The homeostatic astroglia emerges from evolutionary specialization of neural cells
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Evolution of the nervous system progressed through cellular diversification and specialization of functions. Conceptually, the nervous system is composed from electrically excitable neuronal networks connected with chemical synapses and non-excitable glial cells that provide for homeostasis and defence. Astrocytes are integrated into neural networks through multipartite synapses; astroglial perisynaptic processes closely enwrap synaptic contacts and control homeostasis of the synaptic cleft, supply neurons with glutamate and GABA obligatory precursor glutamine and contribute to synaptic plasticity, learning and memory. In neuropathology, astrocytes may undergo reactive remodelling or degeneration; to a large extent, astroglial reactions define progression of the pathology and neurological outcome. This article is part of the themed issue ‘Evolution brings Ca 2+ and ATP together to control life and death’.
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Despite extensive studies in rodent models, the specific contributions of astrocytes to human pathology remain inadequately understood, partly due to species-specific differences.
“Despite extensive studies in rodent models, the specific contributions of astrocytes to human pathology remain inadequately understood, partly due to species-specific differences (17–20).”
From Varicose projection astrocytes: Conserved reactive cells in brain pathology (2026) · cites this paper as [19]
Section 3, “Singular human astrocytes” (page unavailable), describes substantial differences between human and rodent astrocytes. Section 7, “Neuropathology as a homeostatic failure” (page unavailable), discusses astrocyte contributions to disease and includes a rat experiment. The paper does not say that their contributions to human pathology remain inadequately understood because of species differences, or characterize the extent of rodent-model research. (LLM, conf=0.82)
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Iliff, J. J., Wang, M., Liao, Y., Plogg, B. A., Peng, W., Gundersen, G. A., Benveniste, H., Vates, G. E., Deane, R., Goldman, S. A., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003748 · Cited by 5,824 · see citing works
Self-citationSleep Drives Metabolite Clearance from the Adult Brain
Xie, L., Kang, H., Xu, Q., Chen, M. J., Liao, Y., Thiyagarajan, M., O’Donnell, J., Christensen, D. J., Nicholson, C., Iliff, J. J., et al. (2013) · Science · doi:10.1126/science.1241224 · Cited by 5,411 · see citing works
Self-citationThe glymphatic system: a beginner's guide
Jessen, N. A., Munk, A. S. F., Lundgaard, I., & Nedergaard, M. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1581-6 · Cited by 2,075 · see citing works
Self-citationAstrocyte-Neuron Lactate Transport Is Required for Long-Term Memory Formation
Suzuki, A., Stern, S. A., Bozdagi, O., Huntley, G. W., Walker, R. H., Magistretti, P. J., & Alberini, C. M. (2011) · Cell · doi:10.1016/j.cell.2011.02.018 · Cited by 1,711 · see citing works
Microglial interactions with synapses are modulated by visual experience
Tremblay, M.-È., Lowery, R. L., & Majewska, A. K. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000527 · Cited by 1,542 · see citing works
Kynurenines in the mammalian brain: when physiology meets pathology
Schwarcz, R., Bruno, J. P., Muchowski, P. J., & Wu, H.-Q. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3257 · Cited by 1,530 · see citing works
Impairment of paravascular clearance pathways in the aging brain
Kress, B. T., Iliff, J. J., Xia, M., Wang, M., Wei, H. S., Zeppenfeld, D., Xie, L., Kang, H., Xu, Q., Liew, J. A., et al. (2014) · Annals of Neurology · doi:10.1002/ana.24271 · Cited by 1,521 · see citing works
Self-citationAstrocytes mediate synapse elimination through MEGF10 and MERTK pathways
Chung, W.-S., Clarke, L. E., Wang, G. X., Stafford, B. K., Sher, A., Chakraborty, C., Joung, J., Foo, L. C., Thompson, A., Chen, C., et al. (2013) · Nature · doi:10.1038/nature12776 · Cited by 1,377 · see citing works
Microglia: new roles for the synaptic stripper
Kettenmann, H., Kirchhoff, F., & Verkhratsky, A. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.023 · Cited by 1,173 · see citing works
Self-citationAstrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis
Yamanaka, K., Chun, S. J., Boillee, S., Fujimori-Tonou, N., Yamashita, H., Gutmann, D. H., Takahashi, R., Misawa, H., & Cleveland, D. W. (2008) · Nature Neuroscience · doi:10.1038/nn2047 · Cited by 1,140 · see citing works
The tripartite synapse: roles for gliotransmission in health and disease
Halassa, M. M., Fellin, T., & Haydon, P. G. (2007) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2006.12.005 · Cited by 852 · see citing works
Regulation of synaptic connectivity by glia.
Eroglu, C., & Barres, B. A. (2010) · Nature · doi:10.1038/nature09612 · Cited by 813 · see citing works
Astrocytes as secretory cells of the central nervous system: idiosyncrasies of vesicular secretion
Verkhratsky, A., Matteoli, M., Parpura, V., Mothet, J., & Zorec, R. (2016) · The EMBO Journal · doi:10.15252/embj.201592705 · Cited by 397 · see citing works
Self-citationA quantitative study of the human cerebellum with unbiased stereological techniques
Andersen, B. B., Korbo, L., & Pakkenberg, B. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903260405 · Cited by 276 · see citing works
Astroglial cradle in the life of the synapse
Verkhratsky, A., & Nedergaard, M. (2014) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2013.0595 · Cited by 266 · see citing works
Self-citationMessing, A., Brenner, M., Feany, M. B., Nedergaard, M., & Goldman, J. E. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5384-11.2012 · Cited by 250 · see citing works
Self-citationEide, P. K., & Ringstad, G. (2015) · Acta Radiologica Open · doi:10.1177/2058460115609635 · Cited by 218 · see citing works
Glia:Neuron index: Review and hypothesis to account for different values in various mammals.
