Effects of the Chemokine CCL2 on Blood–Brain Barrier Permeability during Ischemia–Reperfusion Injury
Abstract
The chemokine CCL2 is considered as one of the main effectors driving postischemic infiltration of monocytes into the brain parenchyma. New experimental data, however, suggest that CCL2 could also participate in blood–brain barrier (BBB) ‘opening’ during the transmigration of monocytes. The current study examines the role of CCL2 in regulating BBB permeability after ischemia in vitro. To address this issue, an in vitro BBB model (coculture of astrocytes and brain endothelial cells) was subjected to 5 h of oxygen glucose deprivation, followed by reoxgenation ( in vitro ischemia/reperfusion (I/R)) for 0 to 48 h. During reperfusion, there was a biphasic enhancement of barrier permeability, with a 200-fold increase in barrier permeability to FITC-albumin at 6 h and a further period of disruption around 24 h. The latter coincided with increased secretion of CCL2 by both astrocytes and brain endothelial cells and increased levels of the CCL2 receptor, CCR2. Applying antisense oligonucleotide or neutralizing antibody to block CCL2 significantly decreased I/R-induced enhancement of BBB permeability (approximately twofold) and redistribution of tight-junction (TJ) proteins (occludin, zonula occluden-1, 2, claudin-5). Similarly, absence of CCR2 from endothelial cells caused stabilization of TJ complexes and decreased the permeability of brain endothelial barrier during in vitro I/R. These data suggest CCL2/CCR2 has an important role in regulating brain endothelial permeability and might be a potential novel therapeutic target for stroke.
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The CCL2-CCR2 chemotactic axis is implicated in mediating leukocyte infiltration into the CNS under a variety of conditions including HIV encephalitis, ischemia, prion disease, and stress.
“The CCL2-CCR2 chemotactic axis, in particular, is implicated in mediating leukocyte infiltration into the CNS under a variety of conditions including HIV encephalitis (Eugenin et al, 2006), ischemia (Dimitrijevic et al, 2006), prion disease (Gomez-Nicola et al, 2014), and stress (Wohleb et al, 2013).”
From Repeated Social Defeat, Neuroinflammation, and Behavior: Monocytes Carry the Signal (2017) · cites this paper as Dimitrijevic et al, 2006
Up-regulation of MCP-1 in the brain microenvironment during inflammatory response probably disrupts BBB integrity by redistribution of tight junction proteins, such as occludin and claudin-1, 5 and 11, and reorganization of the actin cytoskeleton in brain microvascular ECs.
“the up-regulation of MCP-1 in the brain microenvironment during inflammatory response probably disrupts BBB integrity by redistribution of tight junction proteins, such as occludin and claudin-1, 5 and 11 and reorganization of the actin cytoskeleton in brain microvascular ECs (Stamatovic et al., 2003, 2005, 2006; Dimitrijevic et al., 2006).”
From The impact of microglial activation on blood-brain barrier in brain diseases (2014) · cites this paper as Dimitrijevic et al., 2006
Cites
Rollins, B. J. (1997) · Blood · doi:10.1182/blood.v90.3.909 · Cited by 1,983 · see citing works
The Molecular Biology of Leukocyte Chemoattractant Receptors
Murphy, P. M. (1994) · Annual Review of Immunology · doi:10.1146/annurev.iy.12.040194.003113 · Cited by 1,197 · see citing works
Inflammatory Mediators and Modulation of Blood–Brain Barrier Permeability
Abbott, N. J. (2000) · Cellular and Molecular Neurobiology · doi:10.1023/a:1007074420772 · Cited by 803 · see citing works
Molecular physiology and pathophysiology of tight junctions in the blood–brain barrier
Huber, J. D., Egleton, R. D., & Davis, T. P. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)02004-x · Cited by 790 · see citing works
Inflammatory Mechanisms after Ischemia and Stroke
Danton, G. H., & Dietrich, W. D. (2003) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/62.2.127 · Cited by 556 · see citing works
Fey, E. G., Wan, K. M., & Penman, S. (1984) · The Journal of Cell Biology · doi:10.1083/jcb.98.6.1973 · Cited by 542 · see citing works
Hallenbeck, J. M., Dutka, A. J., Tanishima, T., Kochanek, P. M., Kumaroo, K. K., Thompson, C. B., Obrenovitch, T. P., & Contreras, T. J. (1986) · Stroke · doi:10.1161/01.str.17.2.246 · Cited by 482 · see citing works
Blood-brain barrier biology and methodology
Pardridge, W. M. (1999) · Journal of NeuroVirology · doi:10.3109/13550289909021285 · Cited by 447 · see citing works
Okada, Y., Copeland, B. R., Mori, E., Tung, M. M., Thomas, W. S., & del Zoppo, G. J. (1994) · Stroke · doi:10.1161/01.str.25.1.202 · Cited by 435 · see citing works
