Glia — more than just brain glue

Astrocyte Control of Synaptic Transmission and Neurovascular Coupling

Haydon, P. G., & Carmignoto, G. (2006) · Physiological Reviews · doi:10.1152/physrev.00049.2005 · Cited by 1,371

The Mystery and Magic of Glia: A Perspective on Their Roles in Health and Disease

Barres, B. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.013 · Cited by 1,352

Axon-Glial Signaling and the Glial Support of Axon Function

Nave, K., & Trapp, B. D. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094309 · Cited by 664

The astrocyte odyssey

Wang, D. D., & Bordey, A. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.09.015 · Cited by 538

Signaling between glia and neurons: focus on synaptic plasticity

Allen, N. J., & Barres, B. A. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.08.006 · Cited by 321

Glial cell biology in Drosophila and vertebrates.

Freeman, M., & Doherty, J. E. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2005.12.002 · Cited by 283

Neuroglia

(2004) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195152227.001.0001 · Cited by 59

The Glymphatic System: A Novel Therapeutic Target for Stroke Treatment

Lv, T., Zhao, B., Hu, Q., & Zhang, X. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.689098 · Cited by 107

Ependymal cells of chordate larvae are stem-like cells that form the adult nervous system

Horie, T., Shinki, R., Ogura, Y., Kusakabe, T. G., Satoh, N., & Sasakura, Y. (2010) · Nature · doi:10.1038/nature09631 · Cited by 104

O-GlcNAc transferase in astrocytes modulates depression-related stress susceptibility through glutamatergic synaptic transmission

Fan, J., Guo, F., Mo, R., Chen, L., Mo, J., Lu, C., Ren, J., Zhong, Q., Kuang, X., Wen, Y., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci160016 · Cited by 109

Molecular Profiles of Drinking Alcohol to Intoxication in C57BL/6J Mice

Mulligan, M. K., Rhodes, J. S., Crabbe, J. C., Mayfield, R. D., Harris, R. A., & Ponomarev, I. (2011) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2010.01384.x · Cited by 106

Activation of satellite glial cells in lumbar dorsal root ganglia contributes to neuropathic pain after spinal nerve ligation

Liu, F., Sun, Y., Wang, F.-T., Li, Q., Su, L., Zhao, Z., Meng, X., Zhao, H., Wu, X. L., Sun, Q., et al. (2011) · Brain Research · doi:10.1016/j.brainres.2011.10.016 · Cited by 104

Regulation of Astrocyte Functions in Multiple SclerosisPreprint

Wheeler, M. A., & Quintana, F. J. (2018) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a029009 · Cited by 103

Biphasic Mechanisms of Neurovascular Unit Injury and Protection in CNS Diseases

Maki, T., Hayakawa, K., Pham, L. D., Xing, C., Lo, E. H., & Arai, K. (2013) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527311312030004 · Cited by 103

Detection of early neuron degeneration and accompanying glial responses in the visual pathway in a rat model of acute intraocular hypertension

Zhang, S., Wang, H., Lu, Q., Qing, G., Wang, N., Wang, Y., Li, S., Yang, D., & Yan, F. (2009) · Brain Research · doi:10.1016/j.brainres.2009.09.029 · Cited by 99

Biomarkers for parkinsonian disorders in CNS-originating EVs: promise and challenges

Dutta, S., Hornung, S., Taha, H. B., & Bitan, G. (2023) · Acta Neuropathologica · doi:10.1007/s00401-023-02557-1 · Cited by 103

Progesterone Increases the Release of Brain-Derived Neurotrophic Factor from Glia via Progesterone Receptor Membrane Component 1 (Pgrmc1)-Dependent ERK5 Signaling

Su, C., Cunningham, R. L., Rybalchenko, N., & Singh, M. (2012) · Endocrinology · doi:10.1210/en.2011-2177 · Cited by 101

From the Bottom-Up: Chemotherapy and Gut-Brain Axis Dysregulation

Bajic, J. E., Johnston, I. N., Howarth, G. S., & Hutchinson, M. R. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00104 · Cited by 100

