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哺乳动物嗅觉受体神经元中的抑制性气味信号传导。

Inhibitory odorant signaling in Mammalian olfactory receptor neurons.

机构信息

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

出版信息

J Neurophysiol. 2010 Feb;103(2):1114-22. doi: 10.1152/jn.00980.2009. Epub 2009 Dec 23.

Abstract

Odorants inhibit as well as excite olfactory receptor neurons (ORNs) in many species of animals. Cyclic nucleotide-dependent activation of canonical mammalian ORNs is well established but it is still unclear how odorants inhibit these cells. Here we further implicate phosphoinositide-3-kinase (PI3K), an indispensable element of PI signaling in many cellular processes, in olfactory transduction in rodent ORNs. We show that odorants rapidly and transiently activate PI3K in the olfactory cilia and in the olfactory epithelium in vitro. We implicate known G-protein-coupled isoforms of PI3K and show that they modulate not only the magnitude but also the onset kinetics of the electrophysiological response of ORNs to complex odorants. Finally, we show that the ability of a single odorant to inhibit another can be PI3K dependent. Our collective results provide compelling support for the idea that PI3K-dependent signaling mediates inhibitory odorant input to mammalian ORNs and at least in part contributes to the mixture suppression typically seen in the response of ORNs to complex natural odorants.

摘要

气味物质在许多动物物种中既能抑制也能兴奋嗅觉受体神经元(ORNs)。环核苷酸依赖性激活经典的哺乳动物 ORNs 已得到充分证实,但气味物质如何抑制这些细胞仍不清楚。在这里,我们进一步表明,磷脂酰肌醇-3-激酶(PI3K)在许多细胞过程中是 PI 信号的不可或缺的组成部分,在啮齿动物 ORNs 的嗅觉转导中起作用。我们表明,气味物质在体外的嗅觉纤毛和嗅觉上皮中快速且短暂地激活了 PI3K。我们表明,已知的 G 蛋白偶联的 PI3K 同工型不仅调节 ORNs 对复杂气味的电生理反应的幅度,而且还调节其起始动力学。最后,我们表明,一种气味物质抑制另一种气味物质的能力可能依赖于 PI3K。我们的综合结果为 PI3K 依赖性信号转导介导哺乳动物 ORNs 的抑制性气味输入的观点提供了有力的支持,并且至少部分有助于 ORNs 对复杂天然气味的反应中通常观察到的混合物抑制。

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