Expression of functionally distinct ecto-5'-nucleotidase/CD73 glycovariants in reactive astrocytes in experimental autoimmune encephalomyelitis and neuroinflammatory conditions in vitro.


Journal

Glia
ISSN: 1098-1136
Titre abrégé: Glia
Pays: United States
ID NLM: 8806785

Informations de publication

Date de publication:
01 2024
Historique:
revised: 31 07 2023
received: 10 03 2023
accepted: 07 08 2023
medline: 13 11 2023
pubmed: 30 8 2023
entrez: 30 8 2023
Statut: ppublish

Résumé

Ecto-5'-nucleotidase/CD73 (eN/CD73) is a membrane-bound enzyme involved in extracellular production of adenosine and a cell adhesion molecule involved in cell-cell interactions. In neuroinflammatory conditions such as experimental autoimmune encephalomyelitis (EAE), reactive astrocytes occupying active demyelination areas significantly upregulate eN/CD73 and express additional eN/CD73 variants. The present study investigated whether the different eN/CD73 variants represent distinct glycoforms and the functional consequences of their expression in neuroinflammatory states. The study was performed in animals at different stages of EAE and in primary astrocyte cultures treated with a range of inflammatory cytokines. Upregulation at the mRNA, protein, and functional levels, as well as the appearance of multiple eN/CD73 glycovariants were detected in the inflamed spinal cord tissue. At the peak of the disease, eN/CD73 exhibited higher AMP turnover and lower enzyme-substrate affinity than the control group, which was attributed to altered glycosylation under neuroinflammatory conditions. A subsequent in vitro study showed that primary astrocytes upregulated eN/CD73 and expressed the multiple glycovariants upon stimulation with TNFα, IL-1β, IL-6, and ATP, with the effect occurring at least in part via induction of JAK/STAT3 signaling. Experimental removal of glycan moieties from membrane glycoproteins by PNGaseF decreased eN/CD73 activity but had no effect on the enzyme's involvement in astrocyte migration. Our results suggest that neuroinflammatory states are associated with the appearance of functionally distinct eN/CD73 glycovariants, which may play a role in the development of the reactive astrocyte phenotype.

Identifiants

pubmed: 37646205
doi: 10.1002/glia.24459
doi:

Substances chimiques

5'-Nucleotidase EC 3.1.3.5
Adenosine K72T3FS567

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

19-33

Informations de copyright

© 2023 Wiley Periodicals LLC.

