The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors
Open accessAbstract
In the developing central nervous system (CNS), the control of synapse number and function is critical to the formation of neural circuits. We previously demonstrated that astrocyte-secreted factors powerfully induce the formation of functional excitatory synapses between CNS neurons. Astrocyte-secreted thrombospondins induce the formation of structural synapses, but these synapses are postsynaptically silent. Here we use biochemical fractionation of astrocyte-conditioned medium to identify glypican 4 (Gpc4) and glypican 6 (Gpc6) as astrocyte-secreted signals sufficient to induce functional synapses between purified retinal ganglion cell neurons, and show that depletion of these molecules from astrocyte-conditioned medium significantly reduces its ability to induce postsynaptic activity. Application of Gpc4 to purified neurons is sufficient to increase the frequency and amplitude of glutamatergic synaptic events. This is achieved by increasing the surface level and clustering, but not overall cellular protein level, of the GluA1 subunit of the AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid) glutamate receptor (AMPAR). Gpc4 and Gpc6 are expressed by astrocytes in vivo in the developing CNS, with Gpc4 expression enriched in the hippocampus and Gpc6 enriched in the cerebellum. Finally, we demonstrate that Gpc4-deficient mice have defective synapse formation, with decreased amplitude of excitatory synaptic currents in the developing hippocampus and reduced recruitment of AMPARs to synapses. These data identify glypicans as a family of novel astrocyte-derived molecules that are necessary and sufficient to promote glutamate receptor clustering and receptivity and to induce the formation of postsynaptically functioning CNS synapses.
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
“In the developing brain, astrocytes regulate synapse number by secreting synaptogenic signals, such as thrombospondins, hevin, and glypicans, that induce synapse formation (Allen et al., 2012; Christopherson et al., 2005; Kucukdereli et al., 2011)”
From The aging astrocyte transcriptome from multiple regions of the mouse brain. (2018) · cites this paper as Allen et al., 2012
In the citing paper
“In line with this, Gpc4 and Gpc6 were recently also discovered as astrocytic factors, which stimulate the excitatory synapse formation by regulating glutamate receptor clustering57.”
From Elimination of the four extracellular matrix molecules tenascin-C, tenascin-R, brevican and neurocan alters the ratio of excitatory and inhibitory synapses (2019) · cites this paper as [57]
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
Glutamate Receptor Ion Channels: Structure, Regulation, and Function
Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Self-citationAMPA Receptor Trafficking and Synaptic Plasticity
Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588
Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis
Christopherson, K. S., Ullian, E. M., Stokes, C. C. A., Mullowney, C. E., Hell, J. W., Agah, A., Lawler, J., Mosher, D. F., Bornstein, P., & Barres, B. A. (2005) · Cell · doi:10.1016/j.cell.2004.12.020 · Cited by 1,688
Self-citationControl of Synapse Number by Glia
Ullian, E. M., Sapperstein, S. K., Christopherson, K. S., & Barres, B. A. (2001) · Science · doi:10.1126/science.291.5504.657 · Cited by 1,380
Self-citationControl of Synaptic Strength by Glial TNFα
Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C. (2002) · Science · doi:10.1126/science.1067859 · Cited by 1,344
Schaeren‐Wiemers, N., & Gerfin-Moser, A. (1993) · Histochemistry and Cell Biology · doi:10.1007/bf00267823 · Cited by 1,151
Eroglu, Ç., Allen, N. J., Susman, M. W., O'Rourke, N. A., Park, C. Y., Özkan, E., Chakraborty, C., Mulinyawe, S. B., Annis, D. S., Huberman, A. D., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.025 · Cited by 893
Self-citationNeuroligins Determine Synapse Maturation and Function