Reichenbach, A. (1989) · Glia · doi:10.1002/glia.440020202 · Cited by 97 · see citing works
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Research works printed but not linked: 142
- [1]Bartol TM, Bromer C, Kinney J, Chirillo MA, Bourne JN, Harris KM, Sejnowski TJ. 2015. Nanoconnectomic upper bound on the variability of synaptic plasticity. Elife 4, e10778 ( 10.7554/eLife.10778) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [2]Zhu XH, Qiao H, Du F, Xiong Q, Liu X, Zhang X, Ugurbil K, Chen W. 2012. Quantitative imaging of energy expenditure in human brain. Neuroimage 60, 2107–2117. ( 10.1016/j.neuroimage.2012.02.013) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [3]Magistretti PJ. 2009. Neuroscience. Low-cost travel in neurons. Science 325, 1349–1351. ( 10.1126/science.1180102) [DOI] [PubMed] [Google Scholar] · DOI
- [4]Molofsky AV, Deneen B. 2015. Astrocyte development: a guide for the perplexed. Glia 63, 1320–1329. ( 10.1002/glia.22836) [DOI] [PubMed] [Google Scholar] · DOI
- [5]Mitew S, Hay CM, Peckham H, Xiao J, Koenning M, Emery B. 2014. Mechanisms regulating the development of oligodendrocytes and central nervous system myelin. Neuroscience 276, 29–47. ( 10.1016/j.neuroscience.2013.11.029) [DOI] [PubMed] [Google Scholar] · DOI
- [6]Ginhoux F, Prinz M. 2015. Origin of microglia: current concepts and past controversies. Cold Spring Harb. Perspect. Biol. 7, a020537 ( 10.1101/cshperspect.a020537) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [7]Verkhratsky A, Butt AM. 2013. Glial physiology and pathophysiology, 560 p. Chichester, UK: Wiley-Blackwell. [Google Scholar]
- [8]Azevedo FA, Carvalho LR, Grinberg LT, Farfel JM, Ferretti RE, Leite RE, Jacob Filho W, Lent R, Herculano-Houzel S. 2009. Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain. J. Comp. Neurol. 513, 532–541. ( 10.1002/cne.21974) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [9]Hartline DK. 2011. The evolutionary origins of glia. Glia 59, 1215–1236. ( 10.1002/glia.21149) [DOI] [PubMed] [Google Scholar] · DOI
- [10]Oikonomou G, Shaham S. 2011. The glia of Caenorhabditis elegans. Glia 59, 1253–1263. ( 10.1002/glia.21084) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [11]Bacaj T, Tevlin M, Lu Y, Shaham S. 2008. Glia are essential for sensory organ function in C. elegans. Science 322, 744–747. ( 10.1126/science.1163074) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [12]Xu K, Terakawa S. 1999. Fenestration nodes and the wide submyelinic space form the basis for the unusually fast impulse conduction of shrimp myelinated axons. J. Exp. Biol. 202, 1979–1989. [DOI] [PubMed] [Google Scholar]
- [13]Edwards TN, Meinertzhagen IA. 2010. The functional organisation of glia in the adult brain of Drosophila and other insects. Prog. Neurobiol. 90, 471–497. ( 10.1016/j.pneurobio.2010.01.001) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [14]Hartenstein V. 2011. Morphological diversity and development of glia in Drosophila. Glia 59, 1237–1252. ( 10.1002/glia.21162) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [15]Parker RJ, Auld VJ. 2006. Roles of glia in the Drosophila nervous system. Semin. Cell Dev. Biol. 17, 66–77. ( 10.1016/j.semcdb.2005.11.012) [DOI] [PubMed] [Google Scholar] · DOI
- [16]Kettenmann H, Hanisch UK, Noda M, Verkhratsky A. 2011. Physiology of microglia. Physiol. Rev. 91, 461–553. ( 10.1152/physrev.00011.2010) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [17]Sild M, Ruthazer ES. 2011. Radial glia: progenitor, pathway, and partner. Neuroscientist 17, 288–302. ( 10.1177/1073858410385870) [DOI] [PubMed] [Google Scholar] · DOI
- [18]Mashanov VS, Zueva OR, Heinzeller T, Aschauer B, Naumann WW, Grondona JM, Cifuentes M, Garcia-Arraras JE. 2009. The central nervous system of sea cucumbers (Echinodermata: Holothuroidea) shows positive immunostaining for a chordate glial secretion. Front. Zool. 6, 11 ( 10.1186/1742-9994-6-11) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [19]Ari C, Kalman M. 2008. Glial architecture of the ghost shark (Callorhinchus milii, Holocephali, Chondrichthyes) as revealed by different immunohistochemical markers. J. Exp. Zool. B Mol. Dev. Evol. 310, 504–519. ( 10.1002/jez.b.21223) [DOI] [PubMed] [Google Scholar] · DOI
- [20]Ari C, Kalman M. 2008. Evolutionary changes of astroglia in Elasmobranchii comparing to amniotes: a study based on three immunohistochemical markers (GFAP, S-100, and glutamine synthetase). Brain Behav. Evol. 71, 305–324. ( 10.1159/000129654) [DOI] [PubMed] [Google Scholar] · DOI
- [21]Baumgart EV, Barbosa JS, Bally-Cuif L, Gotz M, Ninkovic J. 2010. Stab wound injury of the zebrafish telencephalon: a model for comparative analysis of reactive gliosis. Glia 60, 343–357. ( 10.1002/glia.22269) [DOI] [PubMed] [Google Scholar] · DOI
