АСТРОЦИТЫ И ПЛАСТИЧНОСТЬ СИНАПСОВ. ЧАСТЬ II. ВНЕКЛЕТОЧНЫЙ МАТРИКС И ПЕРИНЕЙРОНАЛЬНАЯ СЕТЬ
- Авторы: Швалев В.Н.1, Сосунов А.А.2, Челышев Ю.А.3
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Учреждения:
- Национальный медицинский исследовательский центр кардиологии
- Колумбийский университет
- Казанский государственный медицинский университет
- Выпуск: Том L, № 3 (2018)
- Страницы: 38-43
- Раздел: Статьи
- URL: https://journals.rcsi.science/1027-4898/article/view/14132
- DOI: https://doi.org/10.17816/nb14132
- ID: 14132
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Рассмотрено участие астроцитов в образовании внеклеточного матрикса (ВКМ) ЦНС, значение ВКМ и его специализированной формы, перинейрональной сети, в синаптогенезе и пластичности синапсов в зрелом мозге. В аспекте понимания механизмов шизофрении приведены данные об элиминации и пластичности синапсов, роли молекул комплемента и некоторых генов риска, которые экспрессируются астроцитами и влияют на синаптогенез и функцию синапсов.
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Вадим Николаевич Швалев
Национальный медицинский исследовательский центр кардиологии
Email: vadim.shvalev@mail.ru
121552, г. Москва, 3-я Черепковская, д. 15А
Александр Алексеевич Сосунов
Колумбийский университет
Email: aas190@cumc.columbia.edu
Нью-Йорк, 10032, США
Юрий Александрович Челышев
Казанский государственный медицинский университет
Email: chelyshev-kzn@yandex.ru
420012, г. Казань, ул. Бутлерова, д. 49
Список литературы
- Baroncelli L., Scali M., Sansevero G. et al. Experience affects critical period plasticity in the visual cortex through an epigenetic regulation of histone post-translational modifications // J Neurosci. 2016. Vol. 36, № 12. P. 3430-3440.
- Bartoletti A., Medini P., Berardi N., Maffei L. Environmental enrichment prevents effects of dark-rearing in the rat visual cortex // Nat Neurosci. 2004. Vol. 7, № 3. P. 215-216.
- Blumcke I., Thom M., Aronica E. et al. International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: a task force report from the ILAE commission on diagnostic methods // Epilepsia. 2013. Vol. 54, № 7. P. 1315-1329.
- Brakebusch C., Seidenbecher C.I., Asztely F. et al. Brevican-deficient mice display impaired hippocampal CA1 long-term potentiation but show no obvious deficits in learning and memory // Mol Cell Biol. 2002. Vol. 22. P. 7417-7427.
- Brandon N.J., Millar J.K., Korth C. et al. Understanding the role of DISC1 in psychiatric disease and during normal development // J Neurosci. 2009. Vol.29. P. 12768-12775.
- Carstens K.E., Phillips M.L., Pozzo-Miller L. et al. Perineuronal Nets Suppress Plasticity of Excitatory Synapses on CA2 Pyramidal Neurons // J Neurosci. 2016. Vol. 36, № 23. P. 6312-6320.
- Carulli D., Pizzorusso T., Kwok J.C. et al. Animals lacking link protein have attenuated perineuronal nets and persistent plasticity // Brain. 2010. Vol. 133, № 8. P. 2331-2347.
- Chen N., Bao Y., Xue Y. et al. Meta-analyses of RELN variants in neuropsychiatric disorders // Behav Brain Res. 2017. Vol. 332. P. 110-119.
- Czipri M., Otto J.M., Cs-Szabo G. et al. Genetic rescue of chondrodysplasia and the perinatal lethal effect of cartilage link protein deficiency // J Biol Chem. 2003. Vol. 278, № 40. P. 39214-39223.
- Dauth S., Grevesse T., Pantazopoulos H. et al. Extracellular matrix protein expression is brain region dependent // J Comp Neurol. 2016. Vol. 524, № 7. P. 1309-1336.
- Deepa S.S., Carulli D., Galtrey C. et al. Composition of perineuronal net extracellular matrix in rat brain: a different disaccharide composition for the net-associated proteoglycans // J Biol Chem. 2006. Vol. 281, № 26. P. 17789-17800.
- Dudek S.M., Alexander G.M., Farris S. Rediscovering area CA2: unique properties and functions // Nat Rev Neurosci. 2016. Vol. 17, № 2. P. 89-102.
- Ebrahimi M., Yamamoto Y., Sharifi K. et al. Astrocyte-expressed FABP7 regulates dendritic morphology and excitatory synaptic function of cortical neurons // Glia. 2016. Vol. 64. P. 48-62.