Monocyte Chemoattractant Protein-1 Regulation of Blood–Brain Barrier Permeability
Stamatovic, S. M., Shakui, P., Keep, R. F., Moore, B. B., Kunkel, S. L., van Rooijen, N., & Andjelkovic, A. V. (2005) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600055 · Cited by 415 · see citing works
Self-citationMultiple Molecular Penumbras after Focal Cerebral Ischemia
Sharp, F. R., Lu, A., Tang, Y., & Millhorn, D. E. (2000) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200007000-00001 · Cited by 396 · see citing works
Cerebral microvascular changes in permeability and tight junctions induced by hypoxia-reoxygenation
Mark, K. S., & Davis, T. P. (2002) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00645.2001 · Cited by 394 · see citing works
Stamatovic, S. M., Keep, R. F., Kunkel, S. L., & Andjelkovic, A. V. (2003) · Journal of Cell Science · doi:10.1242/jcs.00755 · Cited by 381 · see citing works
Self-citationKirk, J., Plumb, J., Mirakhur, M., & McQuaid, S. (2003) · The Journal of Pathology · doi:10.1002/path.1434 · Cited by 375 · see citing works
Bolton, S. J., Anthony, D. C., & Perry, V. H. (1998) · Neuroscience · doi:10.1016/s0306-4522(98)00058-x · Cited by 370 · see citing works
Kuroiwa, T., Ting, P., Martínez, H. R., & KLATZO, I. (1985) · Acta Neuropathologica · doi:10.1007/bf00688633 · Cited by 359 · see citing works
Gaillard, P. J., Voorwinden, L. H., Nielsen, J. L., Aa, I., Atsumi, R., Engman, H., Ringbom, C., de Boer, A. G., & Breimer, D. D. (2001) · European Journal of Pharmaceutical Sciences · doi:10.1016/s0928-0987(00)00123-8 · Cited by 332 · see citing works
Inflammatory Mediators of Cerebral Endothelium: A Role in Ischemic Brain Inflammation
Stanimirovic, D. B., & Satoh, K. (2000) · Brain Pathology · doi:10.1111/j.1750-3639.2000.tb00248.x · Cited by 311 · see citing works
Kim, J. S., Gautam, S., Chopp, M., Zaloga, C., Jones, M. L., Ward, P., & Welch, K. (1995) · Journal of Neuroimmunology · doi:10.1016/0165-5728(94)00138-e · Cited by 299 · see citing works
Peters, O., Back, T., Lindauer, U., Busch, C., Megow, D., Dreier, J. P., & Dirnagl, U. (1998) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199802000-00011 · Cited by 298 · see citing works
Monocyte Chemoattractant Protein-1 Deficiency is Protective in a Murine Stroke Model
Hughes, P., ALLEGRINI, P. R., Rudin, M., Perry, V. H., Mir, A. K., & Wießner, C. (2002) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200203000-00008 · Cited by 295 · see citing works
Burns, A. R., Walker, D. C., Brown, E. S., Thurmon, L. T., Bowden, R. A., Keese, C. R., Simon, S. I., Entman, M. L., & Smith, C. W. (1997) · The Journal of Immunology · doi:10.4049/jimmunol.159.6.2893 · Cited by 284 · see citing works
IL-8 activates endothelial cell CXCR1 and CXCR2 through Rho and Rac signaling pathways
Schraufstätter, I. U., Chung, J., & Burger, M. (2001) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2001.280.6.l1094 · Cited by 278 · see citing works
Stoll, G., Jander, S., & Schroeter, M. (2003) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0123-7_3 · Cited by 277 · see citing works
Chemokines and chemokine receptors in the CNS: a possible role in neuroinflammation and patterning
Mennicken, F., Maki, R. A., Souza, E. B. D., & Quirion, R. (1999) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(99)01308-5 · Cited by 276 · see citing works
Plumb, J., McQuaid, S., Mirakhur, M., & Kirk, J. (2002) · Brain Pathology · doi:10.1111/j.1750-3639.2002.tb00430.x · Cited by 274 · see citing works
The adhesion molecule ICAM-1 and its regulation in relation with the blood–brain barrier
Dietrich, J. (2002) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00114-5 · Cited by 267 · see citing works
Neuroscience approached through cell culture
Pfeiffer, S. E. (1982) · CRC Press eBooks · Cited by 253 · see citing works
Blamire, A. M., Anthony, D. C., Rajagopalan, B., Sibson, N. R., Perry, V. H., & Styles, P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-21-08153.2000 · Cited by 245 · see citing works
Molecular and cellular permeability control at the blood-brain barrier
Gloor, S. M., Wachtel, M., Bolliger, M. F., Ishihara, H., Landmann, R., & Frei, K. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00102-3 · Cited by 244 · see citing works
Cytokines and adhesion molecules in stroke and related diseases
Kim, J. S. (1996) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(95)00338-3 · Cited by 213 · see citing works
Monocyte chemoattractant protein-1 messenger RNA expression in rat ischemic cortex.