- [22]Reichenbach A, Neumann M, Bruckner G. 1987. Cell length to diameter relation of rat fetal radial glia—does impaired K+ transport capacity of long thin cells cause their perinatal transformation into multipolar astrocytes? Neurosci. Lett. 73, 95–100. ( 10.1016/0304-3940(87)90038-3) [DOI] [PubMed] [Google Scholar] · DOI
- [23]Kimelberg HK. 2010. Functions of mature mammalian astrocytes: a current view. Neuroscientist 16, 79–106. ( 10.1177/1073858409342593) [DOI] [PubMed] [Google Scholar] · DOI
- [25]Danbolt NC. 2001. Glutamate uptake. Prog. Neurobiol. 65, 1–105. ( 10.1016/S0301-0082(00)00067-8) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [26]Boison D, Chen JF, Fredholm BB. 2010. Adenosine signaling and function in glial cells. Cell Death Differ. 17, 1071–1082. ( 10.1038/cdd.2009.131) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [27]Deitmer JW, Rose CR. 1996. pH regulation and proton signalling by glial cells. Prog. Neurobiol. 48, 73–103. ( 10.1016/0301-0082(95)00039-9) [DOI] [PubMed] [Google Scholar] · DOI
- [28]Pellerin L, Magistretti PJ. 2012. Sweet sixteen for ANLS. J. Cereb. Blood Flow Metab. 32, 1152–1166. ( 10.1038/jcbfm.2011.149) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [30]Bushong EA, Martone ME, Jones YZ, Ellisman MH. 2002. Protoplasmic astrocytes in CA1 stratum radiatum occupy separate anatomical domains. J. Neurosci. 22, 183–192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [31]Nedergaard M, Ransom B, Goldman SA. 2003. New roles for astrocytes: redefining the functional architecture of the brain. Trends Neurosci. 26, 523–530. ( 10.1016/j.tins.2003.08.008) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [32]Emsley JG, Macklis JD. 2006. Astroglial heterogeneity closely reflects the neuronal-defined anatomy of the adult murine CNS. Neuron Glia Biol. 2, 175–186. ( 10.1017/S1740925X06000202) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [33]Matyash V, Kettenmann H. 2010. Heterogeneity in astrocyte morphology and physiology. Brain Res. Rev. 63, 2–10. ( 10.1016/j.brainresrev.2009.12.001) [DOI] [PubMed] [Google Scholar] · DOI
- [34]Matthias K, Kirchhoff F, Seifert G, Huttmann K, Matyash M, Kettenmann H, Steinhauser C. 2003. Segregated expression of AMPA-type glutamate receptors and glutamate transporters defines distinct astrocyte populations in the mouse hippocampus. J. Neurosci. 23, 1750–1758. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [35]Bayraktar OA, Fuentealba LC, Alvarez-Buylla A, Rowitch DH. 2015. Astrocyte development and heterogeneity. Cold Spring Harb. Perspect. Biol. 7, a020362 ( 10.1101/cshperspect.a020362) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [36]Garcia-Marques J, Lopez-Mascaraque L. 2013. Clonal identity determines astrocyte cortical heterogeneity. Cereb. Cortex 23, 1463–1472. ( 10.1093/cercor/bhs134) [DOI] [PubMed] [Google Scholar] · DOI
- [37]Oberheim NA, Goldman SA, Nedergaard M. 2012. Heterogeneity of astrocytic form and function. Methods Mol. Biol. 814, 23–45. ( 10.1007/978-1-61779-452-0_3) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [38]Verkhratsky A, Kettenmann H. 1996. Calcium signalling in glial cells. Trends Neurosci. 19, 346–352. ( 10.1016/0166-2236(96)10048-5) [DOI] [PubMed] [Google Scholar] · DOI
- [39]Verkhratsky A. 2010. Physiology of neuronal–glial networking. Neurochem. Int. 57, 332–343. ( 10.1016/j.neuint.2010.02.002) [DOI] [PubMed] [Google Scholar] · DOI
- [40]Kirchhoff F, Mulhardt C, Pastor A, Becker CM, Kettenmann H. 1996. Expression of glycine receptor subunits in glial cells of the rat spinal cord. J. Neurochem. 66, 1383–1390. ( 10.1046/j.1471-4159.1996.66041383.x) [DOI] [PubMed] [Google Scholar] · DOI
- [41]Kirischuk S, Kirchhoff F, Matyash V, Kettenmann H, Verkhratsky A. 1999. Glutamate-triggered calcium signalling in mouse Bergmann glial cells in situ: role of inositol-1,4,5-trisphosphate-mediated intracellular calcium release. Neuroscience 92, 1051–1059. ( 10.1016/S0306-4522(99)00067-6) [DOI] [PubMed] [Google Scholar] · DOI
- [42]Kirischuk S, Moller T, Voitenko N, Kettenmann H, Verkhratsky A. 1995. ATP-induced cytoplasmic calcium mobilization in Bergmann glial cells. J. Neurosci. 15, 7861–7871. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [43]Kirischuk S, Tuschick S, Verkhratsky A, Kettenmann H. 1996. Calcium signalling in mouse Bergmann glial cells mediated by α1-adrenoreceptors and H1 histamine receptors. Eur. J. Neurosci. 8, 1198–1208. ( 10.1111/j.1460-9568.1996.tb01288.x) [DOI] [PubMed] [Google Scholar] · DOI
- [44]Miyazaki I, Asanuma M, Diaz-Corrales FJ, Miyoshi K, Ogawa N. 2004. Direct evidence for expression of dopamine receptors in astrocytes from basal ganglia. Brain Res 1029, 120–123. ( 10.1016/j.brainres.2004.09.014) [DOI] [PubMed] [Google Scholar] · DOI
- [45]Verkhratsky A, Orkand RK, Kettenmann H. 1998. Glial calcium: homeostasis and signaling function. Physiol. Rev. 78, 99–141. [DOI] [PubMed] [Google Scholar]
- [46]Todd Farmer WT, et al. 2016. Neurons diversify astrocytes in the adult brain through sonic hedgehog signaling. Science 351, 849–854. ( 10.1126/science.aab3103) [DOI] [PubMed] [Google Scholar] · DOI