- Escudero-Esparza A., Kalchishkova N., Kurbasic E. et al. The novel complement inhibitor human CUB and Sushi multiple domains 1 (CSMD1) protein promotes factor I-mediated degradation of C4b and C3b and inhibits the membrane attack complex assembly // FASEB J. 2013. Vol. 27. P. 5083-5093.
- Fagiolini M., Hensch T.K. Inhibitory threshold for critical-period activation in primary visual cortex // Nature. 2000. Vol. 404, № 6774. P. 183-186.
- Favuzzi E., Marques-Smith A., Deogracias R. et al. Activity-dependent gating of parvalbumin interneuron function by the perineuronal net protein brevican // Neuron. 2017. Vol. 95. P. 639-655.
- Fisher D., Xing B., Dill J. et al. Leukocyte common antigen-related phosphatase is a functional receptor for chondroitin sulfate proteoglycan axon growth inhibitors // J Neurosci. 2011. Vol. 31(40). P. 14051-14066.
- Fowke T.M., Karunasinghe R.N., Bai J.Z. et al. Hyaluronan synthesis by developing cortical neurons in vitro // Sci Rep. 2017. Vol. 7. P. 44135.
- Frischknecht R., Heine M., Perrais D. et al. Brain extracellular matrix affects AMPA receptor lateral mobility and short-term synaptic plasticity // Nat Neurosci. 2009. Vol. 12. P. 897-904.
- Gasque P., Dean Y.D., McGreal E.P. et al. Complement components of the innate immune system in health and disease in the CNS // Immunopharmacology. 2000. Vol. 49. P. 171-186.
- Gogolla N., Caroni P., Luthi A., Herry C. Perineuronal nets protect fear memories from erasure. Science. 2009. Vol. 325, № 5945. P. 1258-1261.
- Gurevicius K., Kuang.F, Stoenica L. et al. Genetic ablation of tenascin-C expression leads to abnormal hippocampal CA1 structure and electrical activity in vivo // Hippocampus. 2009. Vol. 19. P. 1232-1246.
- Harauzov A., Spolidoro M., DiCristo G. et al. Reducing intracortical inhibition in the adult visual cortex promotes ocular dominance plasticity // J Neurosci. 2010. Vol. 30, № 1. P. 361-371.
- Hardingham G.E., Do K.Q. Linking early-life NMDAR hypofunction and oxidative stress in schizophrenia pathogenesis // Nat Rev Neurosci. 2016. Vol. 17. P. 125-134.
- Irintchev A., Rollenhagen A., Troncoso E. et al. Structural and functional aberrations in the cerebral cortex of tenascin-C deficient mice // Cereb Cortex. 2005. Vol. 15. P. 950-962.
- Kim R., Sepulveda-Orengo M.T., Healey K.L. et al. Regulation of glutamate transporter 1 (GLT-1) gene expression by cocaine self-administration and withdrawal // Neuropharmacology. 2018. Vol. 128. P. 1-10.
- Kochlamazashvili G., Henneberger C., Bukalo O. et al. The extracellular matrix molecule hyaluronic acid regulates hippocampal synaptic plasticity by modulating postsynaptic L-type Ca(2+) channels // Neuron. 2010. Vol. 67. P. 116-128.
- Kolluri N., Sun Z., Sampson A.R., Lewis D.A. Lamina-specific reductions in dendritic spine density in the prefrontal cortex of subjects with schizophrenia // Am J Psychiatry. 2005. Vol. 162. P. 1200-1202.
- Lensjo K.K., Christensen A.C., Tennoe S. et al. Differential expression and cell-type specificity of perineuronal nets in hippocampus, medial entorhinal cortex, and visual cortex examined in the rat and mouse // eNeuro. 2017. Vol. 4. P. 3.
- Lensjo K.K., Lepperod M.E., Dick G. et al. Removal of perineuronal nets unlocks juvenile plasticity through network mechanisms of decreased inhibition and increased gamma activity // J Neurosci. 2017. Vol. 37, № 5. P. 1269-1283.
- Mayilyan K.R., Weinberger D.R., Sim R.B. The complement system in schizophrenia // Drug News Perspect. 2008. Vol. 21. P. 200-210.
- Morawski M., Reinert T., Meyer-Klaucke W. et al. Ion exchanger in the brain: Quantitative analysis of perineuronally fixed anionic binding sites suggests diffusion barriers with ion sorting properties // Sci Rep. 2015. Vol. 5. P. 16471.
- Morellini F., Sivukhina E., Stoenica L. et al. Improved reversal learning and working memory and enhanced reactivity to novelty in mice with enhanced GABAergic innervation in the dentate gyrus // Cereb Cortex. 2010. Vol. 20. P. 2712-2727.
- Nicholson C., Sykova E. Extracellular space structure revealed by diffusion analysis // Trends Neurosci. 1998. Vol. 21, № 5. P. 207-215.