Astrocytic activation in the anterior cingulate cortex is critical for sleep disorder under neuropathic pain

Yamashita, A., Hamada, A., Suhara, Y., Kawabe, R., Yanase, M., Kuzumaki, N., Narita, M., Matsui, R., Okano, H., & Narita, M. (2014) · Synapse · doi:10.1002/syn.21733 · Cited by 98

RNA sequencing analysis reveals quiescent microglia isolation methods from postnatal mouse brains and limitations of BV2 cells

He, Y., Yao, X., Taylor, N., Bai, Y., Lovenberg, T. W., & Bhattacharya, A. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1195-4 · Cited by 111

In VivoImaging of Dorsal Root Regeneration: Rapid Immobilization and Presynaptic Differentiation at the CNS/PNS Border

Maio, A. D., Skuba, A., Himes, B. T., Bhagat, S. L., Hyun, J. K., Tessler, A. R., Bishop, D. L., & Son, Y. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4638-10.2011 · Cited by 99

MicroRNAs and depression

Mouillet‐Richard, S., Baudry, A., Launay, J., & Kellermann, O. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.12.035 · Cited by 98

Astrocytes in the regulation of cerebrovascular functions

Cohen‐Salmon, M., Slaoui, L., Mazaré, N., Gilbert, A., Oudart, M., Alvear‐Perez, R., Elorza‐Vidal, X., Chever, O., & Boulay, A. (2021) · Glia · doi:10.1002/glia.23924 · Cited by 93

Environmental Enrichment Stimulates Immune Cell Secretion of Exosomes that Promote CNS Myelination and May Regulate Inflammation

Pusic, K. M., Pusic, A. D., & Kraig, R. P. (2016) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-015-0269-4 · Cited by 99

Involvement of Aquaporin 4 in Astrocyte Function and Neuropsychiatric Disorders

Xiao, M., & Hu, G. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12267 · Cited by 99

Schizophrenia: susceptibility genes and oligodendroglial and myelin related abnormalities

Roussos, P., & Haroutunian, V. H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00005 · Cited by 97

Coincident Generation of Pyramidal Neurons and Protoplasmic Astrocytes in Neocortical Columns

Magavi, S. S. P., Friedmann, D., Banks, G. P., Stolfi, A., & Lois, C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3560-11.2012 · Cited by 94

Attenuation of pro-inflammatory mediators in LPS-stimulated BV2 microglia by chitooligosaccharides via the MAPK signaling pathway

Pangestuti, R., Bak, S., & Kim, S. (2011) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2011.06.014 · Cited by 93

The secreted neurotrophin Spätzle 3 promotes glial morphogenesis and supports neuronal survival and functionPreprint

Coutinho‐Budd, J., Sheehan, A. E., & Freeman, M. R. (2017) · Genes & Development · doi:10.1101/gad.305888.117 · Cited by 94

Developmental maturation of astrocytes and pathogenesis of neurodevelopmental disorders

Yang, Y., Higashimori, H., & Morel, L. (2013) · Journal of Neurodevelopmental Disorders · doi:10.1186/1866-1955-5-22 · Cited by 99

Cellular and Synaptic Dysfunctions in Parkinson’s Disease: Stepping Out of the Striatum

Mallet, N. P., Delgado-Zabalza, L., Chazalon, M., Miguélez, C., & Baufreton, J. (2019) · Cells · doi:10.3390/cells8091005 · Cited by 98

Isolation Housing Exacerbates Alzheimer's Disease-Like Pathophysiology in Aged APP/PS1 Mice

Huang, H., Wang, L., Cao, M., Marshall, C., Gao, J., Xiao, N., Hu, G., & Xiao, M. (2015) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyu116 · Cited by 94

The interplay of early-life stress, nutrition, and immune activation programs adult hippocampal structure and function

Hoeijmakers, L., Lucassen, P. J., & Kőrösi, A. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00103 · Cited by 98

Role of glia in developmental synapse formation

Allen, N. J. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.06.004 · Cited by 95

Aspects of Astrocyte Energy Metabolism, Amino Acid Neurotransmitter Homoeostasis and Metabolic Compartmentation