- [47]Verkhratsky A, Rodriguez JJ, Parpura V. 2012. Calcium signalling in astroglia. Mol. Cell Endocrinol. 353, 45–56. ( 10.1016/j.mce.2011.08.039) [DOI] [PubMed] [Google Scholar] · DOI
- [48]Rusakov DA. 2015. Disentangling calcium-driven astrocyte physiology. Nat. Rev. Neurosci. 16, 226–233. ( 10.1038/nrn3878) [DOI] [PubMed] [Google Scholar] · DOI
- [49]Rose CR, Verkhratsky A. 2016. Principles of sodium homeostasis and sodium signalling in astroglia. Glia, E-pub ahead of print. ( 10.1002/glia.22964) [DOI] [PubMed] [Google Scholar] · DOI
- [50]Kirischuk S, Parpura V, Verkhratsky A. 2012. Sodium dynamics: another key to astroglial excitability? Trends Neurosci. 35, 497–506. ( 10.1016/j.tins.2012.04.003) [DOI] [PubMed] [Google Scholar] · DOI
- [51]Parpura V, Verkhratsky A. 2012. Homeostatic function of astrocytes: Ca2+ and Na+ signalling. Transl. Neurosci. 3, 334–344. ( 10.2478/s13380-012-0040-y) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [52]Verkhratsky A, Kirchhoff F. 2007. NMDA receptors in glia. Neuroscientist 13, 28–37. ( 10.1177/1073858406294270) [DOI] [PubMed] [Google Scholar] · DOI
- [53]Verkhratsky A, Krishtal OA, Burnstock G. 2009. Purinoceptors on neuroglia. Mol. Neurobiol. 39, 190–208. ( 10.1007/s12035-009-8063-2) [DOI] [PubMed] [Google Scholar] · DOI
- [54]Verkhratsky A, Reyes RC, Parpura V. 2014. TRP channels coordinate ion signalling in astroglia. Rev. Physiol. Biochem. Pharmacol. 166, 1–22. ( 10.1007/112_2013_15) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [55]Araque A, Parpura V, Sanzgiri RP, Haydon PG. 1999. Tripartite synapses: glia, the unacknowledged partner. Trends Neurosci. 22, 208–215. ( 10.1016/S0166-2236(98)01349-6) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [58]Mayford M, Siegelbaum SA, Kandel ER. 2012. Synapses and memory storage. Cold Spring Harb. Perspect. Biol. 4, a005751 ( 10.1101/cshperspect.a005751) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [61]Dityatev A, Rusakov DA. 2011. Molecular signals of plasticity at the tetrapartite synapse. Curr. Opin. Neurobiol. 21, 353–359. ( 10.1016/j.conb.2010.12.006) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [62]Pfrieger FW. 2002. Role of glia in synapse development. Curr. Opin. Neurobiol. 12, 486–490. ( 10.1016/S0959-4388(02)00358-6) [DOI] [PubMed] [Google Scholar] · DOI
- [64]Nedergaard M, Verkhratsky A. 2012. Artifact versus reality—how astrocytes contribute to synaptic events. Glia 60, 1013–1023. ( 10.1002/glia.22288) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [65]Grosche J, Matyash V, Moller T, Verkhratsky A, Reichenbach A, Kettenmann H. 1999. Microdomains for neuron–glia interaction: parallel fiber signaling to Bergmann glial cells. Nat. Neurosci. 2, 139–143. ( 10.1038/5692) [DOI] [PubMed] [Google Scholar] · DOI
- [66]Reichenbach A, Derouiche A, Kirchhoff F. 2010. Morphology and dynamics of perisynaptic glia. Brain Res. Rev. 63, 11–25. ( 10.1016/j.brainresrev.2010.02.003) [DOI] [PubMed] [Google Scholar] · DOI
- [67]Peters A, Palay SL, Webster HF. 1991. The fine structure of the nervous system: the neurons and supporting cells, 3rd edn New York, NY: Oxford University Press. [Google Scholar]
- [68]Derouiche A. 2003. The perisynaptic astrocyte process as a glial compartment-immunolabeling for glutamine synthetase and other glial markers. Adv. Mol. Cell Biol. 31, 147–163. ( 10.1016/S1569-2558(03)31006-9) [DOI] [Google Scholar] · DOI
- [69]Derouiche A, Haseleu J, Korf HW. 2015. Fine astrocyte processes contain very small mitochondria: glial oxidative capability may fuel transmitter metabolism. Neurochem. Res. 40, 2402–2413. ( 10.1007/s11064-015-1563-8) [DOI] [PubMed] [Google Scholar] · DOI
- [70]Lavialle M, Aumann G, Anlauf E, Prols F, Arpin M, Derouiche A. 2011. Structural plasticity of perisynaptic astrocyte processes involves ezrin and metabotropic glutamate receptors. Proc. Natl Acad. Sci. USA 108, 12915–12919. ( 10.1073/pnas.1100957108) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [71]Derouiche A, Frotscher M. 2001. Peripheral astrocyte processes: monitoring by selective immunostaining for the actin-binding ERM proteins. Glia 36, 330–341. ( 10.1002/glia.1120) [DOI] [PubMed] [Google Scholar] · DOI
- [72]Hirrlinger J, Hulsmann S, Kirchhoff F. 2004. Astroglial processes show spontaneous motility at active synaptic terminals in situ. Eur. J. Neurosci. 20, 2235–2239. ( 10.1111/j.1460-9568.2004.03689.x) [DOI] [PubMed] [Google Scholar] · DOI
- [73]Heller JP, Rusakov DA. 2015. Morphological plasticity of astroglia: understanding synaptic microenvironment. Glia 63, 2133–2151. ( 10.1002/glia.22821) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [74]Oberheim NA, Wang X, Goldman S, Nedergaard M. 2006. Astrocytic complexity distinguishes the human brain. Trends Neurosci. 29, 547–553. ( 10.1016/j.tins.2006.08.004) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [75]Pentreath VW, Radojcic T, Seal LH, Winstanley EK. 1985. The glial cells and glia–neuron relations in the buccal ganglia of Planorbis corneus (L.): cytological, qualitative and quantitative changes during growth and ageing. Phil. Trans. R. Soc. Lond. B 307, 399–455. ( 10.1098/rstb.1985.0002) [DOI] [PubMed] [Google Scholar] · DOI
