The DOI matches its Crossref record; 140 of the 141 references it cites were found in a registry or an index.
The complex STATes of astrocyte reactivity: How are they controlled by the JAK-STAT3 pathway?
Open accessAbstract
Astrocytes play multiple important roles in brain physiology. In pathological conditions, they become reactive, which is characterized by morphological changes and upregulation of intermediate filament proteins. Besides these descriptive hallmarks, astrocyte reactivity involves significant transcriptional and functional changes that are far from being fully understood. Most importantly, astrocyte reactivity seems to encompass multiple states, each having a specific influence on surrounding cells and disease progression. These diverse functional states of reactivity must be regulated by subtle signaling networks. Many signaling cascades have been associated with astrocyte reactivity, but among them, the JAK-STAT3 pathway is emerging as a central regulator. In this review, we aim (i) to show that the JAK-STAT3 pathway plays a key role in the control of astrocyte reactivity, (ii) to illustrate that STAT3 is a pleiotropic molecule operating multiple functions in reactive astrocytes, and (iii) to suggest that each specific functional state of reactivity is governed by complex molecular interactions within astrocytes, which converge on STAT3. More research is needed to precisely identify the signaling networks controlling the diverse states of astrocyte reactivity. Only then, we will be able to precisely delineate the therapeutic potential of reactive astrocytes in each neurological disease context.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“strong evidence implicates a pivotal role of STAT3 in regulating astrogliosis and astrocyte reactivity in AD (Ceyzeriat et al., 2016).”
From Complement C3aR Inactivation Attenuates Tau Pathology and Reverses an Immune Network Deregulated in Tauopathy Models and Alzheimer’s Disease (2018) · cites this paper as Ceyzeriat et al., 2016
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
Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases
Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455
Darnell, J. E., Kerr, L. M., & Stark, G. R. (1994) · Science · doi:10.1126/science.8197455 · Cited by 6,080
STATs in cancer inflammation and immunity: a leading role for STAT3
Yu, H., Pardoll, D., & Jove, R. (2009) · Nature reviews. Cancer · doi:10.1038/nrc2734 · Cited by 4,383
Darnell, J. E. (1997) · Science · doi:10.1126/science.277.5332.1630 · Cited by 3,979
Principles of interleukin (IL)-6-type cytokine signalling and its regulation
HEINRICH, P. C., BEHRMANN, I., HAAN, S., HERMANNS, H. M., MÜLLER-NEWEN, G., & SCHAPER, F. (2003) · Biochemical Journal · doi:10.1042/bj20030407 · Cited by 3,272 · cited 6×
“The JAK–STAT3 pathway is inhibited by at least three mechanisms: (i) dephosphorylation of the receptors, JAKs and STAT3 by phosphatases like SHP2, (ii) direct inhibition of JAKs by SOCS proteins and (iii) inhibition of DNA binding by PIAS in the nucleus.”
BackgroundInfluentialBromberg, J. F., Wrzeszczynska, M. H., Devgan, G., Zhao, Y., Pestell, R. G., Albanese, C., & Darnell, J. E. (1999) · Cell · doi:10.1016/s0092-8674(00)81959-5 · Cited by 2,790
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
Autophagy in Human Health and Disease
Choi, A. M. K., Ryter, S. W., & Levine, B. (2013) · New England Journal of Medicine · doi:10.1056/nejmra1205406 · Cited by 2,583
Genomic analysis of reactive astrogliosis
Zamanian, J. L., Xu, L., Foo, L. C., Nouri, N., Zhou, L., Giffard, R. G., & Barres, B. A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.6221-11.2012 · Cited by 2,404
Zhong, Z., Wen, Z., & Darnell, J. E. (1994) · Science · doi:10.1126/science.8140422 · Cited by 2,070
Wen, Z., Zhong, Z., & Darnell, J. E. (1995) · Cell · doi:10.1016/0092-8674(95)90311-9 · Cited by 1,974
Crosstalk in NF-κB Signaling Pathways
Oeckinghaus, A., Hayden, M. S., & Ghosh, S. (2011) · Nature Immunology · doi:10.1038/ni.2065 · Cited by 1,942
Astrocyte scar formation aids central nervous system axon regeneration
Anderson, M. A., Burda, J. E., Ren, Y., Ao, Y., O’Shea, T. M., Kawaguchi, R., Coppola, G., Khakh, B. S., Deming, T. J., & Sofroniew, M. V. (2016) · Nature · doi:10.1038/nature17623 · Cited by 1,851
The JAK-STAT Pathway at Twenty
Stark, G. R., & Darnell, J. E., Jr. (2012) · Immunity · doi:10.1016/j.immuni.2012.03.013 · Cited by 1,577
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
Stattic: a small-molecule inhibitor of STAT3 activation and dimerization
Schust, J., Sperl, B., Hollis, A., Mayer, T. U., & Berg, T. (2006) · Chemistry & Biology · doi:10.1016/j.chembiol.2006.09.018 · Cited by 1,105
Regulation of gliogenesis in the central nervous system by the JAK-STAT signaling pathway.