Références

Adzic, M., & Nedeljkovic, N. (2018). Unveiling the role of Ecto-5′-Nucleotidase/CD73 in astrocyte migration by using pharmacological tools. Frontiers in Pharmacology, 9(1), 153. https://doi.org/10.3389/fphar.2018.00153
Adzic, M., Stevanovic, I., Josipovic, N., Laketa, D., Lavrnja, I., Bjelobaba, I. M., Bozic, I., Jovanovic, M., Milosevic, M., & Nedeljkovic, N. (2017). Extracellular ATP induces graded reactive response of astrocytes and strengthens their antioxidative defense in vitro. Journal of Neuroscience Research, 95(4), 1053-1066. https://doi.org/10.1002/jnr.23950
Amorini, A. M., Petzold, A., Tavazzi, B., Eikelenboom, J., Keir, G., Belli, A., Giovannoni, G., Di Pietro, V., Polman, C., D'Urso, S., Vagnozzi, R., Uitdehaag, B., & Lazzarino, G. (2009). Increase of uric acid and purine compounds in biological fluids of multiple sclerosis patients. Clinical Biochemistry, 42(10-11), 1001-1006. https://doi.org/10.1016/j.clinbiochem.2009.03.020
Augusto, E., Matos, M., Sévigny, J., El-Tayeb, A., Bynoe, M. S., Müller, C. E., Cunha, R. A., & Chen, J. F. (2013). Ecto-5′-nucleotidase (CD73)-mediated formation of adenosine is critical for the striatal adenosine A2A receptor functions. The Journal of Neuroscience, 33(28), 11390-11399. https://doi.org/10.1523/JNEUROSCI.5817-12.2013
Balasa, R., Barcutean, L., Mosora, O., & Manu, D. (2021). Reviewing the significance of blood-brain barrier disruption in multiple sclerosis pathology and treatment. International Journal of Molecular Sciences, 22(16), 8370. https://doi.org/10.3390/ijms22168370
Barros-Barbosa, A. R., Ferreirinha, F., Oliveira, Â., Mendes, M., Lobo, M. G., Santos, A., Rangel, R., Pelletier, J., Sévigny, J., Cordeiro, J. M., & Correia-de-Sá, P. (2016). Adenosine a(2A)receptor and ecto-5′-nucleotidase/CD73 are upregulated in hippocampal astrocytes of human patients with mesial temporal lobe epilepsy (MTLE). Purinergic Signal, 12(4), 719-734.
Benveniste, E. N., Liu, Y., McFarland, B. C., & Qin, H. (2014). Involvement of the janus kinase/signal transducer and activator of transcription signaling pathway in multiple sclerosis and the animal model of experimental autoimmune encephalomyelitis. Journal of Interferon & Cytokine Research, 34(8), 577-588. https://doi.org/10.1089/jir.2014.0012
Boison, D., Chen, J. F., & Fredholm, B. B. (2010). Adenosine signaling and function in glial cells. Cell Death & Differentiation, 17(7), 1071-1082. https://doi.org/10.1038/cdd.2009.131
Brisevac, D., Bjelobaba, I., Bajic, A., Clarner, T., Stojiljkovic, M., Beyer, C., Andjus, P., Kipp, M., & Nedeljkovic, N. (2012). Regulation of eN (CD73) in cultured cortical astrocytes by different inflammatory factors. Neurochemistry International, 61(5), 681-688. https://doi.org/10.1016/j.neuint.2012.06.017
Carmo, M., Gonçalves, F. Q., Canas, P. M., Oses, J. P., Fernandes, F. D., Duarte, F. V., Palmeira, C. M., Tomé, A. R., Agostinho, P., Andrade, G. M., & Cunha, R. A. (2019). Enhanced ATP release and CD73-mediated adenosine formation sustain adenosine A2A receptor over-activation in a rat model of Parkinson's disease. British Journal of Pharmacology, 176(18), 3666-3680. https://doi.org/10.1111/bph.14771
Cekic, C., & Joel, L. J. (2016). Purinergic regulation of the immune system. Nature Reviews. Immunology, 16(3), 177-192. https://doi.org/10.1038/nri.2016.4
Cunha, R. A. (2016). How does adenosine control neuronal dysfunction and neurodegeneration? Journal of Neurochemistry, 139(6), 1019-1055. https://doi.org/10.1111/jnc.13724
