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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Functional expression of corticotropin-releasing hormone (CRH) receptor 1 in cultured rat microglia.
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Functional expression of corticotropin-releasing hormone (CRH) receptor 1 in cultured rat microglia.

机译:促肾上腺皮质激素释放激素(CRH)受体1在培养的大鼠小胶质细胞中的功能性表达。

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摘要

Corticotropin-releasing hormone (CRH), known as a key regulator of the hypothalamic-pituitary-adrenal axis response to stress, elicits its biological effects by binding to two membrane receptors (CRH-R1 and CRH-R2). The present studies examined the presence of functional expression of CRH receptors in cultured microglia of rat. CRH-R1 mRNA and protein were detected by reverse transcriptase polymerase chain reaction (RT-PCR), western blotting and receptor chemical cross-linking assay in cultured microglia. CRH-R2 mRNA was undetectable by RT-PCR. The radioligand binding analysis using [125I]Tyr-rat/human CRH revealed a high affinity binding site (Kd of 1.2 nm and Bmax of 84 fmol/mg of protein). Competition studies using CRH and related peptides indicated kinetic and pharmacological characteristics consistent with the CRH-R1 receptor subtype. Receptor chemical cross-linking assay demonstrated a single band of CRH receptor with a molecular weight of -77 kDa, which was inhibited in the presence of excess unlabeled rat/human CRH in a dose-dependent manner and inhibited by a CRH receptor antagonist astressin. Functional coupled cAMP production in cultured microglia was stimulated by exogenous addition of CRH and related peptides in a dose-dependent manner and blocked by astressin. Our findings suggest the functional expression of CRH-R1 receptor in rat microglia, indicating an important mechanism of interaction between immune and neuroendocrine systems in brain physiological and pathological conditions.
机译:促肾上腺皮质激素释放激素(CRH)是下丘脑-垂体-肾上腺轴对压力反应的关键调节因子,它通过与两个膜受体(CRH-R1和CRH-R2)结合而引起生物学效应。本研究检查了培养的大鼠小胶质细胞中CRH受体功能表达的存在。通过逆转录聚合酶链反应(RT-PCR),蛋白质印迹法和受体化学交联法检测培养的小胶质细胞中CRH-R1的mRNA和蛋白。 RT-PCR检测不到CRH-R2 mRNA。使用[125I] Tyr-rat /人CRH进行的放射性配体结合分析显示出高亲和力结合位点(Kd为1.2 nm,Bmax为84 fmol / mg蛋白质)。使用CRH和相关肽的竞争研究表明动力学和药理学特征与CRH-R1受体亚型一致。受体化学交联测定法证明了一条分子量为-77 kDa的CRH受体单条带,该条带在过量未标记大鼠/人CRH的存在下以剂量依赖性方式被抑制,并被CRH受体拮抗剂astressin抑制。通过外源添加CRH和相关肽以剂量依赖性方式刺激培养的小胶质细胞中功能性偶联cAMP的产生,并被astressin阻断。我们的发现表明CRH-R1受体在大鼠小胶质细胞中的功能表达,表明在大脑生理和病理状况下免疫系统和神经内分泌系统之间相互作用的重要机制。

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