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Neuronal Ryanodine Receptors in Development and Aging

机译:开发和老化中的神经元雷马丁受体

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Ryanodine receptors (RyRs) are intracellular calcium-release channels found on the endoplasmic reticulum of all cells. All three RyR isoforms, RyR1-3, are expressed in the brain, with RyR2 predominating. RyRs are localized within the soma, axons, dendritic spines, and presynaptic terminals of neurons. RyRs are highly expressed in the cerebellum, hippocampus, olfactory region, basal ganglia, and cerebral cortex. During the physiological processes of development and aging, the intracellular calcium homeostasis is largely regulated by RyRs. In this review, we discussed the potential mechanisms underlying development- and age-related RyR regulation. Dysregulation of RyRs can cause imbalance of intracellular calcium levels, leading to cellular vulnerability, impairment of synaptic neuronal function, and eventually neuronal death. Regulation of RyRs may play an essential role in cellular senescence associated with aging, and thus may be pharmacological targets for slowing down aberrant processes and neurodegenerative diseases such as Alzheimer's disease.
机译:瑞尼诺受体(Ryrs)是在所有细胞的内质网上发现的细胞内钙释放通道。所有三个Ryr Isoforms,Ryr1-3都在大脑中表达,Ryr2占主导地位。 RYRS在SOMA,轴突,树突刺和神经元的突触前终端内定位。 Ryrs在小脑,海马,嗅觉区,基底神经节和脑皮层中高度表达。在发育和衰老的生理过程中,细胞内钙稳态在很大程度上受到RYRS的调控。在本次审查中,我们讨论了潜在机制,潜在的发展和年龄相关的RYR规则。 RγRS的失调可能导致细胞内钙水平的不平衡,导致细胞脆弱性,突触神经元功能的损害,最终是神经元死亡。 Ryrs的调节可能在与老化相关的细胞衰老中起重要作用,因此可以是用于减缓异常过程和诸如阿尔茨海默病的神经变性疾病的药理靶标。

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