Bonni, A., Sun, Y., Nadal-Vicens, M., Bhatt, A. S., Frank, D., Rozovsky, I., Stahl, N., Yancopouloš, G., & Greenberg, M. (1997) · Science · doi:10.1126/science.278.5337.477 · Cited by 1,050
Akira, S., Nishio, Y., Inoue, M., Wang, X.-J., We, S., Matsusaka, T., Yoshida, K., Sudo, T., Naruto, M., & Kishimoto, T. (1994) · Cell · doi:10.1016/0092-8674(94)90235-6 · Cited by 1,019
Function of Mitochondrial Stat3 in Cellular Respiration
Wegrzyn, J., Potla, R., Chwae, Y.-J., Sepuri, N. B. V., Zhang, Q., Koeck, T., Derecka, M., Szczepanek, K., Szelag, M., Gornicka, A., et al. (2009) · Science · doi:10.1126/science.1164551 · Cited by 1,014
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
Specific Inhibition of Stat3 Signal Transduction by PIAS3
Chung, C. D., Liao, J., Liu, B., Rao, X., Jay, P., Berta, P., & Shuai, K. (1997) · Science · doi:10.1126/science.278.5344.1803 · Cited by 980
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
JAKs and STATs in immunity, immunodeficiency, and cancer
O'Shea, J. J., Holland, S. M., & Staudt, L. M. (2013) · New England Journal of Medicine · doi:10.1056/nejmra1202117 · Cited by 927
Hol, E. M., & Pekny, M. (2015) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2015.02.004 · Cited by 917
Inhibition of acute lymphoblastic leukaemia by a Jak-2 inhibitor
Meydan, N., Grunberger, T., Dadi, H., Shahar, M., Arpaia, E., Lapidot, Z., Leeder, J. S., Freedman, M. H., Cohen, A., Gazit, A., et al. (1996) · Nature · doi:10.1038/379645a0 · Cited by 896
Serine phosphorylation of STATs
Decker, T., & Kovarik, P. (2000) · Oncogene · doi:10.1038/sj.onc.1203481 · Cited by 887
Synergistic Signaling in Fetal Brain by STAT3-Smad1 Complex Bridged by p300
Nakashima, K., Yanagisawa, M., Arakawa, H., Kimura, N., Hisatsune, T., Kawabata, M., Miyazono, K., & Taga, T. (1999) · Science · doi:10.1126/science.284.5413.479 · Cited by 868
Kim, E. H., Kim, M., Woo, D., Shin, Y., Shin, J., Chang, N., Oh, Y. T., Kim, H., Rheey, J., Nakano, I., et al. (2013) · Cancer Cell · doi:10.1016/j.ccr.2013.04.008 · Cited by 846
Wanner, I. B., Anderson, M. A., Song, B., Levine, J., Fernandez, A., Gray-Thompson, Z., Ao, Y., & Sofroniew, M. V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2121-13.2013 · Cited by 839
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
Stat3 Dimerization Regulated by Reversible Acetylation of a Single Lysine Residue
Yuan, Z.-L., Guan, Y.-J., Chatterjee, D., & Chin, Y. E. (2005) · Science · doi:10.1126/science.1105166 · Cited by 790
Astroglial networks: a step further in neuroglial and gliovascular interactions
Giaume, C., Koulakoff, A., Roux, L., Holcman, D., & Rouach, N. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2757 · Cited by 789
A role for uncoupling protein‐2 as a regulator of mitochondrial hydrogen peroxide generation
Nègre‐Salvayre, A., Hirtz, C., Carrera, G., Cazenave, R., Troly, M., Salvayre, R., Pénicaud, L., & Casteilla, L. (1997) · The FASEB Journal · doi:10.1096/fasebj.11.10.9271366 · Cited by 773