Wang, X.-K., Yue, T., Barone, F., & Feuerstein, G. (1995) · Stroke · doi:10.1161/01.str.26.4.661 · Cited by 203 · see citing works
Monocyte chemoattractant protein-1 expressed in neurons and astrocytes during focal ischemia in mice
Che, X., Ye, W., Panga, L., Wu, D.-C., & Yang, G. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02328-9 · Cited by 201 · see citing works
Novel lymphocyte-specific CC chemokines and their receptors
Yoshie, O., Imai, T., & Nomiyama, H. (1997) · Journal of Leukocyte Biology · doi:10.1002/jlb.62.5.634 · Cited by 199 · see citing works
Analysis of tight junctions during neutrophil transendothelial migration
Burns, A. R., Bowden, R. A., MacDonell, S. D., Walker, D. C., Odebunmi, T., Donnachie, E., Simon, S. I., Entman, M. L., & Smith, C. W. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.1.45 · Cited by 194 · see citing works
Tsukamoto, T., & Nigám, S. K. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.26.16133 · Cited by 191 · see citing works
Bell, M. D., Taub, D. D., & Perry, V. H. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00083-8 · Cited by 178 · see citing works
Matsumoto, T., Ikeda, K., Mukaida, N., Harada, A., Matsumoto, Y., Yamashita, J., & Matsushima, K. (1997) · PubMed · Cited by 154 · see citing works
Combination of Hypoxia/Aglycemia Compromises In Vitro Blood-Brain Barrier Integrity
Abbruscato, T. J., & Davis, T. P. (1999) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)38186-8 · Cited by 143 · see citing works
Levine, J. B., Kong, J., Nadler, M., & Xu, Z. (1999) · Glia · doi:10.1002/(sici)1098-1136(199912)28:3 · Cited by 141 · see citing works
Self-citationPaul, R. (2003) · Brain · doi:10.1093/brain/awg171 · Cited by 134 · see citing works
Losy, J., & Zaremba, J. (2001) · Stroke · doi:10.1161/hs1101.097380 · Cited by 130 · see citing works
Elements of cerebral microvascular ischaemia
Petty, M. A., & Wettstein, J. G. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00062-5 · Cited by 127 · see citing works
Kastrup, A., Engelhorn, T., Beaulieu, C., de Crespigny, A. J., & Moseley, M. E. (1999) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(99)00121-5 · Cited by 96 · see citing works
Nitric oxide protects blood‐brain barrier in vitro from hypoxia/reoxygenation‐mediated injury
Utepbergenov, D., Mertsch, K., Sporbert, A., Tenz, K., Paul, M., Haseloff, R. F., & Blasig, I. E. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00173-2 · Cited by 91 · see citing works
Kondo, T., Kinouchi, H., 川瀬, 誠., & Yoshimoto, T. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(96)12555-6 · Cited by 70 · see citing works
Anin vitro model for endothelial permeability: Assessment of monolayer integrity
Kazakoff, P. W., McGuire, T. R., Hoie, E. B., Cano, M., & Iversen, P. L. (1995) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/bf02634568 · Cited by 49 · see citing works
Yang, G., Mao, Y. Q., Zhou, L.-F., Ye, W., Liu, X.-H., Gong, C., & Betz, A. L. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00205-3 · Cited by 48 · see citing works
Infiltration of inflammatory cells through brain endothelium.
Couraud, P.-O. (1998) · PubMed · Cited by 40 · see citing works
Morphological changes in acute cerebral ischemia after occlusion and reperfusion in the rat.
Nakagawa, Y., Fujimoto, N., Matsumoto, K., & Cervós-Navarro, J. (1990) · PubMed · Cited by 35 · see citing works
Lindauer, U., Dreier, J. P., Angstwurm, K., Rubin, I., Villringer, A., Einhäupl, K. M., & Dirnagl, U. (1996) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199611000-00008 · Cited by 32 · see citing works
Muruganandam, A., Smith, C., Ball, R., Herring, T., & Stanimirovic, D. B. (2000) · Acta neurochirurgica. Supplementum · doi:10.1007/978-3-7091-6346-7_6 · Cited by 19 · see citing works
Schürer, L., Corvin, S., Röhrich, F., Abels, C., & Baethmann, A. J. (1994) · Springer eBooks · doi:10.1007/978-3-7091-9334-1_13 · Cited by 6 · see citing works
Collins (1998) · doi:10.1002/(sici)1097-4652(199807)176:1
Flagged first, then by citations
1 of the 55 references couldn’t be matched to a known paper.