Cunha, R. A., Brendel, P., Zimmermann, H., & Ribeiro, J. A. (2000). Immunologically distinct isoforms of ecto-5′-nucleotidase in nerve terminals of different areas of the rat hippocampus. Journal of Neurochemistry, 74, 334-338.
Cvetko, A., Kifer, D., Gornik, O., Klarić, L., Visser, E., Lauc, G., Wilson, J. F., & Štambuk, T. (2020). Glycosylation alterations in multiple sclerosis show increased Proinflammatory potential. Biomedicine, 8(10), 410. https://doi.org/10.3390/biomedicines8100410
Delmotte, P., Degroote, S., Lafitte, J. J., Lamblin, G., Perini, J. M., & Roussel, P. (2002). Tumor necrosis factor alpha increases the expression of glycosyltransferases and sulfotransferases responsible for the biosynthesis of sialylated and/or sulfated Lewis x epitopes in the human bronchial mucosa. The Journal of Biological Chemistry, 277, 424-431.
Di Virgilio, F., Vultaggio-Poma, V., Falzoni, S., & Giuliani, A. L. (2023). Extracellular ATP: A powerful inflammatory mediator in the central nervous system. Neuropharmacology, 15(224), 109333. https://doi.org/10.1016/j.neuropharm.2022.109333
Domercq, M., Zabala, A., & Matute, C. (2019). Purinergic receptors in multiple sclerosis pathogenesis. Brain Research Bulletin, 151, 38-45. https://doi.org/10.1016/j.brainresbull.2018.11.018
Dragić, M., Zeljković, M., Stevanović, I., Adžić, M., Stekić, A., Mihajlović, K., Grković, I., Ilić, N., Ilić, T. V., Nedeljković, N., & Ninković, M. (2021). Downregulation of CD73/A2AR-mediated adenosine signaling as a potential mechanism of neuroprotective effects of theta-burst transcranial magnetic stimulation in acute experimental autoimmune encephalomyelitis. Brain Sciences, 11(6), 736. https://doi.org/10.3390/brainsci11060736
Eltzschig, H. K., Ibla, J. C., Furuta, G. T., Leonard, M. O., Jacobson, K. A., Enjyoji, K., Robson, S. C., & Colgan, S. P. (2003). Coordinated adenine nucleotide phosphohydrolysis and nucleoside signaling in posthypoxic endothelium: Role of ectonucleotidases and adenosine A2B receptors. The Journal of Experimental Medicine, 198(5), 783-796.
Farina, C., Aloisi, F., & Meinl, E. (2007). Astrocytes are active players in cerebral innate immunity. Trends in Immunology, 28(3), 138-145. https://doi.org/10.1016/j.it.2007.01.005
Fiebich, B. L., Akter, S., & Akundi, R. S. (2014). The two-hit hypothesis for neuroinflammation: Role of exogenous ATP in modulating inflammation in the brain. Frontiers in Cellular Neuroscience, 8(260), 1-11. https://doi.org/10.3389/fncel.2014.00260
Fredholm, B. B. (2007). Adenosine, an endogenous distress signal, modulates tissue damage and repair. Cell Death and Differentiation, 14(7), 1315-1323.
Fredholm, B. B., IJzerman, A. P., Jacobson, K. A., Linden, J., & Müller, C. E. (2011). International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors-an update. Pharmacological Reviews, 63(1), 1-34. https://doi.org/10.1124/pr.110.003285
Gomes, C. V., Kaster, M. P., Tomé, A. R., Agostinho, P. M., & Cunha, R. A. (2011). Adenosine receptors and brain diseases: Neuroprotection and neurodegeneration. Biochimica et Biophysica Acta, 1808(5), 1380-1399. https://doi.org/10.1016/j.bbamem.2010.12.001
Gray, E. G., & Whittaker, V. P. (1962). The isolation of nerve endings from brain: An electron microscopic study of cell fragments derived by homogenizationand centrifugation. Journal of Anatomy, 96, 79-88.
