2002) · Journal of Medical Virology · doi:10.1002/jmv.2185 · Cited by 10

H3K27me3 of Rnf19a promotes neuroinflammatory response during Japanese encephalitis virus infection

Zhu, S., Tao, M., Li, Y., Wang, X., Zhao, Z., Liu, Y., Li, Q., Li, Q., Lu, Y., Si, Y., et al. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02852-4 · Cited by 9

Effect of acetyl-L-carnitine on hypersensitivity in acute recurrent caerulein-induced pancreatitis and microglial activation along the brain’s pain circuitry

McIlwrath, S. L., Starr, M. E., High, A. E., Saitō, H., & Westlund, K. N. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i9.794 · Cited by 9

Quercetin Derivatives from Siegesbeckia glabrescens Inhibit the Expression of COX-2 Through the Suppression of NF-κB Activation in Microglia

Lim, H.-J., Li, H., Kim, J.-Y., & Ryu, J. (2011) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2011.19.1.027 · Cited by 9

Dissociation between hippocampal neuronal loss, astroglial and microglial reactivity after pharmacologically induced reverse glutamate transport

de Yebra, L., Malpesa, Y., Ursu, G., Pugliese, M., Liévens, J.-C., Goff, L. K., & Mahy, N. (2006) · Neurochemistry International · doi:10.1016/j.neuint.2006.06.008 · Cited by 9

Inhibitory effect ofAngelicae Tenuissimae Radixon expressions of cyclooxygenase-2 and inducible nitric oxide synthase in mouse BV2 microglial cells

Lee, S.-H., Choi, H.-Y., Kim, H., Lee, H., Sung, Y.-H., Kim, S., Chang, H., Shin, M.-C., Shin, M., & Kim, C. (2009) · Neurological Research · doi:10.1179/016164109x12537002794048 · Cited by 9

Conditioned Medium Derived from Salidroside-Pretreated Mesenchymal Stem Cell Culture Ameliorates Mouse Lipopolysaccharide-Induced Cerebral Neuroinflammation- Histological and Immunohistochemical Study

Maadawi, Z. M. E. (2017) · International Journal of Stem Cells · doi:10.15283/ijsc16055 · Cited by 9

Mitigation Effects of a Novel Herbal Medicine, Hepad, on Neuroinflammation, Neuroapoptosis, and Neuro-Oxidation

Song, D. H., Kim, G.-J., Lee, K. J., Shin, J. S., Kim, D. H., Park, B., & An, J. H. (2018) · Molecules · doi:10.3390/molecules23112920 · Cited by 9

Microglia in diseases of the central nervous system

Nelson, P. T., Soma, L. A., & Lavi, E. (2002) · Annals of Medicine · doi:10.1080/078538902321117698 · Cited by 222

Microglia in health and disease

Kim, S. U., & de Vellis, J. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20562 · Cited by 687

A review of the role of the microglia in viral infections of the central nervous system

Xia, X. (2012) · Journal of Pathogen Biology

The role of microglia in the development of neurodegeneration

Saitgareeva, A. R., Bulygin, K. V., Фанилевич, Г. И., Beylerli, O., & Ахмадеева, Л. Р. (2020) · Neurological Sciences · doi:10.1007/s10072-020-04468-5 · Cited by 67

Microglia and neuroinflammation: a pathological perspective

Streit (2004) · Journal of Neuroinflammation · doi:10.1186/1742-2094-1-14 · Cited by 1,039