Cited by
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Neuroinflammation: friend and foe for ischemic stroke
Jayaraj, R. L., Azimullah, S., Beiram, R., Jalal, F. Y., & Rosenberg, G. A. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1516-2 · Cited by 1,438 · see citing works
Blood-brain barrier tight junction permeability and ischemic stroke
Sandoval, K. E., & WITT, K. A. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2008.08.005 · Cited by 957 · see citing works
Blood-brain barrier dysfunction and recovery after ischemic stroke
Jiang, X., Andjelkovic, A. V., Zhu, L., Yang, T., Bennett, M. V. L., Chen, J., Keep, R. F., & Shi, Y. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.10.001 · Cited by 946 · see citing works
Self-citationNeuroinflammatory mechanisms of blood-brain barrier damage in ischemic stroke
Yang, C., Hawkins, K. E., Doré, S., & Candelario-Jalil, E. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00136.2018 · Cited by 871 · see citing works
The impact of microglial activation on blood-brain barrier in brain diseases
da Fonseca, A. C. C., Matias, D., Garcia, C., Amaral, R., Geraldo, L. H., Freitas, C., & Lima, F. R. S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00362 · Cited by 572 · see citing works
The complexity of neurobiological processes in acute ischemic stroke
Brouns, R., & Deyn, P. P. D. (2009) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2009.04.001 · Cited by 527 · see citing works
Brain Endothelial Cell-Cell Junctions: How to “Open” the Blood Brain Barrier
Stamatovic, S. M., Keep, R. F., & Andjelkovic, A. V. (2008) · Current Neuropharmacology · doi:10.2174/157015908785777210 · Cited by 516 · see citing works
Self-citationJurcău, A., & Simion, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010014 · Cited by 515 · see citing works
Role of Chemokines in CNS Health and Pathology: A Focus on the CCL2/CCR2 and CXCL8/CXCR2 Networks
Semple, B. D., Kossmann, T., & Morganti-Kossmann, M. C. (2009) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.240 · Cited by 457 · see citing works
Shi, Y., Zhang, L., Pu, H., Mao, L., Hu, X., Jiang, X., Xu, N., Stetler, R. A., Zhang, F., Liu, X., et al. (2016) · Nature Communications · doi:10.1038/ncomms10523 · Cited by 431 · see citing works
Self-citationMechanism of IL-1β-Induced Increase in Intestinal Epithelial Tight Junction Permeability
Al–Sadi, R., Ye, D., Dokładny, K., & Ma, T. Y. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.8.5653 · Cited by 419 · see citing works
Absence of the Chemokine Receptor CCR2 Protects Against Cerebral Ischemia/Reperfusion Injury in Mice
Dimitrijevic, O. B., Stamatovic, S. M., Keep, R. F., & Andjelkovic, A. V. (2007) · Stroke · doi:10.1161/01.str.0000259709.16654.8f · Cited by 368 · see citing works
Self-citationCeulemans, A.-G., Zgavc, T., Kooijman, R., Hachimi-Idrissi, S., Sarre, S., & Michotte, Y. (2010) · Journal of Neuroinflammation · doi:10.1186/1742-2094-7-74 · Cited by 351 · see citing works
Maldonado, J. R. (2008) · Critical Care Clinics · doi:10.1016/j.ccc.2008.06.004 · Cited by 338 · see citing works
Pathogenesis of acute stroke and the role of inflammasomes
Fann, D. Y., Lee, S.-Y., Manzanero, S., Chunduri, P., Sobey, C. G., & Arumugam, T. V. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.09.004 · Cited by 334 · see citing works
Rajeev, V., Fann, D. Y., Dinh, Q. N., Kim, H. A., Silva, T. M. D., Lai, M. K. P., Chen, C., Drummond, G. R., Sobey, C. G., & Arumugam, T. V. (2022) · Theranostics · doi:10.7150/thno.68304 · Cited by 314 · see citing works
Macrophages prevent hemorrhagic infarct transformation in murine stroke models
Gliem, M., Mausberg, A. K., Lee, J., Simiantonakis, I., van Rooijen, N., Hartung, H., & Jander, S. (2012) · Annals of Neurology · doi:10.1002/ana.23529 · Cited by 284 · see citing works
Repeated Social Defeat, Neuroinflammation, and Behavior: Monocytes Carry the Signal
Weber, M. D., Godbout, J. P., & Sheridan, J. F. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.102 · Cited by 283 · see citing works
Neuroinflammation and Cerebrovascular Disease in Old Age: A Translational Medicine Perspective
Napoli, M. D., & Shah, I. M. (2011) · Journal of Aging Research · doi:10.4061/2011/857484 · Cited by 262 · see citing works
The blood-brain barrier, chemokines and multiple sclerosis
Holman, D. W., Klein, R. S., & Ransohoff, R. M. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.07.019 · Cited by 247 · see citing works
Rangasamy, S., McGuire, P. G., Nitta, C. F., Monickaraj, F., Oruganti, S. R., & Das, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108508 · Cited by 245 · see citing works