Takizawa, T., Nakashima, K., Namihira, M., Ochiai, W., Uemura, A., Yanagisawa, M., Fujita, N., Nakao, M., & Taga, T. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00101-0 · Cited by 620
Autophagy in Human Health and Disease
Doria, A., Gatto, M., & Punzi, L. (2013) · New England Journal of Medicine · doi:10.1056/nejmc1303158 · Cited by 620
Nakajima, K., Yamanaka, Y., Nakae, K., Kojima, H., Ichiba, M., Kiuchi, N., Kitaoka, T., Fukada, T., Hibi, M., & Hirano, T. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00734.x · Cited by 565
Glial cells in (patho)physiology
Parpura, V., Heneka, M. T., Montana, V., Oliet, S. H. R., Schousboe, A., Haydon, P. G., Stout, R. F., Spray, D. C., Reichenbach, A., Pannicke, T., et al. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07664.x · Cited by 561
The role of STAT3 in autophagy
You, L., Wang, Z., Li, H., Shou, J., Jing, Z., Xie, J., Sui, X., Pan, H., & Han, W. (2015) · Autophagy · doi:10.1080/15548627.2015.1017192 · Cited by 515
Polypeptide signalling to the nucleus through tyrosine phosphorylation of Jak and Stat proteins
Shuai, K., Ziemiecki, A., Wilks, A. F., Harpur, A. G., Sadowski, H. B., Gilman, M. Z., & Darnell, J. E., Jr. (1993) · Nature · doi:10.1038/366580a0 · Cited by 509
Elusive roles for reactive astrocytes in neurodegenerative diseases
Ben Haim, L., Carrillo-de Sauvage, M.-A., Ceyzériat, K., & Escartin, C. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00278 · Cited by 453
Self-citationLive imaging of astrocyte responses to acute injury reveals selective juxtavascular proliferation
Bardehle, S., Krüger, M., Buggenthin, F., Schwausch, J., Ninkovic, J., Clevers, H. C., Snippert, H. J. G., Theis, F. J., Meyer‐Luehmann, M., Bechmann, I., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3371 · Cited by 448
Hes binding to STAT3 mediates crosstalk between Notch and JAK–STAT signalling
Kamakura, S., Oishi, K., Yoshimatsu, T., Nakafuku, M., Masuyama, N., & Gotoh, Y. (2004) · Nature Cell Biology · doi:10.1038/ncb1138 · Cited by 430
Mechanism of Activation of Protein Kinase JAK2 by the Growth Hormone Receptor
Brooks, A. J., Dai, W. H., O’Mara, M. L., Abankwa, D., Chhabra, Y., Pelekanos, R., Gardon, O., Tunny, K. A., Blucher, K. M., Morton, C. J., et al. (2014) · Science · doi:10.1126/science.1249783 · Cited by 421
A positive autoregulatory loop of Jak-STAT signaling controls the onset of astrogliogenesis
He, F., Ge, W., Martinowich, K., Becker-Catania, S. G., Coskun, V., Zhu, W., Wu, H., Castro, D. S., Guillemot, F., Fan, G., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1440 · Cited by 413
Boengler, K., Hilfiker‐Kleiner, D., Heusch, G., & Schulz, R. (2010) · Basic Research in Cardiology · doi:10.1007/s00395-010-0124-1 · Cited by 408
Reactive Glia in the Injured Brain Acquire Stem Cell Properties in Response to Sonic Hedgehog
Sirko, S., Behrendt, G., Johansson, P. A., Tripathi, P., Costa, M. R., Bek, S., Heinrich, C., Tiedt, S., Colak, D., Dichgans, M., et al. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.01.019 · Cited by 399
Stat3 and Stat4: members of the family of signal transducers and activators of transcription.