Kreft, M., Bak, L. K., Waagepetersen, H. S., & Schousboe, A. (2012) · ASN Neuro · doi:10.1042/an20120007 · Cited by 88

Astrocyte Diversity: Current Insights and Future Directions

Westergard, T., & Rothstein, J. D. (2020) · Neurochemical Research · doi:10.1007/s11064-020-02959-7 · Cited by 90

An Overview on the Differential Interplay Among Neurons–Astrocytes–Microglia in CA1 and CA3 Hippocampus in Hypoxia/Ischemia

Lana, D., Ugolini, F., & Giovannini, M. G. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.585833 · Cited by 92

Rapid manifestation of reactive astrogliosis in acute hippocampal brain slices

Takano, T., He, W. J., Han, X., Wang, F., Xu, Q., Wang, X., Bush, N. A. O., Cruz, N. F., Dienel, G. A., & Nedergaard, M. (2013) · Glia · doi:10.1002/glia.22588 · Cited by 96

Bioinspired Materials for In Vivo Bioelectronic Neural Interfaces

Woods, G. A., Rommelfanger, N. J., & Hong, G. (2020) · Matter · doi:10.1016/j.matt.2020.08.002 · Cited by 89

The multifaceted role of glial cells in amyotrophic lateral sclerosis

Valori, C. F., Brambilla, L., Martorana, F., & Rossi, D. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1429-7 · Cited by 88

Astrocytes in the central nervous system and their functions in health and disease: A review

Gradišnik, L., & Velnar, T. (2023) · World Journal of Clinical Cases · doi:10.12998/wjcc.v11.i15.3385 · Cited by 70

Astrocitos en las enfermedades neurodegenerativas (I): función y caracterización molecular

Guillamón-Vivancos, T., Gómez‐Pinedo, U., & Matías‐Guiu, J. (2013) · Neurología · doi:10.1016/j.nrl.2012.12.007 · Cited by 98

Distinct repertoires of microRNAs present in mouse astrocytes compared to astrocyte-secreted exosomes

Jovičić, A., & Gitler, A. D. (2017) · PLOS ONE · doi:10.1371/journal.pone.0171418 · Cited by 86

Astrocytic plasticity as a possible mediator of the cognitive improvements after environmental enrichment in aged rats

Sampedro‐Piquero, P., Bartolo, P. D., Petrosini, L., Zancada-Menéndez, C., Arias, J. L., & Begega, A. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.04.002 · Cited by 90

Aquaporin-4–dependent K+ and water transport modeled in brain extracellular space following neuroexcitation

Jin, B., Zhang, H., Binder, D. K., & Verkman, A. S. (2012) · The Journal of General Physiology · doi:10.1085/jgp.201210883 · Cited by 85

Role of glutamate receptors and glial cells in the pathophysiology of treatment-resistant depression

Kim, Y.-K., & Na, K.-S. (2016) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2016.03.009 · Cited by 84

The Brain Microenvironment and Cancer Metastasis

Fidler, I. J., Balasubramanian, K., Lin, Q., Kim, S. W., & Kim, S.-J. (2010) · Molecules and Cells · doi:10.1007/s10059-010-0133-9 · Cited by 84

Altered Waste Disposal System in Aging and Alzheimer’s Disease: Focus on Astrocytic Aquaporin-4

Valenza, M., Facchinetti, R., Steardo, L., & Scuderi, C. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01656 · Cited by 90

G-Protein Coupled Receptors and Tau-different Roles in Alzheimer’s Disease

Chidambaram, H., & Chinnathambi, S. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.04.019 · Cited by 87

Cell therapy centered on IL-1Ra is neuroprotective in experimental stroke

Clausen, B. H., Lambertsen, K. L., Dagnæs‐Hansen, F., Babcock, A. A., von Linstow, C. U., Meldgaard, M., Kristensen, B. W., Deierborg, T., & Finsen, B. R. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1541-5 · Cited by 82

Interleukin-17 (IL-17)-induced MicroRNA 873 (miR-873) Contributes to the Pathogenesis of Experimental Autoimmune Encephalomyelitis by Targeting A20 Ubiquitin-editing Enzyme