Greenwood, J., Heasman, S. J., Alvarez, J. I., Prat, A., Lyck, R., & Engelhardt, B. (2011) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2010.01140.x · Cited by 240 · see citing works
Current status of chemokines in the adult CNS
Goazigo, A. R.-L., Steenwinckel, J. V., Rostène, W. H., & Parsadaniantz, S. M. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.02.001 · Cited by 237 · see citing works
The Role of Selected Pro-Inflammatory Cytokines in Pathogenesis of Ischemic Stroke
Pawluk, H., Woźniak, A., Grześk, G., Kołodziejska, R., Kozakiewicz, M., Kopkowska, E., Grzechowiak, E., & Kozera, G. (2020) · Clinical Interventions in Aging · doi:10.2147/cia.s233909 · Cited by 218 · see citing works
Borlongan, C. V., Kaneko, Y., Maki, M., Yu, S., Ali, M. S., Allickson, J. G., Sanberg, C. D., Kuzmin‐Nichols, N., & Sanberg, P. R. (2009) · Stem Cells and Development · doi:10.1089/scd.2009.0340 · Cited by 206 · see citing works
Chemokines Are Associated With Delirium After Cardiac Surgery
Rudolph, J. L., Ramlawi, B., Kuchel, G. A., McElhaney, J. E., Xie, D., Sellke, F. W., Khabbaz, K. R., Levkoff, S. E., & Marcantonio, E. R. (2008) · The Journals of Gerontology Series A · doi:10.1093/gerona/63.2.184 · Cited by 184 · see citing works
Keep, R. F., Andjelkovic, A. V., Xiang, J., Stamatovic, S. M., Antonetti, D. A., Hua, Y., & Xi, G. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18774666 · Cited by 183 · see citing works
Self-citationMonocyte chemoattractant protein-1 and the blood–brain barrier
Yao, Y., & Tsirka, S. E. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1459-1 · Cited by 175 · see citing works
Regulatory T cells ameliorate tissue plasminogen activator-induced brain haemorrhage after stroke
Mao, L., Li, P., Zhu, W., Cai, W., Liu, Z., Wang, Y., Luo, W., Stetler, R. A., Leak, R. K., Yu, W., et al. (2017) · Brain · doi:10.1093/brain/awx111 · Cited by 177 · see citing works
Role of CCR2 in Inflammatory Conditions of the Central Nervous System
Chu, H. X., Arumugam, T. V., Gelderblom, M., Magnus, T. U., Drummond, G. R., & Sobey, C. G. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.120 · Cited by 170 · see citing works
The role of inflammasomes in vascular cognitive impairment
Poh, L., Sim, W. L., Jo, D., Dinh, Q. N., Drummond, G. R., Sobey, C. G., Chen, C., Lai, M. K. P., Fann, D. Y., & Arumugam, T. V. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00506-8 · Cited by 167 · see citing works
Hu, B., & Arya, A. K. (2018) · Brain Circulation · doi:10.4103/bc.bc_32_18 · Cited by 165 · see citing works
Terao, S., Yılmaz, G., Stokes, K. Y., Russell, J., Ishikawa, M., Kawase, T., & Granger, D. N. (2008) · Stroke · doi:10.1161/strokeaha.107.513150 · Cited by 163 · see citing works
Williams, D. W., Veenstra, M., Gaskill, P. J., Morgello, S., Calderon, T. M., & Berman, J. W. (2014) · Current HIV Research · doi:10.2174/1570162x12666140526114526 · Cited by 161 · see citing works
Ronaldson, P. T., & Davis, T. P. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212802002625 · Cited by 157 · see citing works
Blood-brain barrier function in intracerebral hemorrhage
Keep, R. F., Xiang, J., Ennis, S. R., Andjelkovic, A., Hua, Y., Xi, G., & Hoff, J. T. (2009) · Acta Neurochirurgica Supplementum · doi:10.1007/978-3-211-09469-3_15 · Cited by 185 · see citing works
Self-citationEnciu, A., Gherghiceanu, M., & Popescu, B. O. (2013) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2013/297512 · Cited by 150 · see citing works
Wang, W., Li, M., Chen, Q., & Wang, J. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8952-x · Cited by 149 · see citing works
Chen, S., Shao, L., & Ma, L. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.716825 · Cited by 150 · see citing works
Chu, H. X., Broughton, B. R. S., Kim, H. A., Lee, S., Drummond, G. R., & Sobey, C. G. (2015) · Stroke · doi:10.1161/strokeaha.115.009426 · Cited by 145 · see citing works
Claudin-1-Dependent Destabilization of the Blood–Brain Barrier in Chronic Stroke
Sladojević, N., Stamatovic, S. M., Johnson, A., Choi, J. H. K., Hu, A., Dithmer, S., Blasig, I. E., Keep, R. F., & Andjelkovic, A. V. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1432-18.2018 · Cited by 142 · see citing works
Self-citationThe Role of Chemokines in the Pathophysiology of Major Depressive Disorder
Milenkovic, V. M., Stanton, E. H., Nothdurfter, C., Rupprecht, R., & Wetzel, C. H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092283 · Cited by 142 · see citing works
NLRP3 inflammasome in ischemic stroke: As possible therapeutic target
Alishahi, M., Farzaneh, M., Ghaedrahmati, F., Nejabatdoust, A., Sarkaki, A., & Khoshnam, S. E. (2019) · International Journal of Stroke · doi:10.1177/1747493019841242 · Cited by 142 · see citing works
Leaky brain in neurological and psychiatric disorders: Drivers and consequences
Morris, G., Fernandes, B. S., Puri, B. K., Walker, A. J., Carvalho, A. F., & Berk, M. (2018) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867418796955 · Cited by 144 · see citing works
Occludin Protein Family: Oxidative Stress and Reducing Conditions
Blasig, I. E., Bellmann, C., Cording, J., Vecchio, G. D., Zwanziger, D., Huber, O., & Haseloff, R. F. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3542 · Cited by 139 · see citing works
Reactive astrocytic S1P3 signaling modulates the blood–tumor barrier in brain metastases
Gril, B., Paranjape, A. N., Woditschka, S., Hua, E., Dolan, E. L., Hanson, J., Wu, X., Kloc, W., Iżycka‐Świeszewska, E., Duchnowska, R., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05030-w · Cited by 128 · see citing works
Bernstein, D. L., Zuluaga-Ramirez, V., Gajghate, S., Reichenbach, N. L., Polyak, B., Persidsky, Y., & Rom, S. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x19882264 · Cited by 120 · see citing works
CCL2 disrupts the adherens junction: implications for neuroinflammation
Roberts, T. K., Eugenin, E. A., Lopez, L., Romero, I. A., Weksler, B. B., Couraud, P.-O., & Berman, J. W. (2012) · Laboratory Investigation · doi:10.1038/labinvest.2012.80 · Cited by 115 · see citing works
Liu, X., Zhang, Z. G., Zhang, R. L., Gregg, S. R., Wang, L., Toh, Y., & Chopp, M. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21359 · Cited by 111 · see citing works
Niego, B., & Medcalf, R. L. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.99 · Cited by 102 · see citing works
Induction of Blood Brain Barrier Tight Junction Protein Alterations by CD8 T Cells
Suidan, G. L., Mcdole, J. R., Chen, Y., Pirko, I., & Johnson, A. J. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003037 · Cited by 105 · see citing works
Deleterious Effects of Dihydrotestosterone on Cerebral Ischemic Injury
Cheng, J., Alkayed, N. J., & Hurn, P. D. (2007) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600457 · Cited by 104 · see citing works
Cranial Irradiation Alters the Brain’s Microenvironment and Permits CCR2+ Macrophage Infiltration
Morganti, J. M., Jopson, T. D., Liu, S., Gupta, N. M., & Rosi, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093650 · Cited by 101 · see citing works
Wang, J., Shi, Y., Zhang, L., Zhang, F., Hu, X., Zhang, W., Leak, R. K., Gao, Y., Chen, L., & Chen, J. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.04.014 · Cited by 101 · see citing works
Huang, Y., Wang, J., Cai, J., Qiu, Y., Zheng, H., Lai, X., Sui, X. Y., Wang, Y., Lu, Q., Zhang, Y., et al. (2018) · Theranostics · doi:10.7150/thno.28029 · Cited by 99 · see citing works
Thuc, O. L., Blondeau, N., Nahon, J., & Rovère, C. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12855 · Cited by 98 · see citing works
Monocyte‐related cytokines/chemokines in cerebral ischemic stroke
Bai, M., Sun, R., Cao, B., Feng, J., & Wang, J. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14368 · Cited by 96 · see citing works
Geng, H., Chen, L., Tang, J. Y., Chen, Y., & Wang, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073485 · Cited by 94 · see citing works
McCaffrey, G., Willis, C. L., Staatz, W. D., Nametz, N., Quigley, C. A., Hom, S., Lochhead, J. J., & Davis, T. P. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06113.x · Cited by 93 · see citing works
Review: Delirium in the Elderly: A Comprehensive Review
Mittal, V., Muralee, S., Williamson, D. E., McEnerney, N., Thomas, J. E., Cash, M., & Tampi, R. R. (2011) · American Journal of Alzheimer s Disease & Other Dementias® · doi:10.1177/1533317510397331 · Cited by 92 · see citing works
The CCL2‐CCR2 system affects the progression and clearance of intracerebral hemorrhage
Yao, Y., & Tsirka, S. E. (2012) · Glia · doi:10.1002/glia.22323 · Cited by 90 · see citing works
In vitro modeling of blood–brain barrier and interface functions in neuroimmune communication
Erickson, M. A., Wilson, M., & Banks, W. A. (2020) · Fluids and Barriers of the CNS · doi:10.1186/s12987-020-00187-3 · Cited by 88 · see citing works
Stephan, D., Sbai, O., Wen, J., Couraud, P., Putterman, C., Khrestchatisky, M., & Desplat‐Jégo, S. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-9 · Cited by 87 · see citing works
A review on in vitro model of the blood-brain barrier (BBB) based on hCMEC/D3 cells
Qi, D., Lin, H., Hu, B., & Wei, Y. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.04.020 · Cited by 87 · see citing works
Role of blood cells in ischaemia-reperfusion induced endothelial barrier failure
Rodrigues, S. F., & Granger, D. N. (2010) · Cardiovascular Research · doi:10.1093/cvr/cvq090 · Cited by 87 · see citing works
