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PI3Kgamma 依赖性信号转导在小鼠嗅觉受体神经元中的作用。

PI3Kgamma-dependent signaling in mouse olfactory receptor neurons.

机构信息

Center for Smell and Taste, University of Florida, Gainesville, FL 32610-0127 USA.

出版信息

Chem Senses. 2010 May;35(4):301-8. doi: 10.1093/chemse/bjq020. Epub 2010 Feb 26.

Abstract

Phosphatidylinositol 3-kinase (PI3K)-dependent signaling couples to receptors for many different ligands in diverse cellular systems. Recent findings suggest that PI3K-dependent signaling also mediates inhibition of odorant responses in rat olfactory receptor neurons (ORNs). Here, we present evidence that murine ORNs show PI3K-dependent calcium responses to odorant stimulation, they express 2 G protein-coupled receptor (GPCR)-activated isoforms of PI3K, PI3Kbeta and PI3Kgamma, and they exhibit odorant-induced PI3K activity. These findings support our use of a transgenic mouse model to begin to investigate the mechanisms underlying PI3K-mediated inhibition of odorant responses in mammalian ORNs. Mice deficient in PI3Kgamma, a class IB PI3K that is activated via GPCRs, lack detectable odorant-induced PI3K activity in their olfactory epithelium and their ORNs are less sensitive to PI3K inhibition. We conclude that odorant-dependent PI3K signaling generalizes to the murine olfactory system and that PI3Kgamma plays a role in mediating inhibition of odorant responses in mammalian ORNs.

摘要

磷脂酰肌醇 3-激酶 (PI3K)-依赖性信号转导与许多不同配体在不同的细胞系统中的受体偶联。最近的研究结果表明,PI3K 依赖性信号转导也介导了大鼠嗅觉受体神经元 (ORNs) 中气味反应的抑制。在这里,我们提供的证据表明,鼠 ORNs 对气味刺激表现出 PI3K 依赖性钙反应,它们表达 2 种 G 蛋白偶联受体 (GPCR)-激活的 PI3K 同工型,PI3Kbeta 和 PI3Kgamma,并表现出气味诱导的 PI3K 活性。这些发现支持我们使用转基因小鼠模型来开始研究 PI3K 介导的哺乳动物 ORNs 中气味反应抑制的机制。缺乏 PI3Kgamma(一种通过 GPCR 激活的类 IB PI3K)的小鼠在其嗅上皮和 ORNs 中缺乏可检测到的气味诱导的 PI3K 活性,并且对 PI3K 抑制的敏感性降低。我们得出结论,气味依赖性 PI3K 信号转导普遍存在于小鼠嗅觉系统中,PI3Kgamma 在介导哺乳动物 ORNs 中气味反应的抑制中发挥作用。

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