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纹状体信号复合物组织中的功能可塑性。

Functional plasticity in the organization of signaling complexes in the striatum.

作者信息

Allen Patrick B

机构信息

Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06508, USA.

出版信息

Parkinsonism Relat Disord. 2004 Jul;10(5):287-92. doi: 10.1016/j.parkreldis.2004.02.016.

Abstract

Dopamine plays a prominent role in regulating fast synaptic transmission in the striatum. Following dopamine receptor stimulation, various signal transduction pathways are activated, leading to the altered phosphorylation state and functional activity of substrate proteins, including glutamate-gated ion channels. Protein phosphatase 1 (PP1) plays a central role in these events. Recent studies have revealed a system for targeting PP1 to specific substrates in dendritic spines, via association with the cytoskeletal scaffolding proteins, spinophilin and neurabin. Interactions between these proteins and the actin cytoskeleton are dynamically regulated by the cAMP pathway, and thus play a role in dopamine-mediated striatal plasticity.

摘要

多巴胺在调节纹状体中的快速突触传递方面发挥着重要作用。多巴胺受体受到刺激后,各种信号转导通路被激活,导致底物蛋白(包括谷氨酸门控离子通道)的磷酸化状态和功能活性发生改变。蛋白磷酸酶1(PP1)在这些事件中起核心作用。最近的研究揭示了一种通过与细胞骨架支架蛋白、亲肌动蛋白和神经肌动蛋白结合,将PP1靶向树突棘中特定底物的系统。这些蛋白与肌动蛋白细胞骨架之间的相互作用受cAMP途径动态调节,因此在多巴胺介导的纹状体可塑性中发挥作用。

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