Grkovic, I., Bjelobaba, I., Nedeljkovic, N., Mitrovic, N., Drakulic, D., Stanojlovic, M., & Horvat, A. (2014). Developmental increase in ecto-5′-nucleotidase activity overlaps with appearance of two immunologically distinct enzyme isoforms in rat hippocampal synaptic plasma membranes. Journal of Molecular Neuroscience, 54(1), 109-118. https://doi.org/10.1007/s12031-014-0256-0
Groux-Degroote, S., Krzewinski-Recchi, M. A., Cazet, A., Vincent, A., Lehoux, S., Lafitte, J. J., van Seuningen, I., & Delannoy, P. (2008). IL-6 and IL-8 increase the expression of glycosyltransferases and sulfotransferases involved in the biosynthesis of sialylated and/or sulfated Lewis x epitopes in the human bronchial mucosa. The Biochemical Journal, 410, 213-223.
Haukedal, H., & Freude, K. K. (2021 Jan). Implications of glycosylation in Alzheimer's disease. Frontiers in Neuroscience, 13(14), 625348. https://doi.org/10.3389/fnins.2020.625348
Ingwersen, J., Wingerath, B., Graf, J., Lepka, K., Hofrichter, M., Schröter, F., Wedekind, F., Bauer, A., Schrader, J., Hartung, H. P., Prozorovski, T., & Aktas, O. (2016). Dual roles of the adenosine A2a receptor in autoimmune neuroinflammation. Journal of Neuroinflammation, 26(13), 48. https://doi.org/10.1186/s12974-016-0512-z
Jakovljevic, M., Lavrnja, I., Bozic, I., Milosevic, A., Bjelobaba, I., Savic, D., Sévigny, J., Pekovic, S., Nedeljkovic, N., & Laketa, D. (2019). Induction of NTPDase1/CD39 by reactive microglia and macrophages is associated with the functional state during EAE. Frontiers in Neuroscience, 26(13), 410. https://doi.org/10.3389/fnins.2019.00410
Jakovljevic, M., Lavrnja, I., Bozic, I., Savic, D., Bjelobaba, I., Pekovic, S., Sévigny, J., Nedeljkovic, N., & Laketa, D. (2017). Down-regulation of NTPDase2 and ADP-sensitive P2 Purinoceptors correlate with severity of symptoms during experimental autoimmune encephalomyelitis. Frontiers in Cellular Neuroscience, 30(11), 333. https://doi.org/10.3389/fncel.2017.00333
James, S., & Richardson, P. J. (1993). Production of adenosine from extracellular ATP at the striatal cholinergic synapse. Journal of Neurochemistry, 60(1), 219-227. https://doi.org/10.1111/j.1471-4159.1993.tb05841.x
Keegan, B. M., & Noseworthy, J. H. (2002). Multiple sclerosis. Annual Review of Medicine, 53, 285-302.
Kelley, N., Jeltema, D., Duan, Y., & He, Y. (2019). The NLRP3 Inflammasome: An overview of mechanisms of activation and regulation. International Journal of Molecular Sciences, 20(13), 3328. https://doi.org/10.3390/ijms20133328
Környei, Z., Czirók, A., Vicsek, T., & Madarász, E. (2000). Proliferative and migratory responses of astrocytes to in vitro injury. Journal of Neuroscience Research, 61(4), 421-429. https://doi.org/10.1002/1097-4547(20000815)61:4<421::AID-JNR8>3.0.CO;2-4
Koyama, Y. (2014). Signaling molecules regulating phenotypic conversions of astrocytes and glial scar formation in damaged nerve tissues. Neurochemistry International, 78, 35-42. https://doi.org/10.1016/j.neuint.2014.08.005
Lassmann, H., Bruck, W., & Lucchinetti, C. F. (2007). The immunopathology of multiple sclerosis: An overview. Brain Pathology, 17, 210-218.
Lavrnja, I., Bjelobaba, I., Stojiljkovic, M., Pekovic, S., Mostarica-Stojkovic, M., Stosic-Grujicic, S., & Nedeljkovic, N. (2009). Time-course changes in ectonucleotidase activities during experimental autoimmune encephalomyelitis. Neurochemistry International, 55(4), 193-198. https://doi.org/10.1016/j.neuint.2009.02.013