Varoqueaux, F., Aramuni, G., Rawson, R. L., Mohrmann, R., Missler, M., Gottmann, K., Zhang, W., Südhof, T. C., & Brose, N. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.003 · Cited by 837
Micheva, K. D., & Smith, S. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.014 · Cited by 787
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 764
Molecular regulation of synaptogenesis during associative learning and memory
Nelson, T. J., & Alkon, D. L. (2014) · Brain Research · doi:10.1016/j.brainres.2014.11.054 · Cited by 36
Spencer, J. R., Darbyshire, K. M. E., Boucher, A. A., Kashem, M. A., Long, L. E., McGregor, I. S., Karl, T., & Arnold, J. C. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00015 · Cited by 35
Coles, C. H., Jones, E. Y., & Aricescu, A. R. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.09.007 · Cited by 37
Kayama, T., Suzuki, I., Odawara, A., Sasaki, T., & Ikegaya, Y. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.11.115 · Cited by 35
Establishment and Maintenance of Neural Circuit Architecture
Heckman, E. L., & Doe, C. Q. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1143-20.2020 · Cited by 34
Neuro-Immune Cross-Talk in the Striatum: From Basal Ganglia Physiology to Circuit Dysfunction
Mancini, A., Ghiglieri, V., Parnetti, L., Calabresi, P., & Filippo, M. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.644294 · Cited by 38
The role of extracellular matrix in spinal cord development
Wiese, S., & Faissner, A. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.05.018 · Cited by 36
Effects of Transforming Growth Factor Beta 1 in Cerebellar Development: Role in Synapse Formation
Araújo, A. P. B., Diniz, L. P., Eller, C. M., de Matos, B. G., Martinez, R., & Gomes, F. C. A. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00104 · Cited by 35
Farhy-Tselnicker, I., Boisvert, M., & Allen, N. J. (2014) · Biochemical Society Transactions · doi:10.1042/bst20140166 · Cited by 34
Self-citationAstrocytes and the evolution of the human brain
Robertson, J. M. (2013) · Medical Hypotheses · doi:10.1016/j.mehy.2013.12.004 · Cited by 35
Seducing astrocytes to the dark side
Burda, J. E., & Sofroniew, M. V. (2017) · Cell Research · doi:10.1038/cr.2017.37 · Cited by 34
Pathogenic Variants in GPC4 Cause Keipert Syndrome
Amor, D. J., Stephenson, S. E. M., Mustapha, M., Mensah, M. A., Ockeloen, C. W., Lee, W. S., Tankard, R. M., Phelan, D., Shinawi, M. S., de Brouwer, A. P. M., et al. (2019) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2019.02.026 · Cited by 34
Self-citationControl of neural development and function by glial neuroligins
Sakers, K., & Eroğlu, Ç. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.03.007 · Cited by 33
Singhal, G., Morgan, J., Jawahar, M. C., Corrigan, F., Jaehne, E. J., Toben, C. G., Breen, J., Pederson, S., Manavis, J., Hannan, A. J., et al. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112501 · Cited by 37
Adult and endemic neurogenesis in the vestibular nuclei after unilateral vestibular neurectomy
Rastoldo, G., Mahmoudi, N. E., Marouane, E., Péricat, D., Watabe, I., Toneto, A., López‐Juárez, A., Chabbert, C., & Tighilet, B. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101899 · Cited by 34
Astrocyte‐induced synapse formation and ischemic stroke
Yamagata, K. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24807 · Cited by 34
Sox2 -Deficient Müller Glia Disrupt the Structural and Functional Maturation of the Mammalian Retina
Bachleda, A., Pevny, L., & Weiss, E. R. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-17994 · Cited by 32
The roles of cortical astrocytes in chronic pain and other brain pathologies
Eto, K., Kim, S. K., Takeda, I., & Nabekura, J. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.08.009 · Cited by 32
Middelkamp, H. H. T., Verboven, A. H. A., Vivas, A., Schoenmaker, C., Gunnewiek, T. M. K., Passier, R. C., Albers, C. A., Hoen, P. A. C. ’., Kasri, N. N., & van der Meer, A. D. (2021) · Scientific Reports · doi:10.1038/s41598-021-81933-x · Cited by 32
Chen, L., Yang, N., Li, Y., Li, Y., Hong, J., Wang, Q., Liu, K., Han, D., Han, Y., Mi, X., et al. (2021) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13718 · Cited by 35
