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Shusharina N.N.

Immanuel Kant Baltic Federal University, Kaliningrad, Russia

Patrushev M.V.

Immanuel Kant Baltic Federal University, Kaliningrad, Russia

Silina E.V.

Kafedra patofiziologii FPPO vracheĭ Moskovskoĭ meditsinskoĭ akademii im. I.M. Sechenova

Stupin V.A.

GBOU VPO Rossiĭskiĭ natsional'nyĭ issledovatel'skiĭ meditsinskiĭ universitet im. N.I. Pirogova, kafedra gospital'noĭ khirurgii #1

Litvitsky P.F.

Chair of Hospital-Based Therapy №2, Chair of Pathophysiology of Medical Faculty, Sechenov First Moscow State Medical University of Ministry of Health of Russia, Moscow, Russia

Orlova A.S.

I.M. Sechenov First Moscow State Medical University, Moscow

Expression of genes for neurotransmitter transporters in astrocytes in different brain regions in experiment

Authors:

Shusharina N.N., Patrushev M.V., Silina E.V., Stupin V.A., Litvitsky P.F., Orlova A.S.

More about the authors

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To cite this article:

Shusharina NN, Patrushev MV, Silina EV, Stupin VA, Litvitsky PF, Orlova AS. Expression of genes for neurotransmitter transporters in astrocytes in different brain regions in experiment. S.S. Korsakov Journal of Neurology and Psychiatry. 2018;118(6):58‑64. (In Russ.)
https://doi.org/10.17116/jnevro20181186158

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References:

  1. Erkkinen MG, Kim MO, Geschwind MD. Clinical Neurology and Epidemiology of the Major Neurodegenerative Diseases. Cold Spring Harb Perspect Biol. 2017;033118. https://doi.org/10.1101/cshperspect.a033118
  2. Xu T, Clemson L, O’Loughlin K, Lannin NA, Dean C, Koh G. Risk factors for falls in community stroke survivors: A systematic review and meta-analysis. Arch Phys Med Rehabil. 2017. https://doi.org/10.1016/j.apmr.2017.06.032
  3. Ritchie CW, Molinuevo JL, Truyen L, Satlin A, Van der Geyten S, Lovestone S. Development of interventions for the secondary prevention of Alzheimer’s dementia: the European Prevention of Alzheimer’s Dementia (EPAD) project. Lancet Psychiatry. 2016;3:179-186. https://doi.org/10.1016/s2215-0366(15)00454-x
  4. Pringsheim T, Jette N, Frolkis A, Steeves TD. The prevalence of Parkinson’s disease: a systematic review and meta-analysis. Mov Disord. 2014;29(13):1583-1590. https://doi.org/10.1002/mds.25945
  5. Rumyantseva SA, Silina EV, Svischeva SP, Komarov AN. Medical and organizational issues of pre- and post-stroke disablement. Zhurnal Nevrologii i Psihiatrii im S.S. Korsakova. 2013;113:9:43-49 (In Russ.)
  6. Kamchatnov PR, Chugunov AV. Khronicheskie tserebrovaskulyarnye zabolevaniya. Doktor.Ru. 2017;1(130): 11-15. (In Russ.)
  7. Verkhratsky A. Sofroniew M, Messing A, deLanerolle NC, Rempe D, Rodríguez JJ, Nedergaard M. Neurological diseases as primary gliopathies: a reassessment of neurocentrism. ASN Neuro. 2012;4:00082. https://doi.org/10.1042/an20120010
  8. Eulenburg V, Gomeza J. Neurotransmitter transporters expressed in glial cells as regulators of synapse function. Brain research reviews. 2010;63(1):103-112. https://doi.org/10.1016/j.brainresrev.2010.01.003
  9. Nedergaard M, Verkhratsky A. Artifact versus reality—how astrocytes contribute to synaptic events. Glia. 2012;60(7):1013-1023. https://doi.org/10.1002/glia.22288
  10. Zuchero JB, Barres BA. Glia in mammalian development and disease. Development. 2015;142:3805-3809. https://doi.org/10.1242/dev.129304
  11. Khakh BS, Sofroniew MV. Diversity of astrocyte functions and phenotypes in neural circuits. Nat Neurosci. 2015;18:942-952.
  12. Gray MT, Woulfe JM. Striatal blood-brain barrier permeability in Parkinson’s disease. J Cereb Blood Flow Metab. 2015;35:747-750. https://doi.org/10.1038/jcbfm.2015.32
  13. Herculano-Houzel S. The glia/neuron ratio: how it varies uniformly across brain structures and species and what that means for brain physiology and evolution. Glia. 2014;62:1377-1391. https://doi.org/10.1002/glia.22683
  14. Haydon PG, Nedergaard M. How do astrocytes participate in neural plasticity? Cold Spring Harb Perspect Biol. 2014;7(3):020438. https://doi.org/10.1101/cshperspect.a020438
  15. Zhang Y, Sloan SA, Clarke LE, Caneda C, Plaza CA, Blumenthal PD, Vogel H, Steinberg G, Edwards M, LI G, Duncan J, Cheshier S, Shuer L, Chang E, Grant G, Gephart M, Barres B. Purification and characterization of progenitor and mature human astrocytes reveals transcriptional and functional differences with mouse. Neuron. 2016;89:37-53. https://doi.org/10.1016/j.neuron.2015.11.013
  16. Booth H, Hirst W, Wade-Martins R. The Role of Astrocyte Dysfunction in Parkinson’s Disease Pathogenesis. Trends Neurosci. 2017;40(6):358-370. https://doi.org/10.1016/j.tins.2017.04.001
  17. Jourdain P, Bergersen LH, Bhaukaurally K, Bezzi P, Santello M, Domercq M, Matute C, Tonello F, Gundersen V, Volterra A. Glutamate exocytosis from astrocytes controls synaptic strength. Nature neuroscience. 2007;10(3):331-339. https://doi.org/10.1038/nn1849
  18. Shigetomi E, Patel S, Khakh B. Probing the Complexities of Astrocyte Calcium Signaling. Trends Cell Biol. 2016;26(4):300-312. https://doi.org/10.1016/j.tcb.2016.01.003
  19. Klaassen CD, Aleksunes LM. Xenobiotic, bile acid, and cholesterol transporters: function and regulation. Pharmacological reviews. 2010;62(1):1-96. https://doi.org/10.1124/pr.109.002014
  20. Cox AG. Pharmacogenomics and drug transport/efflux. Concepts in pharmacogenomics. 2010;129-153.
  21. He L, Vasiliou K, Nebert DW. Analysis and update of the human solute carrier (SLC) gene superfamily. Human genomics. 2009;3(2):1. https://doi.org/10.1186/1479-7364-3-2-195
  22. Andrews S. FastQC: a quality control tool for high throughput sequence data. 2010. Accessed August, 21 2017. http://www.bioinformatics.babraham.ac.uk/projects/fastqc
  23. Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30(15):2114-2120. https://doi.org/10.1093/bioinformatics/btu170
  24. Kim D, Pertea G, Trapnell C, Pimentel H, Salzberg R, Steven L. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biology. 2013;14(4):36. https://doi.org/10.1186/gb-2013-14-4-r36
  25. TopHat. A spliced read mapper for RNA-Seq. 2017. Assesed August, 21 2017. https://ccb.jhu.edu/software/tophat/index.shtml
  26. Trapnell C, Trapnell C, Roberts A, Goff L, Pertea G, Kim D, Kelley DR, Pimentel H, Salzberg SL, Rinn JL, Pachter L. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nature protocols. 2012;7(3):562. https://doi.org/10.1038/nprot.2012.016
  27. Anders S, Huber W. Differential expression analysis for sequence count data. Genome biology. 2010;11(10):106. https://doi.org/R106.10.1186/gb-2010-11-10-r106

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