Zhong, Z., Wen, Z., & Darnell, J. E. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.11.4806 · Cited by 397
Reich, N. C., & Liu, L. (2006) · Nature Reviews Immunology · doi:10.1038/nri1885 · Cited by 376
Structure, function, and regulation of STAT proteins
Lim, C. P., & Cao, X. (2006) · Molecular BioSystems · doi:10.1039/b606246f · Cited by 371
Roles of unphosphorylated STATs in signaling
Yang, J., & Stark, G. R. (2008) · Cell Research · doi:10.1038/cr.2008.41 · Cited by 347
Reversible methylation of promoter-bound STAT3 by histone-modifying enzymes
Yang, J., Huang, J., Dasgupta, M., Sears, N., Miyagi, M., Wang, B., Chance, M. R., Chen, X., Du, Y., Wang, Y., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016147107 · Cited by 340
Buffo, A., Rolando, C., & Ceruti, S. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.09.014 · Cited by 338
Ben Haim, L., Ceyzériat, K., Carrillo-de Sauvage, M. A., Aubry, F., Auregan, G., Guillermier, M., Ruiz, M., Petit, F., Houitte, D., Faivre, E., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3516-14.2015 · Cited by 335
JAK-STAT3 pathway regulates spinal astrocyte proliferation and neuropathic pain maintenance in rats
Tsuda, M., Kohro, Y., Yano, T., Tsujikawa, T., Kitano, J., Tozaki‐Saitoh, H., Koyanagi, S., Ohdo, S., Ji, R., Salter, M. W., et al. (2011) · Brain · doi:10.1093/brain/awr025 · Cited by 321
Kershaw, N. J., Murphy, J. M., Liau, N. P. D., Varghese, L. N., Laktyushin, A., Whitlock, E. L., Lucet, I. S., Nicola, N. A., & Babon, J. J. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2519 · Cited by 301
Acquiring signalling specificity from the cytokine receptor gp130
Ernst, M. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.11.003 · Cited by 300
Canonical and non-canonical JAK–STAT signaling
Li, W. X. (2008) · Trends in Cell Biology · doi:10.1016/j.tcb.2008.08.008 · Cited by 300
Cytoplasmic STAT3 represses autophagy by inhibiting PKR activity
Shen, S., Niso-Santano, M., Adjemian, S., Takehara, T., Malik, S. A., Minoux, H., Souquere, S., Mariño, G., Lachkar, S., Senovilla, L., et al. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.09.013 · Cited by 285
Glial 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
Stat3 regulates microtubules by antagonizing the depolymerization activity of stathmin
Ng, D. C. H., Li-n, B., Lim, C. P., Huang, G., Zhang, T., Poli, V., & Cao, X. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200503021 · Cited by 281
Wang, R., Cherukuri, P., & Luo, J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413930200 · Cited by 275
Sriram, K., Benkovic, S. A., Hebert, M. A., Miller, D. B., & O'Callaghan, J. P. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m309304200 · Cited by 265
Song, M., & Ghosh, A. (2004) · Nature Neuroscience · doi:10.1038/nn1192 · Cited by 256
A STAT3-mediated metabolic switch is involved in tumour transformation and STAT3 addiction
Demaria, M., Giorgi, C., Lebiedzińska, M., Esposito, G., D’Angeli, L., Bartoli, A., Gough, D. J., Turkson, J., Levy, D. E., Watson, C. J., et al. (2010) · Aging · doi:10.18632/aging.100232 · Cited by 254
The Jak/STAT pathway is involved in synaptic plasticity
Nicolas, C. S., Peineau, S., Amici, M., Csaba, Z., Fafouri, A., Javalet, C., Collett, V. J., Hildebrandt, L., Seaton, G., Choi, S.-L., et al. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.024 · Cited by 246
Inhibition of IL-6 family cytokines by SOCS3
Babon, J. J., Varghese, L. N., & Nicola, N. A. (2014) · Seminars in Immunology · doi:10.1016/j.smim.2013.12.004 · Cited by 224
STAT3-dependent reactive astrogliosis in the spinal dorsal horn underlies chronic itch