- [76]Herculano-Houzel S, Lent R. 2005. Isotropic fractionator: a simple, rapid method for the quantification of total cell and neuron numbers in the brain. J. Neurosci. 25, 2518–2521. ( 10.1523/JNEUROSCI.4526-04.2005) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [77]Lent R, Azevedo FA, Andrade-Moraes CH, Pinto AV. 2012. How many neurons do you have? Some dogmas of quantitative neuroscience under revision. Eur. J. Neurosci. 35, 1–9. ( 10.1111/j.1460-9568.2011.07923.x) [DOI] [PubMed] [Google Scholar] · DOI
- [78]Pakkenberg H. 1966. The number of nerve cells in the cerebral cortex of man. J. Comp. Neurol. 128, 17–20. ( 10.1002/cne.901280103) [DOI] [PubMed] [Google Scholar] · DOI
- [79]Pelvig DP, Pakkenberg H, Stark AK, Pakkenberg B. 2008. Neocortical glial cell numbers in human brains. Neurobiol. Aging 29, 1754–1762. ( 10.1016/j.neurobiolaging.2007.04.013) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [82]Chan-Palay V, Palay SL. 1972. The form of velate astrocytes in the cerebellar cortex of monkey and rat: high voltage electron microscopy of rapid Golgi preparations. Z. Anat. Entwicklungsgesch 138, 1–19. ( 10.1007/BF00519921) [DOI] [PubMed] [Google Scholar] · DOI
- [83]Hoogland TM, Kuhn B. 2010. Recent developments in the understanding of astrocyte function in the cerebellum in vivo. Cerebellum 9, 264–271. ( 10.1007/s12311-009-0139-z) [DOI] [PubMed] [Google Scholar] · DOI
- [84]Sherwood CC, et al. 2006. Evolution of increased glia–neuron ratios in the human frontal cortex. Proc. Natl Acad. Sci. USA 103, 13 606–13 611. ( 10.1073/pnas.0605843103) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [85]Oberheim NA, et al. 2009. Uniquely hominid features of adult human astrocytes. J. Neurosci. 29, 3276–3287. ( 10.1523/JNEUROSCI.4707-08.2009) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [86]Colombo JA, Reisin HD. 2004. Interlaminar astroglia of the cerebral cortex: a marker of the primate brain. Brain Res. 1006, 126–131. ( 10.1016/j.brainres.2004.02.003) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [87]Colombo JA, Sherwood CC, Hof PR. 2004. Interlaminar astroglial processes in the cerebral cortex of great apes. Anat. Embryol. (Berl.) 208, 215–218. ( 10.1007/s00429-004-0391-4) [DOI] [PubMed] [Google Scholar] · DOI
- [88]Colombo JA, Yanez A, Puissant V, Lipina S. 1995. Long, interlaminar astroglial cell processes in the cortex of adult monkeys. J. Neurosci. Res. 40, 551–556. ( 10.1002/jnr.490400414) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [89]Han X, et al. 2013. Forebrain engraftment by human glial progenitor cells enhances synaptic plasticity and learning in adult mice. Cell Stem Cell 12, 342–353. ( 10.1016/j.stem.2012.12.015) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [90]Windrem MS, Schanz SJ, Morrow C, Munir J, Chandler-Militello D, Wang S, Goldman SA. 2014. A competitive advantage by neonatally engrafted human glial progenitors yields mice whose brains are chimeric for human glia. J. Neurosci. 34, 16 153–16 161. ( 10.1523/JNEUROSCI.1510-14.2014) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [91]Waagepetersen HS, Qu H, Schousboe A, Sonnewald U. 2001. Elucidation of the quantitative significance of pyruvate carboxylation in cultured cerebellar neurons and astrocytes. J. Neurosci. Res. 66, 763–770. ( 10.1002/jnr.10061) [DOI] [PubMed] [Google Scholar] · DOI
- [92]Cesar M, Hamprecht B. 1995. Immunocytochemical examination of neural rat and mouse primary cultures using monoclonal antibodies raised against pyruvate carboxylase. J. Neurochem. 64, 2312–2318. ( 10.1046/j.1471-4159.1995.64052312.x) [DOI] [PubMed] [Google Scholar] · DOI
- [93]Martinez-Hernandez A, Bell KP, Norenberg MD. 1977. Glutamine synthetase: glial localization in brain. Science 195, 1356–1358. ( 10.1126/science.14400) [DOI] [PubMed] [Google Scholar] · DOI
- [94]Norenberg MD, Martinez-Hernandez A. 1979. Fine structural localization of glutamine synthetase in astrocytes of rat brain. Brain Res. 161, 303–310. ( 10.1016/0006-8993(79)90071-4) [DOI] [PubMed] [Google Scholar] · DOI
- [95]Conti F, DeBiasi S, Minelli A, Rothstein JD, Melone M. 1998. EAAC1, a high-affinity glutamate tranporter, is localized to astrocytes and gabaergic neurons besides pyramidal cells in the rat cerebral cortex. Cereb. Cortex 8, 108–116. ( 10.1093/cercor/8.2.108) [DOI] [PubMed] [Google Scholar] · DOI
