The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Protective Role of Reactive Astrocytes in Brain Ischemia
Abstract
Reactive astrocytes are thought to protect the penumbra during brain ischemia, but direct evidence has been lacking due to the absence of suitable experimental models. Previously, we generated mice deficient in two intermediate filament (IF) proteins, glial fibrillary acidic protein (GFAP) and vimentin, whose upregulation is the hallmark of reactive astrocytes. GFAP(-/-)Vim(-/-) mice exhibit attenuated posttraumatic reactive gliosis, improved integration of neural grafts, and posttraumatic regeneration. Seven days after middle cerebral artery (MCA) transection, infarct volume was 210 to 350% higher in GFAP(-/-)Vim(-/-) than in wild-type (WT) mice; GFAP(-/-), Vim(-/-) and WT mice had the same infarct volume. Endothelin B receptor (ET(B)R) immunoreactivity was strong on cultured astrocytes and reactive astrocytes around infarct in WT mice but undetectable in GFAP(-/-)Vim(-/-) astrocytes. In WT astrocytes, ET(B)R colocalized extensively with bundles of IFs. GFAP(-/-)Vim(-/-) astrocytes showed attenuated endothelin-3-induced blockage of gap junctions. Total and glutamate transporter-1 (GLT-1)-mediated glutamate transport was lower in GFAP(-/-)Vim(-/-) than in WT mice. DNA array analysis and quantitative real-time PCR showed downregulation of plasminogen activator inhibitor-1 (PAI-1), an inhibitor of tissue plasminogen activator. Thus, reactive astrocytes have a protective role in brain ischemia, and the absence of astrocyte IFs is linked to changes in glutamate transport, ET(B)R-…
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“Attenuated reactive gliosis in Gfap−/− Vim−/− mice was connected with larger infarctions in a mouse model of focal brain ischemia (32) and facilitated disease progression in a mouse model of Batten's disease (33).”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [32]
In the citing paper
“Further, the effects of acute central nervous system injury are comparable in Gfap−/−, Vim−/−, and wild-type mice (22, 32).”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [32]
In the citing paper
“The intermediate filament proteins GFAP and Vim are expressed at high levels in activated astrocytes and are critical for the activated phenotype.”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [32]
In the citing paper
“Under baseline conditions, however, Gfap−/−Vim−/− mice have astrocytes of normal appearance and grossly normal brain anatomy (22, 23, 32).”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [32]
In the citing paper
“But when Gfap and Vim are both deleted, astrocytes cannot form intermediate filament networks or display reactive morphology (22, 23, 32).”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [32]
Citations
Cites
Identification of a Neural Stem Cell in the Adult Mammalian Central Nervous System
Johansson, C. B., Momma, S., Clarke, D. L., Risling, M., Lendahl, U., & Frisén, J. (1999) · Cell · doi:10.1016/s0092-8674(00)80956-3 · Cited by 1,875
Reactive astrocytes: cellular and molecular cues to biological function
Ridet, J., Privat, A., Malhotra, S. K., & Gage, F. H. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01139-9 · Cited by 1,766
Localization of neuronal and glial glutamate transporters
Rothstein, J. D., Martin, L. J., Levey, A. I., Dykes‐Hoberg, M., Jin, L., Wu, D. M., Nash, N. R., & Kuncl, R. W. (1994) · Neuron · doi:10.1016/0896-6273(94)90038-8 · Cited by 1,703
Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury
Faulkner, J. R., Herrmann, J. E., Woo, M. J., Tansey, K. E., Doan, N., & Sofroniew, M. V. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3547-03.2004 · Cited by 1,652
Molecular profile of reactive astrocytes—Implications for their role in neurologic disease
Eddleston, M., & Mucke, L. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90380-x · Cited by 1,441
