The DOI matches its Crossref record; 126 of the 126 references it cites were found in a registry or an index.
Absence of Glial Fibrillary Acidic Protein and Vimentin Prevents Hypertrophy of Astrocytic Processes and Improves Post-Traumatic Regeneration
Open accessAbstract
The regenerative capacity of the CNS is extremely limited. The reason for this is unclear, but glial cell involvement has been suspected, and oligodendrocytes have been implicated as inhibitors of neuroregeneration (Chen et al., 2000, GrandPre et al., 2000; Fournier et al., 2001). The role of astrocytes in this process was proposed but remains incompletely understood (Silver and Miller, 2004). Astrocyte activation (reactive gliosis) accompanies neurotrauma, stroke, neurodegenerative diseases, or tumors. Two prominent hallmarks of reactive gliosis are hypertrophy of astrocytic processes and upregulation of intermediate filaments. Using the entorhinal cortex lesion model in mice, we found that reactive astrocytes devoid of the intermediate filament proteins glial fibrillary acidic protein and vimentin (GFAP-/-Vim-/-), and consequently lacking intermediate filaments (Colucci-Guyon et al., 1994; Pekny et al., 1995; Eliasson et al., 1999), showed only a limited hypertrophy of cell processes. Instead, many processes were shorter and not straight, albeit the volume of neuropil reached by a single astrocyte was the same as in wild-type mice. This was accompanied by remarkable synaptic regeneration in the hippocampus. On a molecular level,GFAP-/-Vim-/-reactive astrocytes could not upregulate endothelin B receptors, suggesting that the upregulation is intermediate filament dependent. These findings show a novel role for intermediate filaments in astrocytes and implicate reactive astrocytes as potent inhibitors of neuroregeneration.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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 [23]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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 [23]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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 [23]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“On a cellular level, astrocytes of Gfap−/−Vim−/− mice in the injured area do not develop the characteristic hypertrophy of proximal processes (23).”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [23]
The cited source says what the claim attributes to it.
In the citing paper
“Interestingly, Gfap−/−Vim−/− mice exhibit better posttraumatic regeneration of neuronal synapses (23) and axons (34), increased baseline and posttraumatic neurogenesis (35), and improved functional recovery after spinal cord trauma (36).”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [23]
The cited source says what the claim attributes to it.
In the citing paper
“In several models of acute central nervous system injury, deletion of the genes encoding these proteins suppresses morphological changes associated with astrocyte activation (22, 23, 26, 30, 32, 36).”
From Attenuating astrocyte activation accelerates plaque pathogenesis in APP/PS1 mice (2013) · cites this paper as [23]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A new mathematical model for relative quantification in real-time RT-PCR
Pfaffl, M. W. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.9.e45 · Cited by 34,610
Antibodies, a laboratory manual
(1989) · Biomedicine & Pharmacotherapy · doi:10.1016/0753-3322(89)90130-3 · Cited by 12,318
Bustin, S. A. (2000) · Journal of Molecular Endocrinology · doi:10.1677/jme.0.0250169 · Cited by 3,844
Embedding in Epoxy Resins for Ultrathin Sectioning in Electron Microscopy
Richardson, K. C., Jarett, L., & Finke, E. H. (1960) · Stain Technology · doi:10.3109/10520296009114754 · Cited by 3,310
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
Ischemic Cell Death in Brain Neurons
Lipton, P. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.4.1431 · Cited by 3,043
Thresholds in cerebral ischemia - the ischemic penumbra.