Shiratori‐Hayashi, M., Koga, K., Tozaki‐Saitoh, H., Kohro, Y., Toyonaga, H., Chiharu, Y., Hasegawa, A., Nakahara, T., Hachisuka, J., Akira, S., et al. (2015) · Nature Medicine · doi:10.1038/nm.3912 · Cited by 218
Regulation of STAT signaling by acetylation
Zhuang, S. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.05.007 · Cited by 211
Guo, Z., Jiang, H., Xu, X. Z. S., Duan, W., & Mattson, M. P. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m703753200 · Cited by 202
Diverse functional roles of lipocalin-2 in the central nervous system
Jha, M. K., Lee, S., Park, D. H., Kook, H., Park, K.-G., Lee, I.-K., & Suk, K. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.006 · Cited by 195
Multiple transcription factor families regulate axon growth and regeneration
Moore, D. L., & Goldberg, J. L. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20934 · Cited by 195
Amyloid-β causes memory impairment by disturbing the JAK2/STAT3 axis in hippocampal neurons
Chiba, T., Yamada, M., Sasabe, J., Terashita, K., Shimoda, M., Matsuoka, M., & Aiso, S. (2009) · Molecular Psychiatry · doi:10.1038/mp.2008.105 · Cited by 194
Interleukin-6 signalling: More than Jaks and STATs
Eulenfeld, R., Dittrich, A., Khouri, C., Müller, P. J., Mütze, B., Wolf, A., & Schaper, F. (2012) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2011.09.010 · Cited by 171
Jung, J. E., Kim, G. S., Narasimhan, P., Song, Y. S., & Chan, P. H. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1110-09.2009 · Cited by 169
Tyzack, G. E., Sitnikov, S., Barson, D. G., Adams-Carr, K. L., Lau, N. K., Kwok, J. C. F., Zhao, C., Franklin, R. J. M., Káradóttir, R. T., Fawcett, J. W., et al. (2014) · Nature Communications · doi:10.1038/ncomms5294 · Cited by 169
Braun, D. A., Fribourg, M., & Sealfon, S. C. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.386573 · Cited by 168 · cited 1×
“Computational modeling and experiments on dendritic cells revealed that this could be explained by different temporal profiles of STAT3 activation, resulting in different transcriptional outcomes (Braun et al., 2013).”
BackgroundWang, J., Li, G., Wang, Z., Zhang, X., Yao, L., Wang, F., Liu, S., Yin, J., Ling, E., Wang, L., et al. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.11.062 · Cited by 157
Early Activation of STAT3 Regulates Reactive Astrogliosis Induced by Diverse Forms of Neurotoxicity
O'Callaghan, J. P., Kelly, K. A., VanGilder, R. L., Sofroniew, M. V., & Miller, D. B. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102003 · Cited by 156
Sarafian, T. A., Montes, C., Imura, T., Qi, J., Coppola, G., Geschwind, D. H., & Sofroniew, M. V. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009532 · Cited by 153
Signaling Pathways in Reactive Astrocytes, a Genetic Perspective
Kang, W., & Hébert, J. M. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8163-7 · Cited by 148
Mitochondrial Stat3, the need for design thinking
Yang, R., & Rincon, M. (2016) · International Journal of Biological Sciences · doi:10.7150/ijbs.15153 · Cited by 147
STAT3-driven transcription depends upon the dimethylation of K49 by EZH2
Dasgupta, M., Dermawan, J. K. T., Willard, B. B., & Stark, G. R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503152112 · Cited by 141
Mertens, C., & Darnell, J. E., Jr. (2007) · Cell · doi:10.1016/j.cell.2007.10.033 · Cited by 136
STAT3 signaling after traumatic brain injury
Oliva, A. A., Kang, Y., Sanchez‐Molano, J., Furones, C., & Atkins, C. M. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07610.x · Cited by 134
O'Callaghan, J. P., & Sriram, K. (2004) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2003.12.006 · Cited by 124
The Dark Side of Cell Signaling: Positive Roles for Negative Regulators
Lemmon, M. A., Freed, D. M., Schlessinger, J., & Kiyatkin, A. B. (2016) · Cell · doi:10.1016/j.cell.2016.02.047 · Cited by 120