Bush, T. G., Puvanachandra, N., Horner, C. H., Polito, A., Ostenfeld, T., Svendsen, C. N., Mucke, L., Johnson, M. H., & Sofroniew, M. V. (1999) · Neuron · doi:10.1016/s0896-6273(00)80781-3 · Cited by 1,116
Okada, S., Nakamura, M., Katoh, H., Miyao, T., Shimazaki, T., Ishii, K., Yamane, J., Yoshimura, A., Iwamoto, Y., Toyama, Y., et al. (2006) · Nature Medicine · doi:10.1038/nm1425 · Cited by 991
Excitotoxin-induced neuronal degeneration and seizure are mediated by tissue plasminogen activator
Tsirka, S. E., Gualandris, A., Amaral, D. G., & Strickland, S. (1995) · Nature · doi:10.1038/377340a0 · Cited by 658
Liedtke, W., Edelmann, W., Bieri, P. L., Chiu, F.-C., Cowan, N. J., Kucherlapati, R., & Raine, C. S. (1996) · Neuron · doi:10.1016/s0896-6273(00)80194-4 · Cited by 538
Gap-junction-mediated propagation and amplification of cell injury
Lin, J. H.-C., Weigel, H., Cotrina, M. L., Liu, S., Bueno, E., Hansen, A. J., Hansen, T. W., Goldman, S. A., & Nedergaard, M. (1998) · Nature Neuroscience · doi:10.1038/2210 · Cited by 481
Flagged first, then by citations
Research works printed but not linked: 1
- Kraig R, 1995, Neuroglia, 964
Cited by
Sorted by citations
Astrocytes: Biology and pathology
Sofroniew, M. V., & Vinters, H. V. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0619-8 · Cited by 5,196
Molecular dissection of reactive astrogliosis and glial scar formation
Sofroniew, M. V. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.08.002 · Cited by 2,594
Reactive Gliosis and the Multicellular Response to CNS Damage and Disease
Burda, J. E., & Sofroniew, M. V. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.034 · Cited by 1,500
Astrocyte barriers to neurotoxic inflammation
Sofroniew, M. V. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3898 · Cited by 1,202
STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury
Herrmann, J. E., Imura, T., Song, B., Qi, J., Ao, Y., Nguyen, T. K., Korsak, R. A., Takeda, K., Akira, S., & Sofroniew, M. V. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1709-08.2008 · Cited by 958
Astrocyte reactivity and reactive astrogliosis: costs and benefits
Pekny, M., & Pekna, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00041.2013 · Cited by 934
Self-citationHol, E. M., & Pekny, M. (2015) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2015.02.004 · Cited by 917
Self-citationIntegrated Brain Circuits: Astrocytic Networks Modulate Neuronal Activity and Behavior
Halassa, M. M., & Haydon, P. G. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135843 · Cited by 763
Astrocytes: a central element in neurological diseases
Pekny, M., Pekna, M., Messing, A., Steinhäuser, C., Lee, J., Parpura, V., Hol, E. M., Sofroniew, M. V., & Verkhratsky, A. (2015) · Acta Neuropathologica · doi:10.1007/s00401-015-1513-1 · Cited by 793
Self-citationSofroniew, M. V. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020420 · Cited by 695
The dual role of astrocyte activation and reactive gliosis
Pekny, M., Wilhelmsson, U., & Pekna, M. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2013.12.071 · Cited by 693
Self-citationGlial Cells: Role of the Immune Response in Ischemic Stroke
Xu, S., Lü, J., Shao, A., Zhang, J. H., & Zhang, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00294 · Cited by 626
Astrocytes, therapeutic targets for neuroprotection and neurorestoration in ischemic stroke
Liu, Z., & Chopp, M. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.09.008 · Cited by 610
Stroke and the immune system: from pathophysiology to new therapeutic strategies
Macrez, R., Ali, C., Toutirais, O., Mauff, B. L., Defer, G. L., Dirnagl, U., & Vivien, D. (2011) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70066-7 · Cited by 559
The stem cell potential of glia: lessons from reactive gliosis
Robel, S., Berninger, B., & Götz, M. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn2978 · Cited by 536
Nanomaterials for Neural Interfaces
Kotov, N. A., Winter, J. O., Clements, I. P., Jan, E., Timko, B. P., Campidelli, S., Pathak, S., Mazzatenta, A., Lieber, C. M., Prato, M., et al. (2009) · Advanced Materials · doi:10.1002/adma.200801984 · Cited by 504
