探索 AMPA 受体辅助蛋白在突触功能和疾病中的作用。

Mohammad Qneibi, Sosana Bdir, Mohammad Bdair, Samia Ammar Aldwaik, Maram Heeh, Dana Sandouka, Tala Idais
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摘要

α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)离子型谷氨酸受体(AMPARs)在哺乳动物大脑中介导快速兴奋性突触传递,主要由神经递质谷氨酸驱动。AMPAR 的活性,尤其是钙离子渗透性 AMPAR(CP-AMPAR)的活性,受到各种辅助亚基的重要影响。这些亚基是与受体核心结合的整体膜蛋白,可改变受体的功能特性,包括离子通道动力学和受体迁移。这篇综述对所有已知的 AMPAR 辅助蛋白进行了全面编目,提供了有关突触调节生化机制的重要见解,以及 CP-AMPAR 与其钙离子渗透性 AMPA 受体(CI-AMPAR)相比的特殊影响。了解不同脑区的 AMPARs 及其辅助亚基之间复杂的相互作用对于阐明它们在学习和记忆等认知功能中的作用至关重要。重要的是,这些辅助蛋白的表达、功能或相互作用的改变与各种神经系统疾病有关。尤其是通过 CP-AMPARs 发出的异常信号与神经发育、神经退行性和精神疾病中严重的突触功能障碍有关。针对 AMPAR 辅助亚基复合物的不同特性,尤其是涉及 CP-AMPARs 的复合物,可以发现新的治疗策略,从而有可能在治疗复杂的神经元疾病时采取更精确的干预措施。
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Exploring the role of AMPA receptor auxiliary proteins in synaptic functions and diseases.

α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) ionotropic glutamate receptors (AMPARs) mediate rapid excitatory synaptic transmission in the mammalian brain, primarily driven by the neurotransmitter glutamate. The modulation of AMPAR activity, particularly calcium-permeable AMPARs (CP-AMPARs), is crucially influenced by various auxiliary subunits. These subunits are integral membrane proteins that bind to the receptor's core and modify its functional properties, including ion channel kinetics and receptor trafficking. This review comprehensively catalogs all known AMPAR auxiliary proteins, providing vital insights into the biochemical mechanisms governing synaptic modulation and the specific impact of CP-AMPARs compared to their calcium-impermeable AMPA receptor (CI-AMPARs). Understanding the complex interplay between AMPARs and their auxiliary subunits in different brain regions is essential for elucidating their roles in cognitive functions such as learning and memory. Importantly, alterations in these auxiliary proteins' expression, function or interactions have been implicated in various neurological disorders. Aberrant signaling through CP-AMPARs, in particular, is associated with severe synaptic dysfunctions across neurodevelopmental, neurodegenerative and psychiatric conditions. Targeting the distinct properties of AMPAR-auxiliary subunit complexes, especially those involving CP-AMPARs, could disclose new therapeutic strategies, potentially allowing for more precise interventions in treating complex neuronal disorders.

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