Astrup, J., Siesjö, B. K., & Symon, L. (1981) · Stroke · doi:10.1161/01.str.12.6.723 · Cited by 2,820
The blood–brain barrier: an overview
Ballabh, P., Braun, A., & Nedergaard, M. (2004) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.12.016 · Cited by 2,276
Glutamate-mediated astrocyte–neuron signalling
Parpura, V., Basarsky, T. A., Liu, F., Jeftinija, K., Jeftinija, S., & Haydon, P. G. (1994) · Nature · doi:10.1038/369744a0 · Cited by 1,768
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
Research works printed but not linked: 5
- 1999, J Biol Chem, 274, 3996
- 2000, Invest Ophthalmol Vis Sci, 41, 4268
- 2001, Prog Brain Res, 132, 23
- 1969, Stain Technol, 35, 313
- 1997, Trends Neurosci, 12, 570
Cited by
Sorted by citations
Items 201–300 of 455
Teo, J. D., Morris, M. J., & Jones, N. M. (2015) · Pediatric Research · doi:10.1038/pr.2015.47 · Cited by 41
Clasadonte, J., & Haydon, P. G. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02839.x · Cited by 40
Regulated Exocytosis and Vesicle Trafficking in Astrocytes
Kreft, M., Potokar, M., Stenovec, M., Pangršič, T., & Zorec, R. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2008.04005.x · Cited by 42
Báez-Jurado, E., Guio-Vega, G. P., Aliev, G. M., Tarasov, V. V., Esquinas, P., Echeverrı́a, V., & Barreto, G. E. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0481-y · Cited by 40
Germundson, D. L., Smith, N. A., Vendsel, L. P., Kelsch, A. V., Combs, C. K., & Nagamoto‐Combs, K. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1146-0 · Cited by 40
Kinetics of endothelin‐induced inhibition and glucose permeability of astrocyte gap junctions
Blomstrand, F., & Giaume, C. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20801 · Cited by 40
Viedma-Poyatos, Á., González-Jiménez, P., Pajares, M. A., & Pérez‐Sala, D. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102415 · Cited by 42
Jagged1 regulates the activation of astrocytes via modulation of NFκB and JAK/STAT/SOCS pathways
Morga, E., Mouad‐Amazzal, L., Felten, P., Heurtaux, T., Moro, M., Michelucci, A., Gabel, S., Grandbarbe, L., & Heuschling, P. (2009) · Glia · doi:10.1002/glia.20887 · Cited by 38
RetractedRecent molecular approaches to understanding astrocyte function in vivo
Davila, D., Thibault, K., Fiacco, T. A., & Agulhon, C. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00272 · Cited by 42
Chen, S., Lin, M., Tsai, J.-S., He, P.-L., Luo, W., Herschman, H. R., & Li, H. (2019) · Stem Cells Translational Medicine · doi:10.1002/sctm.18-0284 · Cited by 40
Michinaga, S., Inoue, A., Yamamoto, H., Ryu, R., Inoue, A., Mizuguchi, H., & Kōyama, Y. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108182 · Cited by 38
Pham, H., Ramp, A. A., Klonis, N., Ng, S. W., Klopstein, A., Ayers, M., & Orian, J. (2009) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2008.12.010 · Cited by 33
Decoding astrocyte heterogeneity: New tools for clonal analysis
Bribián, A., Figueres‐Oñate, M., Martín-López, E., & López‐Mascaraque, L. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.04.036 · Cited by 44
Kōyama, Y., & Michinaga, S. (2012) · Journal of Pharmacological Sciences · doi:10.1254/jphs.11r13cp · Cited by 38
Morishita, S., Oku, H., Horie, T., Tonari, M., Kida, T., Okubo, A., Sugiyama, T., Takai, S., Hara, H., & Ikeda, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084387 · Cited by 40
Kōyama, Y. (2013) · BioMolecular Concepts · doi:10.1515/bmc-2013-0004 · Cited by 38
Astrocytes in the Traumatic Brain Injury: the Good and the Bad