Lavrnja, I., Laketa, D., Savic, D., Bozic, I., Bjelobaba, I., Pekovic, S., & Nedeljkovic, N. (2015). Expression of a second ecto-5′-nucleotidase variant besides the usual protein in symptomatic phase of experimental autoimmune encephalomyelitis. Journal of Molecular Neuroscience, 55(4), 898-911. https://doi.org/10.1007/s12031-014-0445-x
Lavrnja, I., Stojkov, D., Bjelobaba, I., Pekovic, S., Dacic, S., Nedeljkovic, N., Mostarica-Stojkovic, M., Stosic-Grujicic, S., Rakic, L., & Stojiljkovic, M. (2008). Ribavirin ameliorates experimental autoimmune encephalomyelitis in rats and modulates cytokine production. International Immunopharmacology, 8(9), 1282-1290. https://doi.org/10.1016/j.intimp.2008.05.008
Le Feuvre, R., Brough, D., & Rothwell, N. (2002). Extracellular ATP and P2X7 receptors in neurodegeneration. European Journal of Pharmacology, 447(2-3), 261-269. https://doi.org/10.1016/s0014-2999(02)01848-4
Liang, C. C., Park, A. Y., & Guan, J. L. (2007). In vitro scratch assay: A convenient and inexpensive method for analysis of cell migration in vitro. Nature Protocols, 2(2), 329-333. https://doi.org/10.1038/nprot.2007.30
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W. S., Peterson, T. C., Wilton, D. K., Frouin, A., Napier, B. A., Panicker, N., Kumar, M., Buckwalter, M. S., Rowitch, D. H., Dawson, V. L., Dawson, T. M., … Barres, B. A. (2017). Neurotoxic reactive astrocytes are induced by activated microglia. Nature, 541(7638), 481-487. https://doi.org/10.1038/nature21029
Matute, C. (2011). Glutamate and ATP signalling in white matter pathology. Journal of Anatomy, 219, 53-64.
Mehul, B., Aubery, M., Mannherz, H. G., & Codogno, P. (1993). Dual mechanism of laminin modulation of eN activity. Journal of Cellular Biochemistry, 52(3), 266-274. https://doi.org/10.1002/jcb.240520303
Mills, J. H., Thompson, L. F., Mueller, C., Waickman, A. T., Jalkanen, S., Niemela, J., Airas, L., & Bynoe, M. S. (2008). CD73 is required for efficient entry of lymphocytes into the central nervous system during experimental autoimmune encephalomyelitis. PNAS, 105, 9325-9330.
Misumi, Y., Ogata, S., Hirose, S., & Ikehara, Y. (1990). Primary structure of rat liver 5′-nucleotidase deduced from the cDNA. Presence of the COOH-terminal hydrophobic domain for possible posttranslational modification by glycophospholipid.J. Biological Chemistry, 265, 2178-2183.
Mkhikian, H., Grigorian, A., Li, C. F., Chen, H. L., Newton, B., Zhou, R. W., Beeton, C., Torossian, S., Tatarian, G. G., Lee, S. U., Lau, K., Walker, E., Siminovitch, K. A., Chandy, K. G., Yu, Z., Dennis, J. W., & Demetriou, M. (2011). Genetics and the environment converge to dysregulate N-glycosylation in multiple sclerosis. Nature Communications, 2, 334. https://doi.org/10.1038/ncomms1333
Nedeljkovic, N. (2019). Complex regulation of ecto-5′-nucleotidase/CD73 and A2AR-mediated adenosine signaling at neurovascular unit: A link between acute and chronic neuroinflammation. Pharmacological Research, 144, 99-115. https://doi.org/10.1016/j.phrs.2019.04.007
Nedeljković, N., Nikezić, G., Horvat, A., Peković, S., Stojiljković, M., & Martinović, J. V. (1998). Properties of Mg(2+)-ATPase rat brain synaptic plasma membranes. General Physiology and Biophysics, 17(1), 3-13.
Olmo, N., Turnay, J., Risse, G., Deutzmann, R., von der Mark, K., & Lizarbe, M. A. (1992). Modulation of 5′-nucleotidase activity in plasma membranes and intact cells by the extracellular matrix proteins laminin and fibronectin. The Biochemical Journal, 282(Pt 1), 181-188.