Sideris, E., Kioulaphides, S., Wilson, K. L., Yu, A., Chen, J., Carmichael, S. T., & Segura, T. (2022) · Advanced Therapeutics · doi:10.1002/adtp.202200048 · Cited by 30
Dinh, M. L., Koppel, S. J., Korn, M. J., & Cramer, K. S. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.08.016 · Cited by 33
Compartment-Specific Neurexin Nanodomains Orchestrate Tripartite Synapse AssemblyPreprint
Trotter, J. H., Dargaei, Z., Sclip, A., Essayan-Perez, S., Liakath‐Ali, K., Raju, K., Nabet, A., Liu, X., Wöhr, M., & Südhof, T. C. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.21.262097 · Cited by 35
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
Boning up on glypicans—opportunities for new insights into bone biology
Dwivedi, P. P., Lam, N. N., & Powell, B. C. (2013) · Cell Biochemistry and Function · doi:10.1002/cbf.2939 · Cited by 34
Matić, K., Eninger, T., Bardoni, B., Davidovic, L., & Maček, B. (2014) · Journal of Proteome Research · doi:10.1021/pr5006372 · Cited by 33
Control of Cell Shape, Neurite Outgrowth, and Migration by a Nogo-A/HSPG Interaction
Kempf, A., Boda, E., Kwok, J. C. F., Fritz, R. D., Grande, V., Kaelin, A. M., Ristic, Z., Schmandke, A., Schmandke, A., Tews, B., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.08.014 · Cited by 33
Synapse Dysfunctions in Multiple Sclerosis
Schwarz, K., & Schmitz, F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021639 · Cited by 36
Astrocyte glypican 5 regulates synapse maturation and stabilization
Bosworth, A. P., Contreras, M., Sancho, L., Salas, I. H., Paumier, A., Novak, S. W., Manor, U., & Allen, N. J. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115374 · Cited by 32
Self-citationLesion-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
Channels and Transporters in Astrocyte Volume Regulation in Health and Disease
Reed, M., & Blazer‐Yost, B. L. (2022) · Cellular Physiology and Biochemistry · doi:10.33594/000000495 · Cited by 31
Zhang, N., Zhang, Y., Wang, Z., & Chen, N. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-00861-2 · Cited by 31
Koh, S., Kim, N., Yin, H. H., Harris, I. R., Dejneka, N. S., & Eroğlu, Ç. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1364-15.2015 · Cited by 31
The influence of asthma on neuroinflammation and neurodevelopment: From epidemiology to basic models
Tamayo, J. M., Osman, H. C., Schwartzer, J. J., & Ashwood, P. (2023) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2023.12.003 · Cited by 32
Naganuma, F., Yoshikawa, T., Nakamura, T., Iida, T., Harada, R., Mohsen, A. S., Miura, Y., & Yanai, K. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12665 · Cited by 30
Human Primary Astrocytes Differently Respond to Pro- and Anti-Inflammatory Stimuli
Szpakowski, P., Ksiazek-Winiarek, D. J., Turniak, M., Pacan, I., & Glabinski, A. R. (2022) · Biomedicines · doi:10.3390/biomedicines10081769 · Cited by 30
Feng, Y., Yang, L., Ma, X., Huang, Z., Zong, X., Citadin, C. T., Lin, H. W., & Zhang, Q. (2022) · Neurochemistry International · doi:10.1016/j.neuint.2022.105464 · Cited by 30
Electroconvulsive seizure induces thrombospondin-1 in the adult rat hippocampus
Okada‐Tsuchioka, M., Segawa, M., Kajitani, N., Hisaoka‐Nakashima, K., Shibasaki, C., Morinobu, S., & Takebayashi, M. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.10.001 · Cited by 30
Yasui, T., Uezono, N., Nakashima, H., Noguchi, H., Matsuda, T., Noda-Andoh, T., Okano, H., & Nakashima, K. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.05.001 · Cited by 27
Mechanisms of Cortical Differentiation
Adnani, L., Han, S., Li, S., Mattar, P. A., & Schuurmans, C. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.07.005 · Cited by 33
Human Glial Chimeric Mice to Define the Role of Glial Pathology in Human Disease
Mariani, J. N., Zou, L., & Goldman, S. A. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9072-6_18 · Cited by 30
Rupareliya, V. P., Singh, A. A., Butt, A. M., A, H., & Kumar, H. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.176048 · 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