Yuan, M., & Wu, H. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113943 · Cited by 39
Schaub, N. J., & Gilbert, R. J. (2011) · Journal of Neural Engineering · doi:10.1088/1741-2560/8/4/046026 · Cited by 38
Regeneration Through in vivo Cell Fate Reprogramming for Neural Repair
Tai, W., Xu, X., & Zhang, C. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00107 · Cited by 36
Synemin is expressed in reactive astrocytes and Rosenthal fibers in Alexander disease
Pekny, T., Faiz, M., Wilhelmsson, U., Curtis, M. A., Matěj, R., Skalli, O., & Pekny, M. (2013) · Apmis · doi:10.1111/apm.12088 · Cited by 39
Self-citationMcHugh, P., Rogers, G. R., Loudon, B., Glubb, D. M., Joyce, P. R., & Kennedy, M. A. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21482 · Cited by 36
Hirko, A. C., Dallasen, R., Jomura, S., & Xu, Y. (2008) · Stem Cells · doi:10.1634/stemcells.2008-0075 · Cited by 35
Radulovic, M., Yoon, H., Wu, J., Mustafa, K., Fehlings, M. G., & Scarisbrick, I. A. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.08.021 · Cited by 33
Toyooka, T., Nawashiro, H., Shinomiya, N., & Shima, K. (2011) · Journal of Neurotrauma · doi:10.1089/neu.2010.1520 · Cited by 33
Astrocyte Activation and the Calcineurin/NFAT Pathway in Cerebrovascular Disease
Kraner, S. D., & Norris, C. M. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00287 · Cited by 33
Corrêa, M. G., Bittencourt, L. O., Nascimento, P. C., Ferreira, R. D. O., Aragão, W. A. B., da Silva, M. C. F., Gomes‐Leal, W., Fernandes, M. D. S., Dionizio, A. S., Buzalaf, M. A. R., et al. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2019.110159 · Cited by 33
Capacity of astrocytes to promote axon growth in the injured mammalian central nervous system
Hemati-Gourabi, M., Cao, T., Romprey, M. K., & Chen, M. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.955598 · Cited by 32
Bone marrow stromal cells reduce ischemia-induced astrocytic activation in vitro
Gao, Q., Li, Y., Shen, L., Zhang, J., Zheng, X. M., Qu, R., Liu, Z., & Chopp, M. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2007.10.069 · Cited by 33
Deplete and repeat: microglial CSF1R inhibition and traumatic brain injury
Boland, R., & Kokiko‐Cochran, O. N. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1352790 · Cited by 32
Metabotropic glutamate receptor-mediated signaling in neuroglia
Loane, D., Stoica, B., & Faden, A. (2012) · Wiley interdisciplinary reviews. Membrane transport and signaling · doi:10.1002/wmts.30 · Cited by 31
Endothelin-1 and endothelin receptors in light-induced retinal degeneration
Torbidoni, V., Iribarne, M., Ogawa, L., Prasanna, G., & Suburo, Á. M. (2005) · Experimental Eye Research · doi:10.1016/j.exer.2004.12.024 · Cited by 32
Yuan, Y., Liu, H., Dai, Z., He, C., Qin, S., & Su, Z. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01258-3 · Cited by 37
Lesion-remote astrocytes govern microglia-mediated white matter repair
McCallum, S. E., Suresh, K. B., Islam, T. S., Tripathi, M. K., Saustad, A. W., Shelest, O., Patil, A., Lee, D. S., Kwon, B., Leitholf, K., et al. (2025) · Nature · doi:10.1038/s41586-025-09887-y · Cited by 36
Glial cell changes in epilepsy: Overview of the clinical problem and therapeutic opportunities
Hubbard, J. A., Hsu, M. S., Fiacco, T. A., & Binder, D. K. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.01.017 · Cited by 31
Gill, S., Hou, Y., Ghane, T., & Pulido, O. M. (2008) · Marine Drugs · doi:10.3390/md6010025 · Cited by 31
Pathologic Potential of Astrocytic Vesicle Traffic: New Targets to Treat Neurologic Diseases?
Vardjan, N., Verkhratsky, A., & Zorec, R. (2015) · Cell Transplantation · doi:10.3727/096368915x687750 · Cited by 32
Yeh, C., Verkhratsky, A., Terzieva, S., & Rodriguez, J. J. (2013) · Biogerontology · doi:10.1007/s10522-013-9456-1 · Cited by 30
Chen, M., Puschmann, T. B., Marášek, P., Inagaki, M., Pekna, M., Wilhelmsson, U., & Pekny, M. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0759-0 · Cited by 30
Self-citationVimentin is required for normal accumulation of body fat
Wilhelmsson, U., Stillemark-Billton, P., Borén, J., & Pekny, M. (2019) · Biological Chemistry · doi:10.1515/hsz-2019-0170 · Cited by 30
Self-citationThe Investigation into Neurotoxicity Mechanisms of Nonylphenol: A Narrative Review
Lotfi, M., Hasanpour, A., Moghadamnia, A. A., & Kazemi, S. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666201119160347 · Cited by 30
Cheon, S. Y., Cho, K., Song, J., & Kim, G. W. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13175 · Cited by 30
Emerging cellular themes in leukodystrophies
Nowacki, J. C., Fields, A. M., & Fu, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.902261 · Cited by 29
Heterogeneity of Astrocyte Reactivity
Clayton, B. L. L., & Liddelow, S. A. (2025) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-112723-031738 · Cited by 33
Hippert, C., Graca, A. B., Basche, M., Kalargyrou, A. A., Georgiadis, A., Ribeiro, J., Matsuyama, A., Aghaizu, N. D., Bainbridge, J. W., Smith, A. J., et al. (2021) · Glia · doi:10.1002/glia.24034 · Cited by 29
Desclaux, M., Perrin, F. E., Do-Thi, A., Prieto-Cappellini, M., y Ribotta, M. G., Mallet, J. J., & Privat, A. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23468 · Cited by 29
Andersson, D., Wilhelmsson, U., Nilsson, M., Kubista, M., Ståhlberg, A., Pekna, M., & Pekny, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070699 · Cited by 29
Self-citationXia, Y., Zhao, T., Li, J., Li, L., Hu, R., Hu, S., Feng, H., & Lin, J. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.10.024 · Cited by 29
Self-citationGenetic targeting of astrocytes to combat neurodegenerative disease
Kirschen, G., Kéry, R., & Chen, A. F. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.265541 · Cited by 29
Chen, X., Xu, C., Liang, H., Xi, Z., Pan, J., Yang, Y., Sun, Q., Yang, G., Sun, Y., & Bian, L. (2020) · Aging · doi:10.18632/aging.103025 · Cited by 28
Wang, Y., Sun, M., Hou, Q., & Hamilton, K. A. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12137 · Cited by 28
Guo, Y., Du, M., Li, R., Li, K., Huang, X., Duan, D., Ai, X., Yao, F., Zhang, L., Hu, Z., et al. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.04.008 · Cited by 28
Cherait, A., Maucotel, J., Lefranc, B., Leprince, J., & Vaudry, D. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.585082 · Cited by 27
Iribarne, M., Ogawa, L., Torbidoni, V., Dodds, C. M., Dodds, R. A., & Suburo, Á. M. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.070605 · Cited by 27
Content and traffic of taurine in hippocampal reactive astrocytes
Junyent, F., de Lemos, L., Utrera, J., Paco, S., Aguado, F., Camins, A., Pallàs, M., Romero, R., & Auladell, C. (2010) · Hippocampus · doi:10.1002/hipo.20739 · Cited by 27
Quantitative 3-D analysis of GFAP labeled astrocytes from fluorescence confocal images
Kulkarni, P. M., Barton, E. A., Savelonas, M. A., Padmanabhan, R., Lu, Y., Trett, K., Shain, W. G., Leasure, J. L., & Roysam, B. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.02.014 · Cited by 26
Lončarević‐Vasiljković, N., Pešić, V., Tanić, N., Milanović, D., Popić, J., Kanazir, S., & Ruždijić, S. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.08.024 · Cited by 26
Neuroprotective effect of 4-(Phenylsulfanyl)butan-2-one on optic nerve crush model in rats
Chien, J.-Y., Sheu, J., Wen, Z., Tsai, R., & Huang, S. (2015) · Experimental Eye Research · doi:10.1016/j.exer.2015.10.004 · Cited by 26
Michinaga, S., Tanabe, A., Nakaya, R., Fukutome, C., Inoue, A., Iwane, A., Minato, Y., Tujiuchi, Y., Miyake, D., Mizuguchi, H., et al. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.14957 · Cited by 25
Ahmadpour, D., & Grange‐Messent, V. (2020) · Neuroendocrinology · doi:10.1159/000509218 · Cited by 22
Ethyl pyruvate promotes spinal cord repair by ameliorating the glial microenvironment
Yuan, Y., Su, Z., Pu, Y., Liu, X., Chen, J., Zhu, F., Zhu, Y., Zhang, H., & He, C. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01804.x · Cited by 25
Michinaga, S., Nagase, M., Matsuyama, E., Yamanaka, D., Seno, N., Fuka, M., Yamamoto, Y., & Kōyama, Y. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102009 · Cited by 24
Multiple Implants Do Not Aggravate the Tissue Reaction in Rat Brain
Lind, G., Gällentoft, L., Danielsen, N., Schouenborg, J., & Pettersson, L. M. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047509 · Cited by 24
Luna, R. I. M., Ku, R. Y., Aruck, A. M., Santiago, F. N., Viczian, A. S., Mauro, D. S., & Zuber, M. E. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.03.005 · Cited by 24
Báez-Jurado, E., Hidalgo‐Lanussa, O., Guio-Vega, G. P., Ashraf, G. M., Echeverría, V., Aliev, G., & Barreto, G. E. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0771-4 · Cited by 25
Yoshii, Y., Otomo, A., Pan, L., Ohtsuka, M., & Hadano, S. (2011) · Neuroscience Research · doi:10.1016/j.neures.2011.03.006 · Cited by 23
Vimentin Phosphorylation Is Required for Normal Cell Division of Immature Astrocytes
de Pablo, Y., Marášek, P., Pozo-Rodrigálvarez, A., Wilhelmsson, U., Inagaki, M., Pekna, M., & Pekny, M. (2019) · Cells · doi:10.3390/cells8091016 · Cited by 23
Self-citationMichinaga, S., Inoue, A., Sonoda, K., Mizuguchi, H., & Kōyama, Y. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105042 · Cited by 23
Treadmill running protects spinal cord contusion from secondary degeneration
de Andrade, M. S. R., de Mendonça, L. M. F., & Chadi, G. (2010) · Brain Research · doi:10.1016/j.brainres.2010.05.070 · Cited by 23
Krylov, A., Yu, S., Veen, K., Newton, A. H., Ye, A., Qin, H., He, J., & Jusuf, P. R. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1087136 · Cited by 19
Ando, T., Sato, S., Toyooka, T., Kobayashi, H., Nawashiro, H., Ashida, H., & Obara, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051744 · Cited by 22
RNA Nanotherapeutics for the Amelioration of Astroglial Reactivity
Smith, J. A., Braga, A., Verheyen, J., Basilico, S., Bandiera, S., Alfaro‐Cervelló, C., Peruzzotti‐Jametti, L., Shu, D., Haque, F., Guo, P., et al. (2017) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2017.11.008 · Cited by 22
Kōyama, Y., Sumie, S., Nakano, Y., Nagao, T., Tokumaru, S., & Michinaga, S. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005614 · Cited by 24
Mechanisms of Dietary Restriction in Aging and Disease
Mobbs, C. V., Yen, K., & Hof, P. R. (2006) · Interdisciplinary topics in gerontology · doi:10.1159/isbn.978-3-318-01390-0 · Cited by 33
Astrocyte phenotypes: Emphasis on potential markers in neuroinflammation.
Bozic, I. D., Savić, D. Z., & Lavrnja, I. C. (2021) · PubMed · doi:10.14670/hh-18-284 · Cited by 22
Mustafa, H. N., & Hussein, A. M. (2015) · Folia Morphologica · doi:10.5603/fm.a2015.0076 · Cited by 21
Dynamic diffusion tensor imaging of spinal cord contusion: A canine model
Liu, C., Yang, D., Li, J., Li, D., Yang, M., Sun, W., Meng, Q., Zhang, W., Cai, C., Du, L., et al. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24222 · Cited by 21
Israelsson, C., Lewén, A., Kylberg, A., Usoskin, D., Althini, S., Lindeberg, J., Deng, C., Fukuda, T., Wang, Y., Kaartinen, V., et al. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20856 · Cited by 20
Acute Astrocyte Activation in Brain Detected by Mri: New Insights into T 1 Hypointensity
Sibson, N. R., Lowe, J. P., Blamire, A. M., Martin, M. J., Obrenovitch, T. P., & Anthony, D. C. (2007) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600549 · Cited by 20
Gomi, H., Yokoyama, T., & Itohara, S. (2009) · Brain Research · doi:10.1016/j.brainres.2009.11.025 · Cited by 19
Vimentin Regulates Neuroplasticity in Transected Spinal Cord Rats Associated with micRNA138
Qian, B.-J., You, L., Shang, F.-F., Liu, J., Dai, P., Lin, N., He, M., Liu, R., Zhang, Y., Xu, Y., et al. (2015) · Molecular Neurobiology · doi:10.1007/s12035-014-8745-2 · Cited by 16
Clasadonte, J., & Haydon, P. G. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0046 · Cited by 19
Endothelin receptors in the detached retina of the pig
Iandiev, I., Uhlmann, S., Pietsch, U., Biedermann, B., Reichenbach, A., Wiedemann, P., & Bringmann, A. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.04.056 · Cited by 19
Mutoji, K. N., Sun, M., Nash, A., Puri, S., Hascall, V., & Coulson‐Thomas, V. J. (2021) · BMC Immunology · doi:10.1186/s12865-021-00443-7 · Cited by 18
Roles of Astrocytic Endothelin ETB Receptor in Traumatic Brain Injury
Michinaga, S., Hishinuma, S., & Kōyama, Y. (2023) · Cells · doi:10.3390/cells12050719 · Cited by 18
Targeting astrocytes in brain injuries: A translational research approach
Barreto, G. E. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.09.001 · Cited by 18
Dixon, K. J., Munro, K. M., Boyd, A., Bartlett, P. F., & Turnley, A. M. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.07.023 · Cited by 18
Michinaga, S., Seno, N., Fuka, M., Yamamoto, Y., Minami, S., Kimura, A., Hatanaka, S., Nagase, M., Matsuyama, E., Yamanaka, D., et al. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13020 · Cited by 17
Astrocyte Mitochondria in White-Matter Injury
Nguyen, H., Zerimech, S., & Baltan, S. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03239-8 · Cited by 18
Astrocyte Responses to Complement Peptide C3a are Highly Context-Dependent
Pekna, M., Siqin, S., de Pablo, Y., Stokowska, A., Naluai, Å. T., & Pekny, M. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03743-5 · Cited by 17
Self-citationIsoflurane does not cause neuroapoptosis but reduces astroglial processes in young adult mice
Dallasen, R., Bowman, J. D., & Xu, Y. (2011) · Medical Gas Research · doi:10.1186/2045-9912-1-27 · Cited by 17
The neurobiology of brain injury.
Pekna, M., & Pekny, M. (2012) · Europe PMC (PubMed Central) · Cited by 17
Self-citationReichenbach, A., & Bringmann, A. (2015) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00122ed1v01y201412ngl003 · Cited by 18
Linberg, K. A., Lewis, G. P., Matsumoto, B., & Fisher, S. K. (2006) · PubMed · Cited by 17
Sitovskaya, D. A., Zabrodskaya, Y., Паршаков, П. А., Sokolova, T., Kudlay, D. A., Starshinova, A. A., & Samochernykh, K. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914490 · Cited by 16
Long-Lasting Actions of Progesterone Protect the Neonatal Brain Following Hypoxia-Ischemia
Fabres, R. B., Montes, N. L., Camboim, Y. D. M., de Souza, S. K., Nicola, F., Tassinari, I. D., Ribeiro, M. F. M., Netto, C. A., & de Fraga, L. S. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00827-0 · Cited by 16
Zhao, H., Lu, Y., Wang, Y., Han, X., Zhang, Y., Han, B., Wang, T., Li, Y., & Wang, S. (2018) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-170722 · Cited by 15
Excess intracellular ATP causes neuropathic pain following spinal cord injury
Nakajima, N., Ohnishi, Y., Yamamoto, M., Setoyama, D., Imai, H., TAKENAKA, T., Matsumoto, M., Hosomi, K., Saitoh, Y., Furue, H., et al. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04510-z · Cited by 16
New role of astrocytes in neuroprotective mechanisms after ischemic stroke
Xie, X., & Liu, J. (2023) · Arquivos de Neuro-Psiquiatria · doi:10.1055/s-0043-1770352 · Cited by 16
Protocol for Xenium spatial transcriptomics studies using fixed frozen mouse brain sections
Ma, X., Chen, P., Wei, J., Zhang, Y., Chen, C.-E., Zhao, H., Ferguson, D., McGee, A. W., Dai, Z., & Qiu, S. (2024) · STAR Protocols · doi:10.1016/j.xpro.2024.103420 · Cited by 16
Ueno, H., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Takahashi, Y., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2019) · Neural Plasticity · doi:10.1155/2019/8924634 · Cited by 16
Metadata
- Authors
- Wilhelmsson, U., Li, L., Pekna, M., Berthold, C.-H., Blom, S., Eliasson, C., Renner, O., Bushong, E., Ellisman, M., Morgan, T. E., & Pekny, M.
- Affiliations
- University of Gothenburg (SE)
- Spanish National Cancer Research Centre (ES)
- University of California San Diego (US)
- University of Southern California (US)
- ORCID
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2004-05-26
- Volume
- 24
- Issue
- 21
- Pages
- 5016-5021
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6729371
- OpenAlex
- W2166851454
- Cited by
- 455
- References
- 126
- Citations by year
- 2026: 14 · 2025: 13 · 2024: 14 · 2023: 12 · 2022: 24 · 2021: 23 · 2020: 31 · 2019: 22 · 2018: 15 · 2017: 18 · 2016: 15 · 2015: 24 · 2014: 26 · 2013: 27 · 2012: 36
- FWCI
- 14.56
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Gothenburg University Publications Electronic Archive (Gothenburg University) (submittedVersion)
- Funders
- Alzheimer's Association
- Swedish Cancer Foundation
- Svenska Sällskapet för Medicinsk Forskning
- Vetenskapsrådet
- National Institutes of Health (RR 04050)
- National Center for Research Resources (RR 04050, P41RR004050, P41 RR04050)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury and Neurovascular Disturbances
- Keywords
- glial fibrillary acidic protein, vimentin, intermediate filaments, reactive astrocytes, astrocyte hypertrophy, astrocytic processes, nerve regeneration, entorhinal cortex lesion, endothelin B receptor, synaptic regeneration, hippocampus
- MeSH terms
- Animals, Astrocytes, Brain Injuries, Cells, Cultured, Cytoplasm, Glial Fibrillary Acidic Protein, Glutamate-Ammonia Ligase, Hippocampus, Hypertrophy, Mice, Inbred C57BL, Nerve Regeneration, Vimentin, Up-Regulation, Entorhinal Cortex, 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