Voskuhl, R. R., Peterson, R. S., Song, B., Ao, Y., Morales, L. B. J., Tiwari-Woodruff, S. K., & Sofroniew, M. V. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1514-09.2009 · Cited by 478
Astrocytes in Alzheimer's Disease
Verkhratsky, A., Olabarria, M., Noristani, H. N., Yeh, C., & Rodriguez, J. J. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2010.05.017 · Cited by 470
Regulation of Blood Pressure and Salt Homeostasis by Endothelin
Kohan, D. E., Rossi, N. F., Inscho, E. W., & Pollock, D. M. (2011) · Physiological Reviews · doi:10.1152/physrev.00060.2009 · Cited by 430
Reactive Astrocytes As Therapeutic Targets for CNS Disorders
Hamby, M. E., & Sofroniew, M. V. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2010.07.003 · Cited by 381
Multiple Roles for Astrocytes as Effectors of Cytokines and Inflammatory Mediators
Sofroniew, M. V. (2014) · The Neuroscientist · doi:10.1177/1073858413504466 · Cited by 333
Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice
Kraft, A. W., Hu, X., Yoon, H., Yan, P., Xiao, Q., Wang, Y., Gil, S. C., Brown, J., Wilhelmsson, U., Restivo, J. L., et al. (2013) · The FASEB Journal · doi:10.1096/fj.12-208660 · Cited by 324
Self-citationBuffo, A., Rolando, C., & Ceruti, S. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.09.014 · Cited by 338
Astrogliosis: An integral player in the pathogenesis of Alzheimer's disease
Osborn, L. M., Kamphuis, W., Wadman, W. J., & Hol, E. M. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.01.001 · Cited by 312
Neuroglia in neurodegeneration
Heneka, M. T., Rodriguez, J. J., & Verkhratsky, A. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.11.004 · Cited by 316
Astrocytes: Targets for Neuroprotection in Stroke
Barreto, G. E., White, R., Ouyang, Y., Xu, L., & Giffard, R. G. (2011) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/187152411796011303 · Cited by 286
Reactive gliosis in the pathogenesis of CNS diseases
Pekny, M., & Pekna, M. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.11.014 · Cited by 289
Self-citationGlial Cells as Progenitors and Stem Cells: New Roles in the Healthy and Diseased Brain
Dimou, L., & Götz, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00036.2013 · Cited by 285
Seizure-Induced Oxidative Stress in Temporal Lobe Epilepsy
Puttachary, S., Sharma, S., Stark, S., & Thippeswamy, T. (2015) · BioMed Research International · doi:10.1155/2015/745613 · Cited by 268
Roles of vimentin in health and diseasePreprint
Ridge, K. M., Eriksson, J., Pekny, M., & Goldman, R. D. (2022) · Genes & Development · doi:10.1101/gad.349358.122 · Cited by 271
Self-citationModulation of Neural Plasticity as a Basis for Stroke Rehabilitation
Pekna, M., Pekny, M., & Nilsson, M. (2012) · Stroke · doi:10.1161/strokeaha.112.654228 · Cited by 274
Self-citationReactive astrocytes and therapeutic potential in focal ischemic stroke
Choudhury, G. R., & Ding, S. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.05.003 · Cited by 262
van Velthoven, C. T. J., Kavelaars, A., van Bel, F., & Heijnen, C. J. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2009.10.017 · Cited by 251
Cerbai, F., Lana, D., Nosi, D., Petkova-Kirova, P., Zecchi, S., Brothers, H. M., Wenk, G. L., & Giovannini, M. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045250 · Cited by 251
Neurological Diseases as Primary Gliopathies: A Reassessment of Neurocentrism
Verkhratsky, A., Sofroniew, M. V., Messing, A., deLanerolle, N. C., Rempe, D. A., Rodriguez, J. J., & Nedergaard, M. (2012) · ASN NEURO · doi:10.1042/an20120010 · Cited by 254
Kamphuis, W., Middeldorp, J., Kooijman, L., Sluijs, J. A., Kooi, E., Moeton, M., Freriks, M., Mizee, M. R., & Hol, E. M. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.09.035 · Cited by 251
Stratification of astrocytes in healthy and diseased brain
Verkhratsky, A., Zorec, R., & Parpura, V. (2017) · Brain Pathology · doi:10.1111/bpa.12537 · Cited by 236
Astrocyte activation and reactive gliosis—A new target in stroke?