Shu, Q., Hu, Z., Huang, C., Yu, X., Fan, H., Yang, J.-W., Fang, P., Ni, L., Chen, J., & Wang, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0095259 · Cited by 29
Koh, S., Chen, W. J., Dejneka, N. S., Harris, I. R., Lü, B., Girman, S., Saylor, J., Wang, S., & Eroğlu, Ç. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1532-17.2018 · Cited by 29
Testen, A., Ali, M., Sexton, H. G., Hodges, S., Dubester, K., Reissner, K. J., Swartzwelder, H. S., & Risher, M.-L. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2018.12.044 · Cited by 29
Cognitive complications of cancer and cancer-related treatments – Novel paradigms
Lomeli, N., Lepe, J. J., Gupta, K., & Bota, D. A. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135720 · Cited by 35
The HSPG syndecan is a core organizer of cholinergic synapses
Zhou, X., Vachon, C., Cizeron, M., Romatif, O., Bülow, H. E., Jospin, M., & Bessereau, J. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202011144 · Cited by 31
Sox2 regulates astrocytic and vascular development in the retina
Kautzman, A. G., Keeley, P. W., Nahmou, M. M., Luna, G., Fisher, S. K., & Reese, B. E. (2017) · Glia · doi:10.1002/glia.23269 · Cited by 28
Mixed-species RNA-seq for elucidation of non-cell-autonomous control of gene transcription
Qiu, J. L., Dando, O., Baxter, P. S., Hasel, P., Heron, S., Simpson, T. I., & Hardingham, G. E. (2018) · Nature Protocols · doi:10.1038/s41596-018-0029-2 · Cited by 30
The function of glypicans in the mammalian embryo
Filmus, J. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00045.2022 · Cited by 28
Astrocytes regulate neuronal network activity by mediating synapse remodeling
Kim, N., & Chung, W. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.09.007 · Cited by 31
Alterations of the blood-brain barrier during aging
Cao, Y., Xu, W., & Liu, Q. (2024) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x241240843 · Cited by 30
Impact of maternal immune activation on dendritic spine development
Pękała, M., Doliwa, M., & Kalita, K. B. (2020) · Developmental Neurobiology · doi:10.1002/dneu.22804 · Cited by 27
Astrocyte-Derived Thrombospondin Induces Cortical Synaptogenesis in a Sex-Specific Manner
Mazur, A., Bills, E., DeSchepper, K. M., Williamson, J. C., Henderson, B. J., & Risher, W. C. (2021) · eNeuro · doi:10.1523/eneuro.0014-21.2021 · Cited by 29
Astrocyte adaptation in Alzheimer’s disease: a focus on astrocytic P2X7R
Beltran-Lobo, P., Reid, M. J., Jiménez-Sánchez, M., Verkhratsky, A., Perez‐Nievas, B. G., & Noble, W. J. (2022) · Essays in Biochemistry · doi:10.1042/ebc20220079 · Cited by 30
Glia: guardians, gluttons, or guides for the maintenance of neuronal connectivity?
Jebelli, J. D., Su, W., Hopkins, S., Pocock, J. M., & Garden, G. A. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12711 · Cited by 28
Turko, P., Groberman, K., Browa, F., Cobb, S., & Vida, I. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy029 · Cited by 27
Astrocyte growth is driven by the Tre1/S1pr1 phospholipid-binding G protein-coupled receptor
Chen, J., Stork, T., Kang, Y., Nardone, K., Auer, F., Farrell, R. J., Jay, T. R., Heo, D., Sheehan, A. E., Paton, C., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.11.008 · Cited by 27
Systems genetic analysis of hippocampal neuroanatomy and spatial learning in mice
Delprato, A., Bonheur, B., Algéo, M.-P., Rosay, P., Lu, L., Williams, R. W., & Crusio, W. E. (2015) · Genes Brain & Behavior · doi:10.1111/gbb.12259 · Cited by 27
Li, Y., Xie, Y., Liu, R., Wang, Z., Chen, P., Wang, M., Yu, Z., Wang, W., & Luo, X. (2023) · Glia · doi:10.1002/glia.24433 · Cited by 28
Nataf, S., Barritault, M., & Pays, L. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102097 · Cited by 26
Huang, K., & Park, S. (2021) · eNeuro · doi:10.1523/eneuro.0069-21.2021 · Cited by 38
Filmus, J. (2023) · Proteoglycan Research · doi:10.1002/pgr2.5 · Cited by 27
Function and therapeutic value of astrocytes in diabetic cognitive impairment
Meng, F., Fu, J., Zhang, L., Guo, M., Zhuang, P., Yin, Q., & Zhang, Y. (2023) · Neurochemistry International · doi:10.1016/j.neuint.2023.105591 · Cited by 26
Astrocytes and microglia in the coordination of CNS development and homeostasis
Lopez‐Ortiz, A. O., & Eyo, U. B. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.16006 · Cited by 32
Thrombospondins 1 and 2 are important for afferent synapse formation and function in the inner ear
Mendus, D., Sundaresan, S., Grillet, N., Wangsawihardja, F., Leu, R. K., Müller, U., Jones, S. M., & Mustapha, M. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12486 · Cited by 27
miR‐31 mutants reveal continuous glial homeostasis in the adult Drosophila brain
Foo, L. C., Song, S., & Cohen, S. M. (2017) · The EMBO Journal · doi:10.15252/embj.201695861 · Cited by 27
Self-citationCiuba, K., Piotrowska, A., Chaudhury, D., Dehingia, B., Duński, E., Behr, R., Soroczyńska, K., Czystowska-Kuźmicz, M., Abbas, M., Bulanda, E., et al. (2025) · Cell Stem Cell · doi:10.1016/j.stem.2024.12.011 · Cited by 25
Paracrine Role for Somatostatin Interneurons in the Assembly of Perisomatic Inhibitory Synapses
Su, J., Basso, D., Iyer, S., Su, K., Wei, J., & Fox, M. A. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0613-20.2020 · Cited by 26
Astrocyte 3D culture and bioprinting using peptide functionalized hyaluronan hydrogels
Matthiesen, I., Jury, M., Boroojeni, F. R., Ludwig, S. L., Holzreuter, M. A., Buchmann, S., Träger, A., Selegård, R., Winkler, T. E., Aili, D., et al. (2023) · Science and Technology of Advanced Materials · doi:10.1080/14686996.2023.2165871 · Cited by 25
Narayanan, B., Ethridge, L. E., O'Neil, K. M., Dunn, S. M., Mathew, I. T., Tandon, N., Calhoun, V. D., Ruaño, G., Kocherla, M., Windemuth, A., et al. (2015) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2014.13101411 · Cited by 25
Lischka, F. W., Efthymiou, A. G., Zhou, Q., Nieves, M. D., McCormack, N. M., Wilkerson, M. D., Sukumar, G., Dalgard, C. L., & Doughty, M. L. (2017) · Glia · doi:10.1002/glia.23278 · Cited by 25
Regulation of rhythmic behaviors by astrocytes
Jackson, F. R., You, S., & Crowe, L. B. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.372 · Cited by 25
Astrocytes in stroke-induced neurodegeneration: a timeline
Collyer, E., & Blanco‐Suárez, E. (2023) · Frontiers in Molecular Medicine · doi:10.3389/fmmed.2023.1240862 · Cited by 26
The ROP vesicle release factor is required in adult Drosophila glia for normal circadian behavior
Ng, F., & Jackson, F. R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00256 · Cited by 25
Ibi, D., & Yamada, K. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161226092 · Cited by 24
Gunnewiek, T. M. K., Verboven, A. H. A., Pelgrim, I., Hogeweg, M., Schoenmaker, C., Renkema, G. H., Beyrath, J., Smeitink, J. A. M., Vries, B. B. A. D., Hoen, P. A. C. ’., et al. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.07.002 · Cited by 24
The function of astrocytes and their role in neurological diseases
Yuan, W., Huang, W., Jiang, Y., Xu, H., Duan, C., Chen, N., Liu, Y., & Fu, X. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16160 · Cited by 26
Modern approaches to investigating non‐neuronal aspects of Alzheimer's disease
Liddelow, S. A. (2019) · The FASEB Journal · doi:10.1096/fj.201802592 · Cited by 26
A view of the genetic and proteomic profile of extracellular matrix molecules in aging and stroke
Chmelová, M., Androvic, P., Kirdajová, D., Turečková, J., Kriška, J., Valihrach, L., Anděrová, M., & Vargová, L. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1296455 · Cited by 24
Regulation of neuronal axon specification by glia-neuron gap junctions in C. elegans
Meng, L., Zhang, A., Jin, Y., & Yan, D. (2016) · eLife · doi:10.7554/elife.19510 · Cited by 29
Rurak, G. M., Woodside, B. C., Aguilar‐Valles, A., & Salmaso, N. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100897 · Cited by 24
Primary Cilia and Dendritic Spines: Different but Similar Signaling Compartments
Nechipurenko, I. V., Doroquez, D. B., & Sengupta, P. (2013) · Molecules and Cells · doi:10.1007/s10059-013-0246-z · Cited by 23
Zhou, C., Zhang, Y., Xue, F., Xue, S., Chen, Y., Gu, T., Peng, Z., & Wang, H. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7547 · Cited by 23
Hamabe‐Horiike, T., Kawasaki, K., Sakashita, M., Ishizu, C., Yoshizaki, T., Harada, S.-I., Ogawa‐Ochiai, K., Shinmyo, Y., & Kawasaki, H. (2021) · Scientific Reports · doi:10.1038/s41598-021-84210-z · Cited by 23
Li, J., Pan, L., Godoy, M. I., Pembroke, W. G., Rexach, J. E., Condro, M. C., Alvarado, A. G., Harteni, M., Chen, Y.-W., Stiles, L., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.17.044222 · Cited by 23
The contribution of the meningeal immune interface to neuroinflammation in traumatic brain injury
Mokbel, A. Y., Burns, M. P., & Main, B. S. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03122-7 · Cited by 25
Targeting astrocytes polarization after spinal cord injury: a promising direction
Li, H., Liu, Y., Sun, Y., Guo, H., Lv, S., Guo, W., Ren, J., Wang, Y., Zu, J., Yan, J., et al. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1478741 · Cited by 22
Spohr, T. C. L. D. S. E., Dezonne, R. S., Rehen, S. K., & Gomes, F. C. A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00296 · Cited by 22
New strategies for managing adult gliomas
Kirby, A. J., & Finnerty, G. T. (2020) · Journal of Neurology · doi:10.1007/s00415-020-09884-3 · Cited by 23
Presynaptic Proteoglycans: Sweet Organizers of Synapse Development
Song, Y. S., & Kim, E. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.048 · Cited by 21
Xiong, Y., Zhang, Y., Zheng, F., Yang, Y., Xu, X. Y., Wang, W., Zhu, B., & Wang, X. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.07.061 · Cited by 21
Luo, R., Zhou, B., Liao, P. S., Zuo, Y., & Jiang, R. (2023) · Glia · doi:10.1002/glia.24358 · Cited by 21
Luo, D., Li, J., Liu, H., Wang, J., Xia, Y., Qiu, W., Wang, N., Wang, X., Wang, X., Ma, C., et al. (2023) · Advanced Science · doi:10.1002/advs.202300876 · Cited by 20
Qin, L., Liu, Z., Guo, S., Han, Y., Wang, X., Ren, W. T., Chen, J., Zhen, H., Nie, C., Xing, K.-K., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02659-6 · Cited by 23
Role of neuron-glia interactions in developmental synapse elimination
Terni, B., López-Murcia, F. J., & Llobet, A. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.08.017 · Cited by 21
Synaptogenesis Is Modulated by Heparan Sulfate in Caenorhabditis elegans
Lázaro‐Peña, M. I., Díaz-Balzac, C. A., Bülow, H. E., & Emmons, S. W. (2018) · Genetics · doi:10.1534/genetics.118.300837 · Cited by 21
Apóstolo, N., & de Wit, J. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.01.025 · Cited by 23
Matrix metalloproteinase-3 in brain physiology and neurodegeneration
Lech, A. M., Wiera, G., & Mozrzymas, J. W. (2019) · Advances in Clinical and Experimental Medicine · doi:10.17219/acem/110319 · Cited by 24
Metadata
- Authors
- Allen, N. J., Bennett, M. L., Foo, L. C., Wang, G. X., Chakraborty, C., Smith, S. J., & Barres, B. A.
- Affiliations
- Stanford Medicine (US)
- Corresponding author
- Allen, Nicola J.
- ORCID
- Venue
- Nature
- Published
- 2012-05-27
- Volume
- 486
- Issue
- 7403
- Pages
- 410-414
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3383085
- OpenAlex
- W2012935976
- Cited by
- 764
- References
- 32
- Citations by year
- 2026: 49 · 2025: 58 · 2024: 61 · 2023: 72 · 2022: 61 · 2021: 72 · 2020: 64 · 2019: 47 · 2018: 43 · 2017: 56 · 2016: 39 · 2015: 48 · 2014: 46 · 2013: 36 · 2012: 11
- FWCI
- 18.58
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute on Drug Abuse (R01DA015043)
- National Institute of Neurological Disorders and Stroke (R01NS0725252, R01NS075252, R01NS077601)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- GPC4, astrocytes, excitatory synapse formation, retinal ganglion cells, glutamatergic neurotransmission, synaptic plasticity, synaptic dysfunction, astrocyte-neuron interaction, hippocampus
- MeSH terms
- Animals, Astrocytes, Cerebellum, Female, Hippocampus, Humans, Male, Mice, Inbred C57BL, Retinal Ganglion Cells, Synapses, Culture Media, Conditioned, Rats, Sprague-Dawley, Receptors, AMPA, Excitatory Postsynaptic Potentials, Mice, Rats, Glypicans
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