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A3 腺苷受体介导少突胶质细胞死亡和视神经缺血损伤。

A3 Adenosine receptors mediate oligodendrocyte death and ischemic damage to optic nerve.

机构信息

CIBERNED, Achucarro Basque Center for Neuroscience and Departamento de Neurociencias, Universidad del País Vasco (UPV/EHU), E-48940, Leioa, Spain.

出版信息

Glia. 2014 Feb;62(2):199-216. doi: 10.1002/glia.22599. Epub 2013 Dec 6.

DOI:10.1002/glia.22599
PMID:24311446
Abstract

Adenosine receptor activation is involved in myelination and in apoptotic pathways linked to neurodegenerative diseases. In this study, we investigated the effects of adenosine receptor activation in the viability of oligodendrocytes of the rat optic nerve. Selective activation of A3 receptors in pure cultures of oligodendrocytes caused concentration-dependent apoptotic and necrotic death which was preceded by oxidative stress and mitochondrial membrane depolarization. Oligodendrocyte apoptosis induced by A3 receptor activation was caspase-dependent and caspase-independent. In addition to dissociated cultures, incubation of optic nerves ex vivo with adenosine and the A3 receptor agonist 2-CI-IB-MECA(1-[2-Chloro-6-[[(3-iodophenyl)methyl]amino]-9H-purin-9-yl]-1-deoxy-N-methyl-b-D-ribofuranuronamide)-induced caspase-3 activation, oligodendrocyte damage, and myelin loss, effects which were prevented by the presence of caffeine and the A3 receptor antagonist MRS 1220 (N-[9-Chloro-2-(2-furanyl)[1,2,4]-triazolo [1,5-c]quinazolin-5-yl]benzene acetamide). Finally, ischemia-induced injury and functional loss to the optic nerve was attenuated by blocking A3 receptors. Together, these results indicate that adenosine may trigger oligodendrocyte death via activation of A3 receptors and suggest that this mechanism contributes to optic nerve and white matter ischemic damage.

摘要

腺苷受体的激活参与髓鞘形成和与神经退行性疾病相关的凋亡途径。在这项研究中,我们研究了腺苷受体激活对大鼠视神经少突胶质细胞活力的影响。在纯少突胶质细胞培养物中,选择性激活 A3 受体导致浓度依赖性的凋亡和坏死死亡,这之前是氧化应激和线粒体膜去极化。A3 受体激活诱导的少突胶质细胞凋亡依赖于半胱天冬酶和不依赖半胱天冬酶。除了分离培养物外,体外孵育视神经与腺苷和 A3 受体激动剂 2-CI-IB-MECA(1-[2-氯-6-[[(3-碘苯基)甲基]氨基]-9H-嘌呤-9-基]-1-脱氧-N-甲基-β-D-核糖呋喃尿苷酰胺)可诱导半胱天冬酶-3 激活、少突胶质细胞损伤和髓鞘丢失,这些作用可被咖啡因和 A3 受体拮抗剂 MRS 1220(N-[9-氯-2-(2-呋喃基)[1,2,4]-三唑[1,5-c]喹唑啉-5-基]苯乙酰胺)阻止。最后,通过阻断 A3 受体,可减轻缺血引起的视神经损伤和功能丧失。总之,这些结果表明,腺苷可能通过激活 A3 受体引发少突胶质细胞死亡,并表明该机制有助于视神经和白质缺血性损伤。

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