刺激短暂受体潜在通道TRPM3和TRPM8 增加人体前列腺内氧化酶-2 促进剂活性
Nikolas Brandmeier1, Oliver G Rössler1, Gerald Thiel1
1Department of Medical Biochemistry and Molecular Biology, Medical Faculty, University of Saarland, Campus Homburg, 66421 Homburg, Germany.
暂时的受体潜力3 (TRPM3) 和TRPM8通道调节疼痛和温度感觉. 它们的刺激激活了前列腺素内氧化合成酶-2,将TRP通道与炎症媒介的产生联系起来.
科学领域:
- 分子生物学
- 神经科学
- 细胞信号传输
背景情况:
- 短暂受体潜能 (TRP) 通道,特别是TRPM3和TRPM8,对于热感和疼痛感知至关重要.
- 激活TRP通道会触发细胞内级联,导致转录因子的激活.
研究的目的:
- 通过TRPM3和TRPM8刺激激活的延迟反应基因.
- 研究前列腺素内氧化合成酶-2 (PTGS2) 在TRP通道信号传递中的作用.
主要方法:
- 使用由PTGS2促进体驱动的染色体嵌入的记者基因.
- 用TRPM3激活剂孕醇硫酸和TRPM8激活剂冰激活细胞.
- 使用药理抑制剂和PTGS2促进物的突变分析.
主要成果:
- 刺激TRPM3和TRPM8通道强烈地激活了PTGS2促进体.
- 根据抑制剂研究,激活取决于TRPM3和TRPM8的活性.
- 突变分析发现了一个对PTGS2促进体激活至关重要的cAMP反应元素.
结论:
- 刺激TRPM3和TRPM8通道直接提高PTGS2的表达.
- 这表明TRP通道活性与炎症媒介的合成之间存在新的联系.
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