Pekny, M., Wilhelmsson, U., Tatlisumak, T., & Pekna, M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.07.021 · Cited by 240
Self-citationGlial Cells Shape Pathology and Repair After Spinal Cord Injury
Gaudet, A. D., & Fonken, L. K. (2018) · Neurotherapeutics · doi:10.1007/s13311-018-0630-7 · Cited by 242
The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
Becerra-Calixto, A., & Cardona‐Gómez, G. P. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00088 · Cited by 239
Blood-Brain Barrier Dysfunction in CNS Disorders and Putative Therapeutic Targets: An Overview
Archie, S. R., Shoyaib, A. A., & Cucullo, L. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13111779 · Cited by 244
Astrocytes: Integrative Regulators of Neuroinflammation in Stroke and Other Neurological Diseases
Cekanaviciute, E., & Buckwalter, M. S. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0477-8 · Cited by 229
Brenner, M. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.01.055 · Cited by 222
Protective Functions of Reactive Astrocytes Following Central Nervous System Insult
Linnerbauer, M., & Rothhammer, V. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.573256 · Cited by 235
Rational modulation of the innate immune system for neuroprotection in ischemic stroke
Amantea, D., Micieli, G., Tassorelli, C., Cuartero, M. I., Ballesteros, I., Certo, M., Moro, M. Á., Lizasoaín, I., & Bagetta, G. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00147 · Cited by 224
Cekanaviciute, E., Fathali, N., Doyle, K. P., Williams, A. M., Han, J., & Buckwalter, M. S. (2014) · Glia · doi:10.1002/glia.22675 · Cited by 209
Pathophysiology of astroglial purinergic signalling
Franke, H., Verkhratsky, A., Burnstock, G., & Illés, P. (2012) · Purinergic Signalling · doi:10.1007/s11302-012-9300-0 · Cited by 210
Liu, Z., Li, Y., Cui, Y., Roberts, C. J., Lü, M., Wilhelmsson, U., Pekny, M., & Chopp, M. (2014) · Glia · doi:10.1002/glia.22723 · Cited by 205
Self-citationAmankulor, N. M., Hambardzumyan, D., Pyonteck, S. M., Becher, O. J., Joyce, J. A., & Holland, E. C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2500-09.2009 · Cited by 200
Burnstock, G., & Verkhratsky, A. (2010) · Cell Death and Disease · doi:10.1038/cddis.2009.11 · Cited by 202
Xiong, X., Barreto, G. E., Xu, L., Ouyang, Y., Xie, X., & Giffard, R. G. (2011) · Stroke · doi:10.1161/strokeaha.110.593772 · Cited by 199
MiRNA-124 induces neuroprotection and functional improvement after focal cerebral ischemia
Hamzei Taj, S., Kho, W., Riou, A., Wiedermann, D., & Hoehn, M. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.03.025 · Cited by 175
Xing, F., Kobayashi, A., Okuda, H., Watabe, M., Pai, S. K., Pandey, P. R., Hirota, S., Wilber, A. C., Mo, Y., Moore, B. E., et al. (2013) · EMBO Molecular Medicine · doi:10.1002/emmm.201201623 · Cited by 192
Verkhratsky, A., & Burnstock, G. (2014) · BioEssays · doi:10.1002/bies.201400024 · Cited by 185
Kim, R. Y., Hoffman, A., Itoh, N., Ao, Y., Spence, R. D., Sofroniew, M. V., & Voskuhl, R. R. (2014) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2014.06.009 · Cited by 178
The sigma-1 receptor enhances brain plasticity and functional recovery after experimental stroke
Ruscher, K., Shamloo, M., Rickhag, M., Ladunga, I., Soriano, L., Gisselsson, L., Toresson, H., Ruslim-Litrus, L., Oksenberg, D., Urfer, R., et al. (2011) · Brain · doi:10.1093/brain/awq367 · Cited by 183
Plasticity in the Neonatal Brain following Hypoxic-Ischaemic Injury
Rocha‐Ferreira, E., & Hristova, M. (2016) · Neural Plasticity · doi:10.1155/2016/4901014 · Cited by 184
Reduced astrocytic NF-κB activation by laquinimod protects from cuprizone-induced demyelination
Brück, W., Pförtner, R., Pham, T., Zhang, J., Hayardeny, L., Piryatinsky, V., Hanisch, U., Regen, T., van Rossum, D., Brakelmann, L., et al. (2012) · Acta Neuropathologica · doi:10.1007/s00401-012-1009-1 · Cited by 168
Neural cell cycle dysregulation and central nervous system diseases
Wang, W., Bu, B., Xie, M., Zhang, M., Yu, Z., & Tao, D. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.01.007 · Cited by 164
Glial calcium and diseases of the nervous system
Nedergaard, M., Rodriguez, J. J., & Verkhratsky, A. (2010) · Cell Calcium · doi:10.1016/j.ceca.2009.11.010 · Cited by 163
Glia in the pathogenesis of neurodegenerative diseases
Verkhratsky, A., Parpura, V., Pekna, M., Pekny, M., & Sofroniew, M. (2014) · Biochemical Society Transactions · doi:10.1042/bst20140107 · Cited by 141
Self-citationNeuroinflammation as a Key Driver of Secondary Neurodegeneration Following Stroke?