- [96]Mackenzie B, Erickson JD. 2004. Sodium-coupled neutral amino acid (System N/A) transporters of the SLC38 gene family. Pflugers Arch. 447, 784–795. ( 10.1007/s00424-003-1117-9). [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [97]Rusakov DA. 2012. Astroglial glutamate transporters trigger glutaminergic gliotransmission. J. Physiol. 590, 2187–2188. ( 10.1113/jphysiol.2012.233577) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [98]Uwechue NM, Marx MC, Chevy Q, Billups B. 2012. Activation of glutamate transport evokes rapid glutamine release from perisynaptic astrocytes. J. Physiol. 590, 2317–2331. ( 10.1113/jphysiol.2011.226605) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [99]Martinez-Lozada Z et al. 2013. GLAST/EAAT1-induced glutamine release via SNAT3 in Bergmann glial cells: evidence of a functional and physical coupling. J. Neurochem. 125, 545–554. ( 10.1111/jnc.12211) [DOI] [PubMed] [Google Scholar] · DOI
- [100]Billups D, Marx MC, Mela I, Billups B. 2013. Inducible presynaptic glutamine transport supports glutamatergic transmission at the calyx of Held synapse. J. Neurosci. 33, 17 429–17 434. ( 10.1523/JNEUROSCI.1466-13.2013) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [101]Tani H, Dulla CG, Farzampour Z, Taylor-Weiner A, Huguenard JR, Reimer RJ. 2014. A local glutamate–glutamine cycle sustains synaptic excitatory transmitter release. Neuron 81, 888–900. ( 10.1016/j.neuron.2013.12.026) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [102]Unichenko P, Myakhar O, Kirischuk S. 2012. Intracellular Na+ concentration influences short-term plasticity of glutamate transporter-mediated currents in neocortical astrocytes. Glia 60, 605–614. ( 10.1002/glia.22294) [DOI] [PubMed] [Google Scholar] · DOI
- [103]Eulenburg V, Gomeza J. 2010. Neurotransmitter transporters expressed in glial cells as regulators of synapse function. Brain Res. Rev. 63, 103–112. ( 10.1016/j.brainresrev.2010.01.003) [DOI] [PubMed] [Google Scholar] · DOI
- [104]Peng L, Huang R, Yu AC, Fung KY, Rathbone MP, Hertz L. 2005. Nucleoside transporter expression and function in cultured mouse astrocytes. Glia 52, 25–35. ( 10.1002/glia.20216) [DOI] [PubMed] [Google Scholar] · DOI
- [105]Hertz L. 1965. Possible role of neuroglia: a potassium-mediated neuronal–neuroglial–neuronal impulse transmission system. Nature 206, 1091–1094. ( 10.1038/2061091a0) [DOI] [PubMed] [Google Scholar] · DOI
- [106]Macaulay N, Zeuthen T. 2012. Glial K+ clearance and cell swelling: key roles for cotransporters and pumps. Neurochem. Res. 37, 2299–2309. ( 10.1007/s11064-012-0731-3) [DOI] [PubMed] [Google Scholar] · DOI
- [107]Olsen ML, Sontheimer H. 2008. Functional implications for Kir4.1 channels in glial biology: from K+ buffering to cell differentiation. J. Neurochem. 107, 589–601. ( 10.1111/j.1471-4159.2008.05615.x) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [108]Kofuji P, Newman EA. 2004. Potassium buffering in the central nervous system. Neuroscience 129, 1045–1056. ( 10.1016/j.neuroscience.2004.06.008) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [109]Deitmer JW, Rose CR. 2010. Ion changes and signalling in perisynaptic glia. Brain Res. Rev. 63, 113–129. ( 10.1016/j.brainresrev.2009.10.006) [DOI] [PubMed] [Google Scholar] · DOI
- [110]Zanotti S, Charles A. 1997. Extracellular calcium sensing by glial cells: low extracellular calcium induces intracellular calcium release and intercellular signaling. J. Neurochem. 69, 594–602. ( 10.1046/j.1471-4159.1997.69020594.x) [DOI] [PubMed] [Google Scholar] · DOI
- [111]Segawa S, Nishiura T, Furuta T, Ohsato Y, Tani M, Nishida K, Nagasawa K. 2014. Zinc is released by cultured astrocytes as a gliotransmitter under hypoosmotic stress-loaded conditions and regulates microglial activity. Life Sci. 94, 137–144. ( 10.1016/j.lfs.2013.11.007) [DOI] [PubMed] [Google Scholar] · DOI
- [112]Ding F, O'Donnell J, Xu Q, Kang N, Goldman N, Nedergaard M. 2016. Changes in the composition of brain interstitial ions control the sleep–wake cycle. Science 352, 550–555. ( 10.1126/science.aad4821) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [113]Iliff JJ, Lee H, Yu M, Feng T, Logan J, Nedergaard M, Benveniste H. 2013. Brain-wide pathway for waste clearance captured by contrast-enhanced MRI. J. Clin. Invest. 123, 1299–1309. ( 10.1172/JCI67677) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [115]Mathiisen TM, Lehre KP, Danbolt NC, Ottersen OP. 2010. The perivascular astroglial sheath provides a complete covering of the brain microvessels: an electron microscopic 3D reconstruction. Glia 58, 1094–1103. ( 10.1002/glia.20990) [DOI] [PubMed] [Google Scholar] · DOI
- [117]Iliff JJ, Goldman SA, Nedergaard M. 2015. Implications of the discovery of brain lymphatic pathways. Lancet Neurol. 14, 977–979. ( 10.1016/S1474-4422(15)00221-5) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [121]Kiviniemi V, et al. 2015. Ultra-fast magnetic resonance encephalography of physiological brain activity—glymphatic pulsation mechanisms? J. Cereb. Blood Flow Metab. E-pub ahead of print. ( 10.1177/0271678X15622047) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [122]Cajal S. 1894. The Croonian lecture: la fine structure des centres nerveux. Proc. R. Soc. Lond. 55, 444–468. ( 10.1098/rspl.1894.0063) [DOI] [Google Scholar] · DOI