Androgens’ effects on cerebrovascular function in health and disease
Abi‐Ghanem, C., Robison, L. S., & Zuloaga, K. L. (2020) · Biology of Sex Differences · doi:10.1186/s13293-020-00309-4 · Cited by 88 · see citing works
Possible role of glial cells in the onset and progression of Lyme neuroborreliosis
Ramesh, G., Borda, J. T., Gill, A. F., Ribka, E. P., Morici, L. A., Mottram, P. J., Martin, D. S., Jacobs, M. B., Didier, P. J., & Philipp, M. T. (2009) · Journal of Neuroinflammation · doi:10.1186/1742-2094-6-23 · Cited by 86 · see citing works
Sladojević, N., Stamatovic, S. M., Keep, R. F., Grailer, J. J., Sarma, J. V., Ward, P. A., & Andjelkovic, A. V. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.03.010 · Cited by 85 · see citing works
Self-citationWelch, G. M., Boix, C. A., Schmauch, E., Davila-Velderrain, J., Victor, M. B., Dileep, V., Bozzelli, P. L., Su, Q., Cheng, J. D., Lee, A., et al. (2022) · Science Advances · doi:10.1126/sciadv.abo4662 · Cited by 84 · see citing works
Post-ischemic blood–brain barrier leakage in rats: One-week follow-up by MRI
Durukan, A., Marinković, I., Strbian, D., Pitkonen, M., Pedrono, E., Soinne, L., Abo‐Ramadan, U., & Tatlisumak, T. (2009) · Brain Research · doi:10.1016/j.brainres.2009.05.025 · Cited by 82 · see citing works
McMillin, M., Frampton, G. A., Thompson, M., Galindo, C., Standeford, H. A., Whittington, E., Alpini, G. D., & DeMorrow, S. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-121 · Cited by 82 · see citing works
Chamera, K., Trojan, E., Szuster-Głuszczak, M., & Basta‐Kaim, A. (2019) · Current Neuropharmacology · doi:10.2174/1570159x17666191113101629 · Cited by 80 · see citing works
Inflammatory cytokine release of astrocytes in vitro is reduced by all-trans retinoic acid
van Neerven, S., Nemes, A., Imholz, P., Regen, T., Denecke, B., Johann, S., Beyer, C., Hanisch, U., & Mey, J. (2010) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2010.08.005 · Cited by 78 · see citing works
Guo, X., Liu, R., Jia, M., Wang, Q., & Wu, J. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03923-x · Cited by 79 · see citing works
Truncation of monocyte chemoattractant protein 1 by plasmin promotes blood–brain barrier disruption
Yao, Y., & Tsirka, S. E. (2011) · Journal of Cell Science · doi:10.1242/jcs.082834 · Cited by 76 · see citing works
Zehendner, C. M., Librizzi, L., de Curtis, M., Kuhlmann, C. R. W., & Luhmann, H. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016760 · Cited by 78 · see citing works
Chen, X. F., Threlkeld, S. W., Cummings, E. E., Juan, I., Makeyev, O., Besio, W. G., Gaitanis, J. N., Banks, W. A., Sadowska, G. B., & Stonestreet, B. S. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.043 · Cited by 76 · see citing works
Help-me signaling: Non-cell autonomous mechanisms of neuroprotection and neurorecovery
Xing, C., & Lo, E. H. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.04.004 · Cited by 75 · see citing works
Paul, D., Ge, S., Lemire, Y., Jellison, E. R., Serwanski, D. R., Ruddle, N. H., & Pachter, J. S. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-10 · Cited by 75 · see citing works
Nicotine aggravates the brain postischemic inflammatory response
Bradford, S. T. J., Stamatovic, S. M., Dondeti, R. S., Keep, R. F., & Andjelkovic, A. V. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00928.2010 · Cited by 73 · see citing works
Self-citationJohnson, A., Roach, J. P., Hu, A., Stamatovic, S. M., Żochowski, M., Keep, R. F., & Andjelkovic, A. V. (2018) · The FASEB Journal · doi:10.1096/fj.201700699r · Cited by 69 · see citing works
Self-citationRetractedStrecker, J., Minnerup, J., Schütte‐Nütgen, K., Gess, B., Schäbitz, W., & Schilling, M. (2013) · Stroke · doi:10.1161/strokeaha.111.000528 · Cited by 69 · see citing works
Functions of lipid raft membrane microdomains at the blood–brain barrier
Dodelet-Devillers, A., Cayrol, R., van Horssen, J., Haqqani, A. S., de Vries, H. E., Engelhardt, B., Greenwood, J., & Prat, A. (2009) · Journal of Molecular Medicine · doi:10.1007/s00109-009-0488-6 · Cited by 70 · see citing works
Regenerative Medicine Therapies for Targeting Neuroinflammation After Stroke
Rajkovic, O., Potjewyd, G., & Pinteaux, E. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00734 · Cited by 69 · see citing works
The CCL2-CCR2 astrocyte-cancer cell axis in tumor extravasation at the brain
Hajal, C., Shin, Y., Li, L., Serrano, J. C., Jacks, T., & Kamm, R. D. (2021) · Science Advances · doi:10.1126/sciadv.abg8139 · Cited by 69 · see citing works
Titchenell, P. M., & Antonetti, D. A. (2013) · Diabetes · doi:10.2337/db12-1744 · Cited by 67 · see citing works
17β-Estradiol Ameliorates Tight Junction Disruption via Repression of MMP Transcription
