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Regulation of 5-HT2A serotonin receptor sorting and signaling in cortical pyramidal neurons.

机译:皮质锥体神经元中5-HT2A血清素受体分类和信号传导的调节。

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摘要

The 5-HT2A serotonin receptor is an important G protein-coupled receptor that mediates the effects of hallucinogens and the therapeutic actions of a number of commonly prescribed medications, including atypical antipsychotics, antidepressants and anxiolytics. The 5-HT2A receptor, the most abundant serotonin receptor in the cerebral cortex, is enriched in apical dendrites as well as in dendritic spines of pyramidal neurons. A canonical Type I PDZ-binding motif at the carboxyl terminus of the 5-HT2A receptor has been predicted to mediate 5-HT2A receptor interaction with components of the sorting apparatus responsible for establishing neuronal polarity. We discovered that disrupting the PDZ-binding motif on the 5-HT 2A receptor greatly attenuated 5-HT2A receptor targeting to dendrites (without interfering with its axonal exclusion), suggesting that this protein-protein interaction motif is a necessary dendritic targeting signal in cultured cortical pyramidal neurons. Co-immunoprecipitation and immunofluorescent studies subsequently revealed that the PDZ-binding motif mediates the interaction between the 5-HT2A receptor and PSD-95, a prototypic PDZ domain-containing protein and a major regulator of polarized protein sorting in neurons. The association with PSD-95 potentiated 5-HT 2A receptor-mediated signal transduction at least in part by inhibiting the agonist-induced internalization and promoting the cell surface clustering of 5-HT2A receptors in HEK-293 cells. DOI (a 5-HT2 agonist and hallucinogen) and neuronal depolarization promote 5-HT2A receptor trafficking to PSD-95-enriched sites. Additionally, we found that the PDZ-binding motif mediates the neuronal activity-evoked targeting of 5-HT2A receptors to distal dendrites, concomitant with an elevation in 5-HT 2A receptor-mediated signal transduction. Taken together, my studies elucidate a novel role for PDZ-binding domains in the activity-dependent regulation of 5-HT2A receptor signaling and trafficking. These studies will be relevant for understanding how diverse classes of drugs that target the 5-HT2A receptor exert their profound effects on human cognition, emotion and perception.
机译:5-HT 2A 血清素受体是重要的G蛋白偶联受体,介导致幻剂的作用以及许多非处方抗精神病药,抗抑郁药和抗焦虑药的治疗作用。 5-HT 2A 受体是大脑皮层中最丰富的5-羟色胺受体,富含顶突状树突以及锥体神经元的树突棘。预测5-HT 2A 受体羧基末端的典型I型PDZ结合基序可介导5-HT 2A 受体与分选装置组件的相互作用负责建立神经元极性。我们发现破坏5-HT 2A 受体上的PDZ结合基序可以大大减弱5-HT 2A 受体对树突的靶向作用(不影响其轴突排斥),这表明该蛋白-蛋白相互作用基序是培养的皮质锥体神经元中的必需树突状靶向信号。免疫共沉淀和免疫荧光研究随后发现,PDZ结合基序介导了5-HT 2A 受体与PSD-95之间的相互作用,PSD-95是一种具有原型PDZ域的蛋白,是极化蛋白的主要调节剂在神经元中排序。与PSD-95增强的5-HT 2A 受体介导的信号转导的关联至少部分是通过抑制激动剂诱导的内在化并促进5-HT 2A的细胞表面聚集而实现的。 HEK-293细胞中的sub>受体。 DOI(5-HT 2 激动剂和迷幻剂)和神经元去极化促进了5-HT 2A 受体向PSD-95富集位点的转运。此外,我们发现,PDZ结合基序介导了神经元活性引起的5-HT 2A 受体对远端树突的靶向,同时伴随着5-HT 2A 的升高受体介导的信号转导。综上所述,我的研究阐明了PDZ结合域在5-HT 2A 受体信号传导和转运的活性依赖性调节中的新作用。这些研究将有助于理解针对5-HT 2A 受体的多种药物如何对人类的认知,情感和知觉产生深远的影响。

著录项

  • 作者

    Xia, Zongqi.;

  • 作者单位

    Case Western Reserve University (Health Sciences).;

  • 授予单位 Case Western Reserve University (Health Sciences).;
  • 学科 Biology Neuroscience.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 255 p.
  • 总页数 255
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经科学;
  • 关键词

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