Liu, X., He, F., Pang, R., Zhao, D., Qiu, W., Shan, K., Zhang, J., Lu, Y., Li, Y., & Wang, Y. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.577429 · Cited by 85

Neural Mobilization Reverses Behavioral and Cellular Changes That Characterize Neuropathic Pain in Rats

dos Santos, F. M., Silva, J. T. D., Giardini, A. C., da Rocha, P. A. D. S., Achermann, A. P. P., Alves, A. S., Britto, L. R. G., & Chacur, M. (2012) · Molecular Pain · doi:10.1186/1744-8069-8-57 · Cited by 81

Neuronal scaling rules for primate brains

Herculano‐Houzel, S. (2012) · Progress in brain research · doi:10.1016/b978-0-444-53860-4.00015-5 · Cited by 82

Antioxidant and anti-senescence effect of metformin on mouse olfactory ensheathing cells (mOECs) may be associated with increased brain-derived neurotrophic factor levels-an ex vivo study

Śmieszek, A., Stręk, Z., Kornicka, K., Grzesiak, J., Weiss, C., & Marycz, K. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18040872 · Cited by 77

Glioblastoma’s Next Top Model: Novel Culture Systems for Brain Cancer Radiotherapy Research

Caragher, S. P., Chalmers, A. J., & Gomez-Roman, N. (2019) · Cancers · doi:10.3390/cancers11010044 · Cited by 80

Glial glucose fuels the neuronal pentose phosphate pathway for long-term memory

de Tredern, É., Rabah, Y., Pasquer, L., Minatchy, J., Plaçais, P.-Y., & Préat, T. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109620 · Cited by 79

High Purcell Factor Due To Coupling of a Single Emitter to a Dielectric Slot Waveguide

Kolchin, P., Pholchai, N., Mikkelsen, M. H., Oh, J., Ota, S., Islam, M. S., Yin, X., & Zhang, X. (2014) · Nano Letters · doi:10.1021/nl5037808 · Cited by 77

Characterization of AD-like phenotype in aged APPSwe/PS1dE9 mice

Huang, H., Nie, S., Cao, M., Marshall, C., Gao, J., Xiao, N., Hu, G., & Xiao, M. (2016) · AGE · doi:10.1007/s11357-016-9929-7 · Cited by 79

On the Concepts and History of Glioblastoma Multiforme - Morphology, Genetics and Epigenetics

Stoyanov, G. S., & Dzhenkov, D. L. (2018) · Folia Medica · doi:10.1515/folmed-2017-0069 · Cited by 77

Simple Precision Creation of Digitally Specified, Spatially Heterogeneous, Engineered Tissue Architectures

Gurkan, U. A., Fan, Y., Xu, F., Erkmen, B., Urkac, E. S., Parlakgül, G., Bernstein, J., Xing, W., Boyden, E. S., & Demirci, U. (2012) · Advanced Materials · doi:10.1002/adma.201203261 · Cited by 75

Loss of TDP-43 in astrocytes leads to motor deficits by triggering A1-like reactive phenotype and triglial dysfunction

Peng, A. Y. T., Agrawal, I., Ho, W. Y., Yen, Y.-C., Pinter, A. J., Liu, J., Phua, Q. X. C., Koh, K. B., Chang, J., Sanford, E., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2007806117 · Cited by 77

Metabolic compartmentalization between astroglia and neurons in physiological and pathophysiological conditions of the neurovascular unit

Takahashi, S. (2020) · Neuropathology · doi:10.1111/neup.12639 · Cited by 77

Intrathecal NGF Administration Reduces Reactive Astrocytosis and Changes Neurotrophin Receptors Expression Pattern in a Rat Model of Neuropathic Pain

Cirillo, G., Cavaliere, C., Bianco, M. R., Simone, A. D., Colangelo, A. M., Sellitti, S., Alberghina, L., & Papa, M. (2009) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-009-9430-2 · Cited by 75

Signaling pathways regulating neuron–glia interaction and their implications in Alzheimer's disease

Lian, H., & Zheng, H. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13424 · Cited by 77

PRNP/prion protein regulates the secretion of exosomes modulating CAV1/caveolin-1-suppressed autophagy

Dias, M. V. S., Teixeira, B. L., Rodrigues, B. R., Sinigaglia‐Coimbra, R., Porto-Carreiro, I., Roffé, M., Hajj, G. N. M., & Martins, V. R. (2016) · Autophagy · doi:10.1080/15548627.2016.1226735 · Cited by 79

Liposomal clodronate selectively eliminates microglia from primary astrocyte cultures

Kumamaru, H., Saiwai, H., Kobayakawa, K., Kubota, K., van Rooijen, N., Inoue, K., Iwamoto, Y., & Okada, S. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-116 · Cited by 76

Development of Neuroregenerative Gene Therapy to Reverse Glial Scar Tissue Back to Neuron-Enriched Tissue

Zhang, L., Lei, Z., Guo, Z., Pei, Z., Chen, Y., Zhang, F., Cai, A., Mok, G., Lee, G., Swaminathan, V., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.594170 · Cited by 88

Astrocytic ALKBH5 in stress response contributes to depressive-like behaviors in mice

Guo, F., Fan, J., Liu, J., Kong, P., Ren, J., Mo, J., Lu, C., Zhong, Q., Chen, L.-Y., Jiang, H.-T., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-48730-2 · Cited by 79

Distinct progenitor behavior underlying neocortical gliogenesis related to tumorigenesis

Shen, Z., Lin, Y., Yang, J., Jörg, D. J., Peng, Y., Zhang, X., Xu, Y., Hernandez, L., Ma, J., Simons, B. D., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108853 · Cited by 70

Astrocytes in neurodegenerative diseases (I): function and molecular description

Guillamón-Vivancos, T., Gómez‐Pinedo, U., & Matías‐Guiu, J. (2015) · Neurología (English Edition) · doi:10.1016/j.nrleng.2014.12.005 · Cited by 75

Astrocyte-derived growth factors and estrogen neuroprotection: Role of transforming growth factor-α in estrogen-induced upregulation of glutamate transporters in astrocytes

Karki, P., Smith, K., Johnson, J., & Lee, E. (2014) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2014.01.010 · Cited by 73

Degeneracy in hippocampal physiology and plasticity

Rathour, R. K., & Narayanan, R. (2019) · Hippocampus · doi:10.1002/hipo.23139 · Cited by 78

Connexin and pannexin signaling pathways, an architectural blueprint for CNS physiology and pathology?

Decrock, E., Bock, M. D., Wang, N., Bultynck, G., Giaume, C., Naus, C. C. G., Green, C. R., & Leybaert, L. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1962-7 · Cited by 78

Effects of lithium on lipopolysaccharide-induced inflammation in rat primary glia cells

Nahman, S., Belmaker, R., & Azab, A. N. (2011) · Innate Immunity · doi:10.1177/1753425911421512 · Cited by 73

A novel Drosophila injury model reveals severed axons are cleared through a Draper/MMP-1 signaling cascade

Purice, M. D., Ray, A., Muenzel, E. J., Pope, B. J., Park, D. J., Speese, S. D., & Logan, M. A. (2017) · eLife · doi:10.7554/elife.23611 · Cited by 75

MicroRNA‐365 modulates astrocyte conversion into neuron in adult rat brain after stroke by targeting Pax6

Mo, J., Liu, Q., Kou, Z., Wu, K., Yang, P., Chen, X., & Sun, F. (2018) · Glia · doi:10.1002/glia.23308 · Cited by 72

Long-term culture of astrocytes attenuates the readily releasable pool of synaptic vesicles

Kawano, H., Katsurabayashi, S., Kakazu, Y., Yamashita, Y., Kubo, N., Kubo, M., Okuda, H., Takasaki, K., Kubota, K., Mishima, K., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048034 · Cited by 68

Developmental Origins of Human Cortical Oligodendrocytes and Astrocytes

Yang, L., Li, Z., Liu, G., Li, X., & Yang, Z. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00759-9 · Cited by 75

The LIM Homeodomain Factor Lhx2 Is Required for Hypothalamic Tanycyte Specification and Differentiation

Salvatierra, J., Lee, D. A., Zibetti, C., Duran‐Moreno, M., Yoo, S., Newman, E. A., Wang, H., Bedont, J. L., de Melo, J., Miranda‐Angulo, A. L., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1711-14.2014 · Cited by 65

Astrocyte calcium signalling orchestrates neuronal synchronization in organotypic hippocampal slices

Sasaki, T., Ishikawa, T., Abe, R., Nakayama, R., Asada, A., Matsuki, N., & Ikegaya, Y. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.272864 · Cited by 74

Age-related changes in brain support cells: Implications for stroke severity

Sohrabji, F., Bake, S., & Lewis, D. K. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.06.013 · Cited by 74

The Emerging Role of the Interplay Among Astrocytes, Microglia, and Neurons in the Hippocampus in Health and Disease

Lana, D., Ugolini, F., Nosi, D., Wenk, G. L., & Giovannini, M. G. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.651973 · Cited by 73

Astrocytes as a target for therapeutic strategies in epilepsy: current insights

Çarçak, N., Onat, F., & Sitnikova, E. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1183775 · Cited by 70

Glial Fibrillary Tangles and JAK/STAT-Mediated Glial and Neuronal Cell Death in a Drosophila Model of Glial Tauopathy

Colodner, K. J., & Feany, M. Β. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2491-10.2010 · Cited by 71

Uptake and toxicity of copper oxide nanoparticles in cultured primary brain astrocytes

Bulcke, F., Thiel, K., & Dringen, R. (2013) · Nanotoxicology · doi:10.3109/17435390.2013.829591 · Cited by 68

Intracellular water preexchange lifetime in neurons and astrocytes

Yang, D. M., Huettner, J. E., Bretthorst, G. L., Neil, J. J., Garbow, J. R., & Ackerman, J. J. H. (2017) · Magnetic Resonance in Medicine · doi:10.1002/mrm.26781 · Cited by 68

The neuron-astrocyte-microglia triad involvement in neuroinflammaging mechanisms in the CA3 hippocampus of memory-impaired aged rats

Lana, D., Iovino, L., Nosi, D., Wenk, G. L., & Giovannini, M. G. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.07.011 · Cited by 68

Astrocytes to the rescue! Glia limitans astrocytic endfeet control CNS inflammation

Quintana, F. J. (2017) · Journal of Clinical Investigation · doi:10.1172/jci95769 · Cited by 66

Gut bacteria interaction with vagal afferents

Cawthon, C. R., & Serre, C. B. D. L. (2018) · Brain Research · doi:10.1016/j.brainres.2018.01.012 · Cited by 69

Myelin copper and the cuprizone model of schizophrenia

Konradi, C. L. (2010) · Frontiers in Bioscience-Scholar · doi:10.2741/s129 · Cited by 68

Differential Proliferation Rhythm of Neural Progenitor and Oligodendrocyte Precursor Cells in the Young Adult Hippocampus

Matsumoto, Y., Tsunekawa, Y., Nomura, T., Suto, F., Matsumata, M., Tsuchiya, S., & Osumi, N. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027628 · Cited by 66

Subregional differences in astrocytes underlie selective neurodegeneration or protection in Parkinson's disease models in culture

Kostuk, E. W., Cai, J., & Iacovitti, L. (2019) · Glia · doi:10.1002/glia.23627 · Cited by 67

Sonic hedgehog signaling in astrocytes

Hill, S. A., Fu, M., & Garcia, A. D. R. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03668-8 · Cited by 70

Structural reorganization of pyramidal neurons in the medial prefrontal cortex of alcohol dependent rats is associated with altered glial plasticity

Kim, A., Zamora-Martinez, E. R., Edwards, S., & Mandyam, C. D. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0755-3 · Cited by 64

A self-referencing glutamate biosensor for measuring real time neuronal glutamate flux