Na, W., Lee, J. Y., Kim, W., Yune, T. Y., & Ju, B. (2015) · Molecular Endocrinology · doi:10.1210/me.2015-1124 · Cited by 65 · see citing works
Chemokines play complex roles in cerebral ischemia
Chen, C., Chu, S., Liu, D., Zhang, Z., Kong, L., Zhou, X., & Chen, N. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.06.008 · Cited by 64 · see citing works
Andjelkovic, A. V., Stamatovic, S. M., Phillips, C. M., Martínez-Revollar, G., & Keep, R. F. (2020) · Fluids and Barriers of the CNS · doi:10.1186/s12987-020-00202-7 · Cited by 63 · see citing works
Self-citationSystemic immune responses after ischemic stroke: From the center to the periphery
Wu, F., Liu, Z., Zhou, L., Ye, D., Zhu, Y., Huang, K., Weng, Y., Xiong, X., Zhan, R., & Shen, J. F. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.911661 · Cited by 62 · see citing works
CCL4 induces inflammatory signalling and barrier disruption in the neurovascular endothelium
Estevao, C., Bowers, C. E., Luo, D., Sarker, M. H., Hoeh, A. E., Frudd, K., Turowski, P., & Greenwood, J. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100370 · Cited by 59 · see citing works
Terao, Y., Ohta, H., Oda, A., Nakagaito, Y., Kiyota, Y., & Shintani, Y. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.01.017 · Cited by 58 · see citing works
Wang, L.-S., Deng, S., Lu, Y., Zhang, Y., Li, Y., Guan, Y., Jiang, H., & Li, H.-Y. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.06.010 · Cited by 56 · see citing works
Zhang, L., Tan, J., Jiang, X., Qian, W., Yang, T., Sun, X., Chen, Z., & Zhu, Q. (2017) · Biological Research · doi:10.1186/s40659-017-0130-y · Cited by 56 · see citing works
Hemorrhagic Transformation After Tissue Plasminogen Activator Treatment in Acute Ischemic Stroke
Liu, C., Xie, J., Sun, S., Li, H., Li, T., Jiang, C. Q., Chen, X., Wang, J., Le, A., Wang, J., et al. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00985-1 · Cited by 58 · see citing works
Stroke-induced damage on the blood–brain barrier
Xue, S., Zhou, X., Yang, Z., Si, X., & Sun, X. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1248970 · Cited by 55 · see citing works
Influence of the extracellular matrix on endogenous and transplanted stem cells after brain damage
Roll, L., & Faissner, A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00219 · Cited by 54 · see citing works
Modulation of Neuroinflammation in the Central Nervous System: Role of Chemokines and Sphingolipids
Gualtierotti, R., Guarnaccia, L., Beretta, M., Navone, S. E., Campanella, R., Riboni, L., Rampini, P. M., & Marfia, G. (2017) · Advances in Therapy · doi:10.1007/s12325-016-0474-7 · Cited by 55 · see citing works
Li, Y., Eskelund, A., Zhou, H., Budac, D. P., Sánchez, C., & Gulinello, M. E. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160715150 · Cited by 54 · see citing works
Ye, Q., Jo, J.-Y., Wang, C., Oh, H., Zhan, J., Choy, T. J., Kim, K. I., D’Alessandro, A., Reshetnyak, Y. K., Jung, S. Y., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114193 · Cited by 53 · see citing works
- Authors
- Dimitrijevic, O. B., Stamatovic, S. M., Keep, R. F., & Andjelkovic, A. V.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Andjelkovic, Anuska V
- Venue
- Journal of Cerebral Blood Flow & Metabolism
- Publisher
- SAGE Publications
- Published
- 2006-06
- Volume
- 26
- Issue
- 6
- Pages
- 797-810
- ISSN
- 0271-678X (ISSN-L)
- 1559-7016
- OpenAlex
- W1995446848
- Cited by
- 252
- References
- 55
- Citations by year
- 2026: 7 · 2025: 11 · 2024: 26 · 2023: 18 · 2022: 19 · 2021: 10 · 2020: 12 · 2019: 9 · 2018: 16 · 2017: 13 · 2016: 11 · 2015: 9 · 2014: 16 · 2013: 16 · 2012: 11
- FWCI
- 2.62
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cerebral Blood Flow & Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Michigan
- National Institute of Neurological Disorders and Stroke (R01NS044907, NS-044907)
- Division of Chemistry
- Topics
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
- Health Sciences › Medicine › Epidemiology › Acute Ischemic Stroke Management
- Keywords
- MCP-1, CCR2, blood-brain barrier permeability, ischemia-reperfusion injury, monocyte transmigration, tight junction proteins, occludin, claudin-5, zonula occludens-1, brain endothelial cells, astrocytes, oxygen-glucose deprivation, stroke, chemokines
- MeSH terms
- Animals, Astrocytes, Blood-Brain Barrier, Capillary Permeability, Cell Movement, Cells, Cultured, Enzyme-Linked Immunosorbent Assay, Fluorescent Antibody Technique, Blotting, Western, Reperfusion Injury, Electric Impedance, Coculture Techniques, Chemokine CCL2, Receptors, Chemokine, Reverse Transcriptase Polymerase Chain Reaction, Endothelial Cells, Mice, Receptors, CCR2
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