Patil, V., Bohara, R., Winter, C., Kilcoyne, M., McMahon, S., & Pandit, A. (2023). An insight into new glycotherapeutics in glial inflammation: Understanding the role of glycosylation in mitochondrial function and acute to the chronic phases of inflammation. CNS Neuroscience & Therapeutics, 29(1), 429-444. https://doi.org/10.1111/cns.14016
Plastini, M. J., Desu, H. L., & Brambilla, R. (2020). Dynamic responses of microglia in animal models of multiple sclerosis. Frontiers in Cellular Neuroscience, 20(14), 269. https://doi.org/10.3389/fncel.2020.00269
Rebelo, A. L., Gubinelli, F., Roost, P., Jan, C., Brouillet, E., Van Camp, N., Drake, R. R., Saldova, R., & Pandit, A. (2021). Complete spatial characterisation of N-glycosylation upon striatal neuroinflammation in the rodent brain. Journal of Neuroinflammation, 18(1), 116. https://doi.org/10.1186/s12974-021-02163-6
Reily, C., Stewart, T. J., Renfrow, M. B., & Novak, J. (2019). Glycosylation in health and disease. Nature Reviews. Nephrology, 15(6), 346-366. https://doi.org/10.1038/s41581-019-0129-4
Resta, R., Hooker, S. W., Hansen, K. R., Laurent, A. B., Park, J. L., Blackburn, M. R., Knudsen, T. B., & Thompson, L. F. (1993). Murine ecto-5′-nucleotidase (CD73): cDNA cloning and tissue distribution. Gene, 133(2), 171-177.
Rissanen, E., Virta, J. R., Paavilainen, T., Tuisku, J., Helin, S., Luoto, P., Parkkola, R., Rinne, J. O., & Airas, L. (2013). Adenosine A2A receptors in secondary progressive multiple sclerosis: A [(11)C]TMSX brain PET study. Journal of Cerebral Blood Flow & Metabolism, 33(9), 1394-1401. https://doi.org/10.1038/jcbfm.2013.85
Rott, O., Fleischer, B., & Cash, E. (1994). Interleukin-10 prevents experimental allergic encephalomyelitis in rats. European Journal of Immunology, 24(6), 1434-1440. https://doi.org/10.1002/eji.1830240629
Sadej, R., Inai, K., Rajfur, Z., Ostapkowicz, A., Kohler, J., Skladanowski, A. C., Mitchell, B. S., & Spychala, J. (2008). Tenascin C interacts with eN (eN) and regulates adenosine generation in cancer cells. Biochimica et Biophysica Acta, 1782(1), 35-40. https://doi.org/10.1016/j.bbadis.2007.11.001
Sadej, R., & Skladanowski, A. C. (2012). Dual, enzymatic and non-enzymatic, function of eN (eN, CD73) in migration and invasion of A375 melanoma cells. Acta Biochimica Polonica, 59(4), 647-652.
Shen, Y., Sun, A., Wang, Y., Cha, D., Wang, H., Wang, F., Feng, L., Fang, S., & Shen, Y. (2012). Upregulation of mesencephalic astrocyte-derived neurotrophic factor in glial cells is associated with ischemia-induced glial activation. Journal of Neuroinflammation, 23(9), 254. https://doi.org/10.1186/1742-2094-9-254
Spychala, J., Zimmermann, A. G., & Mitchell, B. S. (1999). Tissue-specific regulation of the ecto-5′-nucleotidase promoter. Role of the camp response element site in mediating repression by the upstream regulatory region. The Journal of Biological Chemistry, 274(32), 22705-22712.
Vainchtein, I. D., & Molofsky, A. V. (2020). Astrocytes and microglia: In sickness and in health. Trends in Neurosciences, 43(3), 144-154. https://doi.org/10.1016/j.tins.2020.01.003
Villar-Menéndez, I., Porta, S., Buira, S. P., Pereira-Veiga, T., Díaz-Sánchez, S., Albasanz, J. L., Ferrer, I., Martín, M., & Barrachina, M. (2014). Increased striatal adenosine A2A receptor levels is an early event in Parkinson's disease-related pathology and it is potentially regulated by miR-34b. Neurobiology of Disease, 69, 206-214. https://doi.org/10.1016/j.nbd.2014.05.030