McLamore, E. S., Mohanty, S., Shi, J. P., Claussen, J. C., Jedlicka, S. S., Rickus, J. L., & Porterfield, D. M. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.03.001 · Cited by 64

Astrocytes in Migration

Zhan, J., Gao, K., Chai, R. C., Jia, X. H., Luo, D. P., Ge, G., Jiang, Y. W., Fung, Y. W., Li, L., & Yu, A. C. (2016) · Neurochemical Research · doi:10.1007/s11064-016-2089-4 · Cited by 73

The astrocyte biochemistry

de Souza, D. G., Almeida, R. F., Souza, D. O., & Zimmer, E. R. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.04.002 · Cited by 70

Astrocyte Form and Function in the Developing Central Nervous System

Chaboub, L. S., & Deneen, B. (2013) · Seminars in Pediatric Neurology · doi:10.1016/j.spen.2013.10.003 · Cited by 60

Developmental patterns of chimpanzee cerebral tissues provide important clues for understanding the remarkable enlargement of the human brain

Sakai, T., Matsui, M., Mikami, A., Málková, L., Hamada, Y., Tomonaga, M., Suzuki, J., Tanaka, M., Miyabe‐Nishiwaki, T., Makishima, H., et al. (2012) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2012.2398 · Cited by 61

AQP4 Knockout Aggravates Ischemia/Reperfusion Injury in Mice

Zeng, X., Xie, L., Liang, R., Sun, X., Fan, Y., & Hu, G. (2012) · CNS Neuroscience & Therapeutics · doi:10.1111/j.1755-5949.2012.00308.x · Cited by 62

IL-17A Induces MIP-1α Expression in Primary Astrocytes via Src/MAPK/PI3K/NF-kB Pathways: Implications for Multiple Sclerosis

Yi, H., Bai, Y., Zhu, X., Lin, L., Zhao, L., Wu, X., Buch, S. J., Wang, L., Chao, J., & Yao, H. (2014) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-014-9553-1 · Cited by 64

The Microbiota–Gut–Brain Axis and Alzheimer Disease. From Dysbiosis to Neurodegeneration: Focus on the Central Nervous System Glial Cells

Giovannini, M. G., Lana, D., Traini, C., & Vannucchi, M. G. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10112358 · Cited by 64

Stability of synchronization in simplicial complexes with multiple interaction layers

Anwar, M. S., & Ghosh, D. (2022) · Physical review. E · doi:10.1103/physreve.106.034314 · Cited by 61

Single-cell transcriptomic landscape of the developing human spinal cord

Andersen, J., Thom, N., Shadrach, J. L., Chen, X., Onesto, M. M., Amin, N. D., Yoon, S.-J., Li, L., Greenleaf, W. J., Müller, F., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01311-w · Cited by 61

Neurological manifestations of oculodentodigital dysplasia: a Cx43 channelopathy of the central nervous system?

Bock, M. D., Marianne, K., Wang, N., & Leybaert, L. (2013) · Frontiers in Pharmacology · doi:10.3389/fphar.2013.00120 · Cited by 62

The neuron-astrocyte-microglia triad in a rat model of chronic cerebral hypoperfusion: protective effect of dipyridamole

Lana, D., Melani, A., Pugliese, A. M., Cipriani, S., Nosi, D., Pedata, F., & Giovannini, M. G. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00322 · Cited by 63

Multiple Sclerosis is Not a Disease of the Immune System

Corthals, A. (2011) · The Quarterly Review of Biology · doi:10.1086/662453 · Cited by 61

Glia make up most of the cells in the brain, yet until recently they were believed to have only a passive, supporting role. It is now becoming increasingly clear that these cells have other functions: they make crucial contributions to the formation, operation and adaptation of neural circuitry.

Allen, N. J., & Barres, B. A. (2009)

New functions for glia in the brain

Temburni, M. K., & Jacob, M. H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081073198 · Cited by 57

Glee for Glia

Stern, P. (2010) · Science · doi:10.1126/science.330.6005.773 · Cited by 9

The Biology of GliaPreprint

Stevens, B., Monk, K. R., & Freeman, M. R. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041809

Introductory Speaker:

Diseases, G. (2013)