Kretzschmar, A., Dinger, M., Henze, C., Brocke-Heidrich, K., & Horn, F. (2004) · Biochemical Journal · doi:10.1042/bj20030708 · Cited by 119
A star is born: new insights into the mechanism of astrogenesis
Kanski, R., van Strien, M. E., van Tijn, P., & Hol, E. M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1435-9 · Cited by 119
STAT3 Regulation of Glioblastoma Pathogenesis
de la Iglesia, N., Puram, S. V., & Bonni, A. (2009) · Current Molecular Medicine · doi:10.2174/156652409788488739 · Cited by 117
Translational potential of astrocytes in brain disorders
Verkhratsky, A., Steardo, L., Parpura, V., & Montana, V. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.09.003 · Cited by 115
Multi-tasking: nuclear transcription factors with novel roles in the mitochondria
Szczepanek, K., Lesnefsky, E. J., & Larner, A. C. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.05.001 · Cited by 114
Dynamics and non-canonical aspects of JAK/STAT signalling
Mohr, A., Chatain, N., Domoszlai, T., Rinis, N., Sommerauer, M., Vogt, M., & Müller‐Newen, G. (2011) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2011.09.005 · Cited by 113
Hung, C., Lin, C.-H., Chang, H. H., Wang, C.-Y., Lin, S.-H., Hsu, P.-C., Sun, Y., Lin, T., Shie, F., Kao, L., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3457-15.2016 · Cited by 111
Notch1–STAT3–ETB R signaling axis controls reactive astrocyte proliferation after brain injury
LeComte, M. D., Shimada, I. S., Sherwin, C., & Spees, J. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1501029112 · Cited by 109
STAT3‐Mediated astrogliosis protects myelin development in neonatal brain injury
Nobuta, H., Ghiani, C. A., Paez, P. M., Spreuer, V., Dong, H., Korsak, R. A., Manukyan, A., Li, J., Vinters, H. V., Huang, E. J., et al. (2012) · Annals of Neurology · doi:10.1002/ana.23670 · Cited by 97
The Sin3a repressor complex is a master regulator of STAT transcriptional activity
Icardi, L., Mori, R., Gesellchen, V., Eyckerman, S., Cauwer, L. D., Verhelst, J., Vercauteren, K., Saelens, X., Meuleman, P., Leroux-Roels, G. G., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206458109 · Cited by 96
Escartin, C., Brouillet, E., Gubellini, P., Trioulier, Y., Jacquard, C., Smadja, C., Knott, G. W., Goff, L. K., Déglon, N., Hantraye, P., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0302-06.2006 · Cited by 95
A new minimally-invasive method for microinjection into the mouse spinal dorsal horn
Kohro, Y., Sakaguchi, E., Tashima, R., Tozaki‐Saitoh, H., Okano, H., Inoue, K., & Tsuda, M. (2015) · Scientific Reports · doi:10.1038/srep14306 · Cited by 95
Gao, S. P., & Bromberg, J. (2006) · Science s STKE · doi:10.1126/stke.3432006pe30 · Cited by 92
Gu, Y., He, M., Zhou, X., Liu, J., Hou, N., Tan, B., Zhang, Y., Li, T., & Chen, J. (2016) · Scientific Reports · doi:10.1038/srep18587 · Cited by 89
Linossi, E. M., & Nicholson, S. E. (2015) · Immunological Reviews · doi:10.1111/imr.12305 · Cited by 86
Choi, J., Kim, S.-Y., Cha, J., Choi, Y., Sung, K.-W., Oh, S. T., Kim, O. N., Chung, J. W., Chun, M., Lee, S. B., et al. (2003) · Glia · doi:10.1002/glia.10186 · Cited by 85
Hutchins, A. P., Díez, D., Takahashi, Y., Ahmad, S., Jauch, R., Tremblay, M. L., & Miranda‐Saavedra, D. (2013) · Nucleic Acids Research · doi:10.1093/nar/gks1300 · Cited by 80
Role of Signal Transducer and Activator of Transcription-3 in Up-Regulation of GFAP After Epilepsy
Xu, Z., Xue, T., Zhang, Z., Wang, X., Xu, P., Zhang, J., Lei, X., Li, Y., Xie, Y., Wang, L., et al. (2011) · Neurochemical Research · doi:10.1007/s11064-011-0576-1 · Cited by 77
PI3K Signaling and Stat92E Converge to Modulate Glial Responsiveness to Axonal Injury
Doherty, J., Sheehan, A. E., Bradshaw, R., Fox, A. N., Lu, T.-Y., & Freeman, M. R. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001985 · Cited by 77
Levine, J., Kwon, E., Paez, P., Yan, W., Czerwieniec, G., Loo, J. A., Sofroniew, M. V., & Wanner, I. (2016) · Glia · doi:10.1002/glia.22953 · Cited by 76
Local axonal function of STAT3 rescues axon degeneration in the pmn model of motoneuron disease
Selvaraj, B. T., Frank, N., Bender, F. L. P., Asan, E., & Sendtner, M. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201203109 · Cited by 74
Gautron, L., Lafon, P., Chaigniau, M., Tramu, G., & Layé, S. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00115-x · Cited by 74
Hristova, M., Rocha‐Ferreira, E., Fontana, X., Thei, L., Buckle, R., Christou, M., Hompoonsup, S., Gostelow, N., Raivich, G., & Peebles, D. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13490 · Cited by 74
Colodner, K. J., & Feany, M. Β. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2491-10.2010 · Cited by 71
Acarín, L., Gonz�lez, B., & Castellano, B. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.2.151 · Cited by 70
Washburn, K. B., & Neary, J. T. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.06.034 · Cited by 68
Kim, Y. H., Chung, J.-I., Woo, H. G., Jung, Y., Lee, S., Moon, C., Suh‐Kim, H., & Baik, E. J. (2010) · Stem Cells · doi:10.1002/stem.511 · Cited by 68
Liu, X., Tian, Y., Lu, N., Gin, T., Cheng, C. H. K., & Chan, M. T. V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075804 · Cited by 66
Raymond, M., Li, P., Mangin, J., Huntsman, M. M., & Gallo, V. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3179-11.2011 · Cited by 62
Choi, J., Kim, S.-Y., Park, H.-J., Cha, J., Choi, Y., Kang, J.-E., Chung, J.-W., Chun, M., & Lee, M. (2003) · Molecular Brain Research · doi:10.1016/j.molbrainres.2003.08.010 · Cited by 59
de Castro, G. M., Deja, N. A., Ma, D., Zhao, C., & Franklin, R. J. M. (2015) · American Journal Of Pathology · doi:10.1016/j.ajpath.2015.05.011 · Cited by 59
Xia, X. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1180 · Cited by 58
Ozog, M. A., Bernier, S. M., Bates, D. C., Chatterjee, B., Lo, C. W., & Naus, C. C. G. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-03-0271 · Cited by 57
Reuß, B., Hertel, M., Werner, S., & Unsicker, K. (2000) · Glia · doi:10.1002/(sici)1098-1136(200005)30:3 · Cited by 52
Enhancement of Hypothalamic STAT3 Acetylation by Nuclear Receptor Nur77 Dictates Leptin Sensitivity
Chen, Y., Wu, R., Chen, H., Xiao, Q., Wang, W., He, J., Li, X., Yu, X., Li, L., Wang, P., et al. (2015) · Diabetes · doi:10.2337/db14-1206 · Cited by 51
JAK‐STAT signaling pathway mediates astrogliosis in brains of scrapie‐infected mice
Na, Y., Jin, J., Kim, J., Choi, E., Carp, R. I., & Kim, Y. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04769.x · Cited by 50
Shibata, N., Yamamoto, T., Hiroi, A., Omi, Y., Kato, Y., & Kobayashi, M. (2009) · Neuropathology · doi:10.1111/j.1440-1789.2009.01078.x · Cited by 47
Genetic approaches to study glial cells in the rodent brain
Pfrieger, F. W., & Ślęzak, M. (2011) · Glia · doi:10.1002/glia.22283 · Cited by 47
Transgenic analysis of GFAP promoter elements
Yeo, S., Bandyopadhyay, S., Messing, A., & Brenner, M. (2013) · Glia · doi:10.1002/glia.22536 · Cited by 43
Shibata, N., Kakita, A., Takahashi, H., Ihara, Y., Nobukuni, K., Fujimura, H., Sakoda, S., Sasaki, S., Iwata, M., Morikawa, S., et al. (2009) · Neurodegenerative Diseases · doi:10.1159/000213762 · Cited by 43
Eufemi, M., Cocchiola, R., Romaniello, D., Correani, V., Di Francesco, L., Fabrizi, C., Maras, B., & Schininà, M. E. (2015) · Neurochemistry International · doi:10.1016/j.neuint.2015.01.007 · Cited by 39