Vogel, M., Kowalewski, H., Zimmermann, H., Hooper, N. M., & Turner, A. J. (1992). Soluble low-km 5′-nucleotidase from electric-ray (Torpedo marmorata) electric organ and bovine cerebral cortex is derived from the glycosyl-phosphatidylinositol-anchoredectoenzyme by phospholipase C cleavage. The Biochemical Journal, 284(Pt 3), 621-624.
Wada, I., Himeno, M., Furuno, K., & Kato, K. (1986). Biosynthesis and intracellular transport of rat liver 5′-nucleotidase. The Journal of Biological Chemistry, 261, 2222-2227.
Wheeler, M. A., Clark, I. C., Tjon, E. C., Li, Z., Zandee, S. E. J., Couturier, C. P., Watson, B. R., Scalisi, G., Alkwai, S., Rothhammer, V., Rotem, A., Heyman, J. A., Thaploo, S., Sanmarco, L. M., Ragoussis, J., Weitz, D. A., Petrecca, K., Moffitt, J. R., Becher, B., & Quintana, F. J. (2020). MAFG-driven astrocytes promote CNS inflammation. Nature, 578(7796), 593-599. https://doi.org/10.1038/s41586-020-1999-0
Wiese, S., Karus, M., & Faissner, A. (2012). Astrocytes as a source for extracellular matrix molecules and cytokines. Frontiers in Pharmacology, 3, 120. https://doi.org/10.3389/fphar.2012.00120
Yue, Y., Stone, S., & Lin, W. (2018). Role of nuclear factor κB in multiple sclerosis and experimental autoimmune encephalomyelitis. Neural Regeneration Research, 13(9), 1507-1515. https://doi.org/10.4103/1673-5374.237109
Zamanian, J. L., Xu, L., Foo, L. C., Nouri, N., Zhou, L., Giffard, R. G., & Barres, B. A. (2012). Genomic analysis of reactive astrogliosis. The Journal of Neuroscience, 32(18), 6391-6410. https://doi.org/10.1523/JNEUROSCI.6221-11.2012
Zheng, W., Feng, Y., Zeng, Z., Ye, M., Wang, M., Liu, X., Tang, P., Shang, H., Sun, X., Lin, X., Wang, M., Li, Z., Weng, Y., Guo, W., Vakal, S., & Chen, J. F. (2022 Feb 18). Choroid plexus-selective inactivation of adenosine A2A receptors protects against T cell infiltration and experimental autoimmune encephalomyelitis. Journal of Neuroinflammation, 19(1), 52. https://doi.org/10.1186/s12974-022-02415-z
Zimmermann, H. (1992). 5′-Nucleotidase-Molecular structure and functional aspects. The Biochemical Journal, 285, 345-365.
Zimmermann, H., Zebisch, M., & Sträter, N. (2012). Cellular function and molecular structure of ecto-nucleotidases. Purinergic Signal, 8(3), 437-502. https://doi.org/10.1007/s11302-012-9309-4
Zrzavy, T., Hametner, S., Wimmer, I., Butovsky, O., Weiner, H. L., & Lassmann, H. (2017). Loss of “homeostatic” microglia and patterns of their activation in active multiple sclerosis. Brain, 140(7), 1900-1913. https://doi.org/10.1093/brain/awx113

Auteurs

Marija Adzic Bukvic (M)

Laboratory for Neurobiology, Department of General Physiology and Biophysics, Faculty of Biology, University of Belgrade, Belgrade, Serbia.

Danijela Laketa (D)

Laboratory for Neurobiology, Department of General Physiology and Biophysics, Faculty of Biology, University of Belgrade, Belgrade, Serbia.

Milorad Dragic (M)

Laboratory for Neurobiology, Department of General Physiology and Biophysics, Faculty of Biology, University of Belgrade, Belgrade, Serbia.

Irena Lavrnja (I)

Institute for Biological Research "Sinisa Stankovic"-National Institute of the Republic of Serbia, University of Belgrade, Belgrade, Serbia.

Nadezda Nedeljkovic (N)

Laboratory for Neurobiology, Department of General Physiology and Biophysics, Faculty of Biology, University of Belgrade, Belgrade, Serbia.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH