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Role of Microglia Adenosine A2A Receptors in Retinal and Brain Neurodegenerative Diseases

机译:小胶质细胞腺苷A2A受体在视网膜和脑神经退行性疾病中的作用

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摘要

Neuroinflammation mediated by microglial cells in the brain has been commonly associated with neurodegenerative diseases. Whether this microglia-mediated neuroinflammation is cause or consequence of neurodegeneration is still a matter of controversy. However, it is unequivocal that chronic neuroinflammation plays a role in disease progression and halting that process represents a potential therapeutic strategy. The neuromodulator adenosine emerges as a promising targeting candidate based on its ability to regulate microglial proliferation, chemotaxis, and reactivity through the activation of its G protein coupled A2A receptor (A2AR). This is in striking agreement with the ability of A2AR blockade to control several brain diseases. Retinal degenerative diseases have been also associated with microglia-mediated neuroinflammation, but the role of A2AR has been scarcely explored. This review aims to compare inflammatory features of Parkinson's and Alzheimer's diseases with glaucoma and diabetic retinopathy, discussing the therapeutic potential of A2AR in these degenerative conditions.
机译:由脑中的小胶质细胞介导的神经炎症通常与神经退行性疾病有关。这种小胶质细胞介导的神经炎症是神经退行性变的原因还是后果仍是一个有争议的问题。然而,毫无疑问的是,慢性神经炎症在疾病进展中起着一定作用,而中止这一过程代表了一种潜在的治疗策略。基于神经调节剂腺苷通过激活其G蛋白偶联的A2A受体(A2AR)来调节小胶质细胞增殖,趋化性和反应性的能力,它成为有前途的靶向候选物。这与A2AR阻滞控制几种脑部疾病的能力非常吻合。视网膜退行性疾病也与小胶质细胞介导的神经炎症有关,但很少探讨A2AR的作用。这篇综述旨在比较帕金森氏症和阿尔茨海默氏症与青光眼和糖尿病性视网膜病变的炎症特征,讨论A2AR在这些退行性疾病中的治疗潜力。

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