Lapp, D. W., Zhang, S. S.-M., & Barnstable, C. J. (2013) · Glia · doi:10.1002/glia.22594 · Cited by 39
Li, L., & Shaw, P. E. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606940200 · Cited by 38
Ignarro, R. S., Vieira, A. S., Sartori, C., Langone, F., Rogerio, F., & Parada, C. (2013) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2013.02.005 · Cited by 29
Zhang, S., Li, W., Wang, W., Zhang, S. S.-M., Huang, P. C., & Zhang, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055683 · Cited by 28
Redox regulation of Janus kinase
Duhé, R. J. (2013) · JAK-STAT · doi:10.4161/jkst.26141 · Cited by 26
Signal transducer and activator of transcription 3 regulation by novel binding partners
Matsuda, T. (2015) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v6.i4.324 · Cited by 19
Lu, J., Power, C., Blevins, G., Giuliani, F., & Yong, V. W. (2013) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000011 · Cited by 18
Moravcová, S., Červená, K., Pačesová, D., & Bendová, Z. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23673 · Cited by 17
Disrupted nuclear import-export in neurodegeneration
Cruz, S. D., & Cleveland, D. W. (2016) · Science · doi:10.1126/science.aad9872 · Cited by 17
Schubert, K. O., Naumann, T., Schnell, O., Zhi, Q., Steup, A., Hofmann, H., & Kirsch, M. (2005) · Experimental Brain Research · doi:10.1007/s00221-005-2330-x · Cited by 13
Overexpression of SCLIP promotes growth and motility in glioblastoma cells
Zhang, Y., Ni, S., Huang, B., Wang, L., Zhang, X., Li, X., Wang, H., Liu, S., Hao, A., & Li, X. (2014) · Cancer Biology & Therapy · doi:10.4161/15384047.2014.987037 · Cited by 12
Gäbel, K., Bednorz, N. L., Klemmt, P. A. B., Vafaizadeh, V., Borghouts, C., & Groner, B. (2009) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci.2010.017 · Cited by 3
Cited by
Sorted by citations
Neuroinflammation in neurodegenerative disorders: the roles of microglia and astrocytes
Kwon, H. S., & Koh, S.-H. (2020) · Translational Neurodegeneration · doi:10.1186/s40035-020-00221-2 · Cited by 2,595
Reactive Astrocytes: Production, Function, and Therapeutic Potential
Liddelow, S. A., & Barres, B. A. (2017) · Immunity · doi:10.1016/j.immuni.2017.06.006 · Cited by 2,336
Function and therapeutic value of astrocytes in neurological diseases
Lee, H.-G., Wheeler, M. A., & Quintana, F. J. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00390-x · Cited by 662
The Role of Astrocytes in CNS Inflammation
Giovannoni, F., & Quintana, F. J. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.007 · Cited by 681
Functional roles of reactive astrocytes in neuroinflammation and neurodegeneration
Patani, R., Hardingham, G. E., & Liddelow, S. A. (2023) · Nature Reviews Neurology · doi:10.1038/s41582-023-00822-1 · Cited by 531
Metadata
- Authors
- Ceyzériat, K., Abjean, L., Carrillo-de Sauvage, M.-A., Ben Haim, L., & Escartin, C.
- Affiliations
- Université Paris-Sud (FR)
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 2016-08
- Volume
- 330
- Pages
- 205-218
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2400419369
- Cited by
- 185
- References
- 141
- Citations by year
- 2026: 14 · 2025: 19 · 2024: 18 · 2023: 30 · 2022: 22 · 2021: 25 · 2020: 19 · 2019: 16 · 2018: 14 · 2017: 8
- FWCI
- 1.27
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- Funders
- Agence Nationale de la Recherche (ANR-10-JCJC-1402, 2011-BSV4-021-03)
- Centre National de la Recherche Scientifique
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- astrocyte activation, JAK/STAT3 signaling, STAT3, reactive astrocytes, intermediate filament proteins, neurological disorders
- MeSH terms
- Animals, Astrocytes, Humans, Signal Transduction, STAT3 Transcription Factor, Janus Kinases
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