- Pantazopoulos H., Woo T.U., Lim M.P. et al. Extracellular matrix-glial abnormalities in the amygdala and entorhinal cortex of subjects diagnosed with schizophrenia // Arch Gen Psychiatry. 2010. Vol. 67. P. 155-166.
- Pizzorusso T., Medini P., Berardi N. et al. Reactivation of ocular dominance plasticity in the adult visual cortex // Science. 2002. Vol. 298, № 5596. P. 1248-1251.
- Romberg C., Yang S., Melani R. et al. Depletion of perineuronal nets enhances recognition memory and long-term depression in the perirhinal cortex // J Neurosci. 2013. Vol. 33. 7057-7065.
- Selemon L.D., Zecevic N. Schizophrenia: a tale of two critical periods for prefrontal cortical development // Transl Psychiatry. 2015. Vol. 5. e623.
- Shen Y., Tenney A.P., Busch S.A. et al. PTPsigma is a receptor for chondroitin sulfate proteoglycan, an inhibitor of neural regeneration // Science. 2009. Vol. 326. P. 592-596.
- Shimamoto C., Ohnishi T., Maekawa M. et al. Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies // Hum Mol Genet. 2014. Vol. 23. P. 6495-6511.
- Sloviter R.S. Permanently altered hippocampal structure, excitability, and inhibition after experimental status epilepticus in the rat: the “dormant basket cell” hypothesis and its possible relevance to temporal lobe epilepsy // Hippocampus. 1991. Vol. 1, № 1. P. 41-66.
- Smith C.C., Mauricio R., Nobre L. et al. Differential regulation of perineuronal nets in the brain and spinal cord with exercise training // Brain Res Bull. 2015. Vol. 111. P. 20-26.
- Song I., Dityatev A. Crosstalk between glia, extracellular matrix and neurons // Brain Res Bull. 2018. Vol. 136. P. 101-108.
- Stamenkovic V., Milenkovic I., Galjak N. et al. Enriched environment alters the behavioral profile of tenascin-C deficient mice // Behav Brain Res. 2017. Vol. 331. P. 241-253.
- Steen V.M., Nepal C., Ersland K.M. et al. Neuropsychological deficits in mice depleted of the schizophrenia susceptibility gene CSMD1 // PLoS One. 2013. Vol. 8. e79501.
- Suttkus A., Rohn S., Weigel S. et al. Aggrecan, link protein and tenascin-R are essential components of the perineuronal net to protect neurons against iron-induced oxidative stress // Cell Death Dis. 2014. Vol. 5. P. 1119.
- Tanahashi S., Yamamura S., Nakagawa M. et al. Clozapine, but not haloperidol, enhances glial D-serine and L-glutamate release in rat frontal cortex and primary cultured astrocytes // Br J Pharmacol. 2012. Vol. 165. P. 1543-1555.
- Thompson E.H., Lensjo K.K., Wigestrand M.B. et al. Removal of perineuronal nets disrupts recall of a remote fear memory // Proc Natl Acad Sci U S A. 2018. Vol. 115, № 3. P. 607-612.
- Tomasi D., Volkow N.D. Mapping small-world properties through development in the human brain: disruption in schizophrenia // PLoS One. 2014. Vol. 9. e96176.
- Wasser C.R., Herz J. Reelin: Neurodevelopmental architect and homeostatic regulator of excitatory synapses // J Biol Chem. 2017. Vol. 292. P. 1330-1338.
- Watanabe A., Toyota T., Owada Y. et al. Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotyp // PLoS Biol. 2007. Vol. 5. e297.
- Watanabe H., Yamada Y. Chondrodysplasia of gene knockout mice for aggrecan and link protein // Glycoconj J. 2002. Vol. 19, № 4. P. 269-273.
- Watanabe H., Yamada Y. Mice lacking link protein develop dwarfism and craniofacial abnormalities // Nat Genet. 1999. Vol. 21, № 2. P. 225-229.
- Weber P., Bartsch U., Rasband M.N. et al. Mice deficient for tenascin-R display alterations of the extracellular matrix and decreased axonal conduction velocities in the CNS // J Neurosci. 1999. Vol. 19. P. 4245-4262.
- Wiesel T.N., Hubel D.H. Extent of recovery from the effects of visual deprivation in kittens // J Neurophysiol. 1965. Vol. 28, № 6. P. 1060-1072.
- Wittner L., Huberfeld G., Clemenceau S. et al. The epileptic human hippocampal cornu ammonis 2 region generates spontaneous interictal-like activity in vitro // Brain. 2009. Vol. 132, № 11. P. 3032-3046.
- Woo T.U. Neurobiology of schizophrenia onset. // Curr Top Behav Neurosci. 2014. Vol. 16. P. 267-295.