- [123]Kandel ER, Dudai Y, Mayford MR. 2014. The molecular and systems biology of memory. Cell 157, 163–186. ( 10.1016/j.cell.2014.03.001) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [124]Zorec R, Horvat A, Vardjan N, Verkhratsky A. 2015. Memory formation shaped by astroglia. Front. Integr. Neurosci. 9, 56 ( 10.3389/fnint.2015.00056) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [125]Ostroff LE, Manzur MK, Cain CK, Ledoux JE. 2014. Synapses lacking astrocyte appear in the amygdala during consolidation of Pavlovian threat conditioning. J. Comp. Neurol. 522, 2152–2163. ( 10.1002/cne.23523) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [126]Oliet SH, Piet R. 2004. Anatomical remodelling of the supraoptic nucleus: changes in synaptic and extrasynaptic transmission. J. Neuroendocrinol. 16, 303–307. ( 10.1111/j.0953-8194.2004.01159.x) [DOI] [PubMed] [Google Scholar] · DOI
- [127]Theodosis DT, Poulain DA, Oliet SH. 2008. Activity-dependent structural and functional plasticity of astrocyte–neuron interactions. Physiol. Rev. 88, 983–1008. ( 10.1152/physrev.00036.2007) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [128]Gibbs ME, Anderson DG, Hertz L. 2006. Inhibition of glycogenolysis in astrocytes interrupts memory consolidation in young chickens. Glia 54, 214–222. ( 10.1002/glia.20377) [DOI] [PubMed] [Google Scholar] · DOI
- [129]Hertz L, Gibbs ME. 2009. What learning in day-old chickens can teach a neurochemist: focus on astrocyte metabolism. J. Neurochem. 109(Suppl 1), 10–16. ( 10.1111/j.1471-4159.2009.05939.x) [DOI] [PubMed] [Google Scholar] · DOI
- [131]Ding F, O'Donnell J, Thrane AS, Zeppenfeld D, Kang H, Xie L, Wang F, Nedergaard M. 2013. α1-adrenergic receptors mediate coordinated Ca2+ signaling of cortical astrocytes in awake, behaving mice. Cell Calcium 54, 387–394. ( 10.1016/j.ceca.2013.09.001) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [132]Shain W, Forman DS, Madelian V, Turner JN. 1987. Morphology of astroglial cells is controlled by beta-adrenergic receptors. J. Cell Biol. 105, 2307–2314. ( 10.1083/jcb.105.5.2307) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [133]Shao Y, Enkvist MO, McCarthy KD. 1994. Glutamate blocks astroglial stellation: effect of glutamate uptake and volume changes. Glia 11, 1–10. ( 10.1002/glia.440110103) [DOI] [PubMed] [Google Scholar] · DOI
- [134]Won CL, Oh YS. 2000. cAMP-induced stellation in primary astrocyte cultures with regional heterogeneity. Brain Res. 887, 250–258. ( 10.1016/S0006-8993(00)02922-X) [DOI] [PubMed] [Google Scholar] · DOI
- [135]Vardjan N, Kreft M, Zorec R. 2014. Dynamics of beta-adrenergic/cAMP signaling and morphological changes in cultured astrocytes. Glia 62, 566–579. ( 10.1002/glia.22626) [DOI] [PubMed] [Google Scholar] · DOI
- [136]Burda JE, Sofroniew MV. 2014. Reactive gliosis and the multicellular response to CNS damage and disease. Neuron 81, 229–248. ( 10.1016/j.neuron.2013.12.034) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [137]Nedergaard M, Rodriguez JJ, Verkhratsky A. 2010. Glial calcium and diseases of the nervous system. Cell Calcium 47, 140–149. ( 10.1016/j.ceca.2009.11.010) [DOI] [PubMed] [Google Scholar] · DOI
- [138]Rajkowska G, Stockmeier CA. 2013. Astrocyte pathology in major depressive disorder: insights from human postmortem brain tissue. Curr. Drug Targets 14, 1225–1236. ( 10.2174/13894501113149990156) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [139]Verkhratsky A, Marutle A, Rodriguez-Arellano JJ, Nordberg A. 2014. Glial asthenia and functional paralysis: a new perspective on neurodegeneration and Alzheimer's disease. Neuroscientist 21, 552–568. ( 10.1177/1073858414547132) [DOI] [PubMed] [Google Scholar] · DOI
- [140]Verkhratsky A, Rodriguez JJ, Steardo L. 2014. Astrogliopathology: a central element of neuropsychiatric diseases? Neuroscientist 20, 576–588. ( 10.1177/1073858413510208) [DOI] [PubMed] [Google Scholar] · DOI
- [141]Verkhratsky A, Sofroniew MV, Messing A, deLanerolle NC, Rempe D, Rodriguez JJ, Nedergaard M. 2012. Neurological diseases as primary gliopathies: a reassessment of neurocentrism. ASN Neuro 4, e0082 ( 10.1042/AN20120010) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [142]Pekny M, Pekna M, Messing A, Steinhauser C, Lee JM, Parpura V, Hol EM, Sofroniew MV, Verkhratsky A. 2016. Astrocytes: a central element in neurological diseases. Acta Neuropathol. 131, 323–345. ( 10.1007/s00401-015-1513-1) [DOI] [PubMed] [Google Scholar] · DOI
- [143]Banasr M, Duman RS. 2008. Glial loss in the prefrontal cortex is sufficient to induce depressive-like behaviors. Biol. Psychiatry 64, 863–870. ( 10.1016/j.biopsych.2008.06.008) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [144]Bowley MP, Drevets WC, Ongur D, Price JL. 2002. Low glial numbers in the amygdala in major depressive disorder. Biol. Psychiatry 52, 404–412. ( 10.1016/S0006-3223(02)01404-X) [DOI] [PubMed] [Google Scholar] · DOI
- [145]Cotter D, Mackay D, Chana G, Beasley C, Landau S, Everall IP. 2002. Reduced neuronal size and glial cell density in area 9 of the dorsolateral prefrontal cortex in subjects with major depressive disorder. Cereb. Cortex 12, 386–394. ( 10.1093/cercor/12.4.386) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [146]Falkai P, Bogerts B. 1986. Cell loss in the hippocampus of schizophrenics. Eur. Arch. Psychiatry Neurol. Sci. 236, 154–161. ( 10.1007/BF00380943) [DOI] [PubMed] [Google Scholar] · DOI
- [147]Choudary PV, et al. 2005. Altered cortical glutamatergic and GABAergic signal transmission with glial involvement in depression. Proc. Natl Acad. Sci. USA 102, 15 653–15 658. ( 10.1073/pnas.0507901102) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [148]Sanacora G, Treccani G, Popoli M. 2012. Towards a glutamate hypothesis of depression: an emerging frontier of neuropsychopharmacology for mood disorders. Neuropharmacology 62, 63–77. ( 10.1016/j.neuropharm.2011.07.036) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [150]Schwarcz R, Hunter CA. 2007. Toxoplasma gondii and schizophrenia: linkage through astrocyte-derived kynurenic acid? Schizophr. Bull. 33, 652–653. ( 10.1093/schbul/sbm030) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [151]Hazell AS. 2009. Astrocytes are a major target in thiamine deficiency and Wernicke's encephalopathy. Neurochem. Int. 55, 129–135. ( 10.1016/j.neuint.2009.02.020) [DOI] [PubMed] [Google Scholar] · DOI
- [152]Hazell AS, Sheedy D, Oanea R, Aghourian M, Sun S, Jung JY, Wang D, Wang C. 2009. Loss of astrocytic glutamate transporters in Wernicke encephalopathy. Glia 58, 148–156. ( 10.1002/glia.20908) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [153]Czeh B, Di Benedetto B. 2013. Antidepressants act directly on astrocytes: evidences and functional consequences. Eur. Neuropsychopharmacol. 23, 171–185. ( 10.1016/j.euroneuro.2012.04.017) [DOI] [PubMed] [Google Scholar] · DOI
- [154]Peng L, Verkhratsky A, Gu L, Li B. 2015. Targeting astrocytes in major depression. Expert Rev. Neurother. 15, 1299–1306. ( 10.1586/14737175.2015.1095094) [DOI] [PubMed] [Google Scholar] · DOI
- [156]Montana V, Verkhratsky A, Parpura V. 2014. Pathological role for exocytotic glutamate release from astrocytes in hepatic encephalopathy. Curr. Neuropharmacol. 12, 324–333. ( 10.2174/1570159X12666140903094700) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- [157]Bedner P, et al. 2015. Astrocyte uncoupling as a cause of human temporal lobe epilepsy. Brain 138, 1208–1222. ( 10.1093/brain/awv067) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [158]Papadeas ST, Kraig SE, O'Banion C, Lepore AC, Maragakis NJ. 2011. Astrocytes carrying the superoxide dismutase 1 (SOD1G93A) mutation induce wild-type motor neuron degeneration in vivo. Proc. Natl Acad. Sci. USA 108, 17 803–17 808. ( 10.1073/pnas.1103141108) [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [159]Rossi D, Brambilla L, Valori CF, Roncoroni C, Crugnola A, Yokota T, Bredesen DE, Volterra A. 2008. Focal degeneration of astrocytes in amyotrophic lateral sclerosis. Cell Death Differ. 15, 1691–1700. ( 10.1038/cdd.2008.99) [DOI] [PubMed] [Google Scholar] · DOI · Paper page
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Self-citation
- Authors
- Verkhratsky, A., & Nedergaard, M.
- Affiliations
- Ikerbasque (ES)
- University of Copenhagen (DK)
- Corresponding author
- Verkhratsky, Alexei
- Nedergaard, Maiken
- Venue
- Philosophical Transactions of the Royal Society B: Biological Sciences
- Publisher
- The Royal Society
- Published
- 2016-08-05
- Volume
- 371
- Issue
- 1700
- Pages
- 20150428
- ISSN
- 0962-8436 (ISSN-L)
- 1471-2970
- PMC
- PMC4938028
- OpenAlex
- W2469873988
- Cited by
- 133
- References
- 18
- Citations by year
- 2026: 5 · 2025: 22 · 2024: 11 · 2023: 13 · 2022: 9 · 2021: 15 · 2020: 15 · 2019: 18 · 2018: 10 · 2017: 11 · 2016: 4
- FWCI
- 1.57
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Philosophical Transactions of the Royal Society B Biological Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (publishedVersion, other-oa)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Funders
- Wellcome Trust
- Ministry of Education and Science of Russia (contract 14.581.21.00.16, Project ID RFMEFI158115X0016)
- Joint Programme-Neurodegenerative Disease Research (JPND) project funded by the European Union's Horizon 2020 research and innovation programme (No. 643417, (DACAPO-AD))
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- astrocytes, nervous system evolution, glial cells, synaptic homeostasis, glutamine, synaptic plasticity, reactive astrogliosis, astrocyte degeneration
- MeSH terms
- Astrocytes, Biological Evolution, Homeostasis, Neurons, Synapses
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