Stuckey, S. M., Ong, L. K., Collins‐Praino, L. E., & Turner, R. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222313101 · Cited by 162
Kamphuis, W., Kooijman, L., Orre, M., Stassen, O., Pekny, M., & Hol, E. M. (2015) · Glia · doi:10.1002/glia.22800 · Cited by 155
Self-citationVenkat, P., Chopp, M., & Chen, J. (2017) · Journal of the American Heart Association · doi:10.1161/jaha.117.005819 · Cited by 165
Li, H., Zhang, N., Lin, H., Yu, Y., Cai, Q., Ma, L., & Ding, S. (2014) · BMC Neuroscience · doi:10.1186/1471-2202-15-58 · Cited by 155
Brain-derived estrogen and neural function
Brann, D. W., Lu, Y., Wang, J., Zhang, Q., Thakkar, R., Sareddy, G. R., Pratap, U. P., TEKMAL, R. R., & Vadlamudi, R. K. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.014 · Cited by 164
Ren, Y., Ao, Y., O’Shea, T. M., Burda, J. E., Bernstein, A. M., Brumm, A. J., Muthusamy, N., Ghashghaei, H. T., Carmichael, S. T., Cheng, L., et al. (2017) · Scientific Reports · doi:10.1038/srep41122 · Cited by 152
Functional dissection of astrocyte-secreted proteins: Implications in brain health and diseases
Jha, M. K., Kim, J.-H., Song, G. J., Lee, W., Lee, I. K., Lee, H., An, S. S. A., Kim, S., & Suk, K. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.12.003 · Cited by 156
“Targeting astrocytes in CNS injury and disease: A translational research approach”
Filous, A. R., & Silver, J. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.03.009 · Cited by 151
Glial Fibrillary Acidic Protein (GFAP): Neuroinflammation Biomarker in Acute Ischemic Stroke
Amalia, L. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s342097 · Cited by 145
Morris, G., & Maes, M. H. J. (2014) · Current Neuropharmacology · doi:10.2174/1570159x11666131120224653 · Cited by 143
Optic nerve astrocyte reactivity protects function in experimental glaucoma and other nerve injuries
Sun, D., Moore, S., & Jakobs, T. C. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20160412 · Cited by 130
Reactive astrogliosis in stroke: Contributions of astrocytes to recovery of neurological function
Sims, N. R., & Yew, W. P. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2016.12.016 · Cited by 149
Stephen, T., Higgs, N., Sheehan, D. F., Awabdh, S. A., López‐Doménech, G., Arancibia‐Cárcamo, I. L., & Kittler, J. T. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2068-15.2015 · Cited by 140
Blood biomarkers in ischemic stroke: potential role and challenges in clinical practice and research
Makris, K., Haliassos, A., Chondrogianni, M. E., & Tsivgoulis, G. K. (2018) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408363.2018.1461190 · Cited by 130
Antidepressants act directly on astrocytes: Evidences and functional consequences
Czéh, B., & Benedetto, B. D. (2012) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.04.017 · Cited by 132
Abnormal Reactivity of Müller Cells after Retinal Detachment in Mice Deficient in GFAP and Vimentin
Verardo, M. R., Lewis, G. P., Takeda, M., Linberg, K. A., Byun, J., Luna, G., Wilhelmsson, U., Pekny, M., Chen, D., & Fisher, S. K. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-1474 · Cited by 129
Self-citationDiversity of astroglial responses across human neurodegenerative disorders and brain aging
Ferrer, I. (2017) · Brain Pathology · doi:10.1111/bpa.12538 · Cited by 135
Clark, D. P. Q., Perreau, V. M., Shultz, S. R., Brady, R. D., Lei, E., Dixit, S., Taylor, J. M., Beart, P. M., & Boon, W. C. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02721-8 · Cited by 132
Mizee, M. R., Nijland, P. G., van der Pol, S. M. A., Drexhage, J., Hof, B. V. H., Mebius, R. E., van der Valk, P., van Horssen, J., Reijerkerk, A., & de Vries, H. E. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1335-6 · Cited by 131
Involvement of p38 MAPK in reactive astrogliosis induced by ischemic stroke
Choudhury, G. R., Ryou, M., Poteet, E. C., Wen, Y., He, R., Sun, F., Fang, Y., Jin, K., & Yang, S. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.013 · Cited by 124
Peri-Infarct Upregulation of the Oxytocin Receptor in Vascular Dementia
McKay, E. C., Beck, J. S., Khoo, S. K., Dykema, K. J., Cottingham, S. L., Winn, M. E., Paulson, H. L., Lieberman, A. P., & Counts, S. (2019) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlz023 · Cited by 121
Glial fibrillary acidic protein is a body fluid biomarker for glial pathology in human disease
Petzold, A. (2014) · Brain Research · doi:10.1016/j.brainres.2014.12.027 · Cited by 121
Messing, A., & Brenner, M. (2020) · ASN NEURO · doi:10.1177/1759091420949680 · Cited by 120
Proliferating Reactive Astrocytes Are Regulated by Notch-1 in the Peri-Infarct Area After Stroke
Shimada, I. S., Borders, A., Aronshtam, A., & Spees, J. L. (2011) · Stroke · doi:10.1161/strokeaha.111.623280 · Cited by 118
Vardjan, N., Gabrijel, M., Potokar, M., Švajger, U., Kreft, M., Jeras, M., de Pablo, Y., Faiz, M., Pekny, M., & Zorec, R. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-144 · Cited by 117
Self-citationTargeted Activation of Astrocytes: A Potential Neuroprotective Strategy
Escartin, C., & Bonvento, G. (2008) · Molecular Neurobiology · doi:10.1007/s12035-008-8043-y · Cited by 118
CD36 is Involved in Astrocyte Activation and Astroglial Scar Formation
Bao, Y., Qin, L., Kim, E., Bhosle, S., Guo, H., Febbraio, M., Haskew-Layton, R. E., Ratan, R., & Cho, S. (2012) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2012.52 · Cited by 102
New Aspects of the Pathogenesis of Canine Distemper Leukoencephalitis
Lempp, C., Spitzbarth, I., Puff, C., Cana, A., Kegler, K., Techangamsuwan, S., Baumgärtner, W., & Seehusen, F. (2014) · Viruses · doi:10.3390/v6072571 · Cited by 124
The Relationship of Astrocytes and Microglia with Different Stages of Ischemic Stroke
Liang, Z., Lou, Y., Hao, Y., Li, H., Feng, J., & Liu, S. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230718104634 · Cited by 113
Song, M., Lee, J., Bae, J., Bu, Y., & Kim, E.-C. (2017) · Cell Transplantation · doi:10.3727/096368916x694391 · Cited by 109
Lu, Y., Sareddy, G. R., Wang, J., Zhang, Q., Tang, F., Pratap, U. P., TEKMAL, R. R., Vadlamudi, R. K., & Brann, D. W. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0115-20.2020 · Cited by 111
de Pablo, Y., Nilsson, M., Pekna, M., & Pekny, M. (2013) · Histochemistry and Cell Biology · doi:10.1007/s00418-013-1110-0 · Cited by 111
Self-citationAstrocytic YAP Promotes the Formation of Glia Scars and Neural Regeneration after Spinal Cord Injury
Xie, C., Shen, X., Xu, X., Liu, H., Li, F., Lu, S., Gao, Z., Zhang, J., Wu, Q., Yang, D., et al. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2229-19.2020 · Cited by 114
PDGFR-β as a Positive Regulator of Tissue Repair in a Mouse Model of Focal Cerebral Ischemia
Shen, J. M., Ishii, Y., Xu, G., Dang, T. C., Hamashima, T., Matsushima, T., Yamamoto, S., Hattori, Y., Takatsuru, Y., Nabekura, J., et al. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.136 · Cited by 111
Raasch, J., Zeller, N., van Loo, G., Merkler, D., Mildner, A., Erny, D., Knobeloch, K.-P., Bethea, J. R., Waisman, A., Knust, M., et al. (2011) · Brain · doi:10.1093/brain/awq359 · Cited by 106
Chechneva, O. V., Mayrhofer, F., Daugherty, D. J., Krishnamurty, R. G., Bannerman, P. G. C., Pleasure, D., & Deng, W. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.446 · Cited by 105
Ståhlberg, A., Andersson, D., Aurelius, J., Faiz, M., Pekna, M., Kubista, M., & Pekny, M. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1182 · Cited by 101
Self-citationThe Role of Attenuated Astrocyte Activation in Infantile Neuronal Ceroid Lipofuscinosis
Macauley, S. L., Pekny, M., & Sands, M. S. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3579-11.2011 · Cited by 102
Self-citationXin, H., Li, Y., Shen, L. H., Liu, X., Wang, X., Zhang, J., Pourabdollah-Nejad D, S., Zhang, C., Zhang, L., Jiang, H., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009027 · Cited by 101
Metadata
- Authors
- Li, L., Lundkvist, A., Andersson, D., Wilhelmsson, U., Nagai, N., Pardo, A. C., Nodin, C., Ståhlberg, A., Aprico, K., Larsson, K., Yabe, T., Moons, L., Fotheringham, A., Davies, I., Carmeliet, P., Schwartz, J. P., Pekna, M., Kubista, M., Blomstrand, F., Maragakis, N., Nilsson, M., & Pekny, M.
- Affiliations
- University of Gothenburg (SE)
- KU Leuven (BE)
- Johns Hopkins University (US)
- Tataa Biocenter (Sweden) (SE)
- Center for Brain Repair and Rehabilitation, Department of Clinical Neuroscience and Rehabilitation, Institute of Neuroscience and Physiology at Sahlgrenska Academy, Göteborg University, Göteborg, Sweden
- National Institutes of Health (US)
- University of Manchester (GB)
- Corresponding author
- Pekny, Milos
- ORCID
- Venue
- Journal of Cerebral Blood Flow & Metabolism
- Publisher
- SAGE Publications
- Published
- 2007-08-29
- Volume
- 28
- Issue
- 3
- Pages
- 468-481
- ISSN
- 0271-678X (ISSN-L)
- 1559-7016
- OpenAlex
- W1999495459
- Cited by
- 505
- References
- 43
- Citations by year
- 2026: 6 · 2025: 13 · 2024: 19 · 2023: 23 · 2022: 19 · 2021: 31 · 2020: 24 · 2019: 34 · 2018: 34 · 2017: 30 · 2016: 34 · 2015: 35 · 2014: 46 · 2013: 28 · 2012: 35
- FWCI
- 13.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cerebral Blood Flow & Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Lirias (submittedVersion)
- Chalmers Publication Library (Chalmers University of Technology) (submittedVersion)
- Chalmers Research (Chalmers University of Technology) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Clinical Neurology › Acute Ischemic Stroke Management
- Life Sciences › Neuroscience › Neurology › Neuroprotection in Cerebral Ischemia
- Keywords
- reactive astrocytes, cerebral ischemia, ischemic penumbra, glial fibrillary acidic protein, vimentin, intermediate filaments, endothelin B receptor, endothelin-3, gap junctions, GLT-1, glutamate uptake, plasminogen activator inhibitor-1, infarct size, middle cerebral artery occlusion, reactive gliosis
- MeSH terms
- Animals, Astrocytes, Brain Ischemia, Glial Fibrillary Acidic Protein, Vimentin, Plasminogen Activator Inhibitor 1, Gap Junctions, Mice, Knockout, Glutamic Acid, Middle Cerebral Artery, Receptor, Endothelin B, Mice
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