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III型腺苷酸环化酶基因的破坏导致转基因小鼠出现外周性和行为性嗅觉缺失。

Disruption of the type III adenylyl cyclase gene leads to peripheral and behavioral anosmia in transgenic mice.

作者信息

Wong S T, Trinh K, Hacker B, Chan G C, Lowe G, Gaggar A, Xia Z, Gold G H, Storm D R

机构信息

Department of Pharmacology, University of Washington, Seattle 98195, USA.

出版信息

Neuron. 2000 Sep;27(3):487-97. doi: 10.1016/s0896-6273(00)00060-x.

Abstract

Cyclic nucleotide-gated ion channels in olfactory sensory neurons (OSNs) are hypothesized to play a critical role in olfaction. However, it has not been demonstrated that the cAMP signaling is required for olfactory-based behavioral responses, and the contributions of specific adenylyl cyclases to olfaction have not been defined. Here, we report the presence of adenylyl cyclases 2, 3, and 4 in olfactory cilia. To evaluate the role of AC3 in olfactory responses, we disrupted the gene for AC3 in mice. Interestingly, electroolfactogram (EOG) responses stimulated by either cAMP- or inositol 1,4,5-triphosphate- (IP3-) inducing odorants were completely ablated in AC3 mutants, despite the presence of AC2 and AC4 in olfactory cilia. Furthermore, AC3 mutants failed several olfaction-based behavioral tests, indicating that AC3 and cAMP signaling are critical for olfactory-dependent behavior.

摘要

嗅觉感觉神经元(OSNs)中的环核苷酸门控离子通道被认为在嗅觉中起关键作用。然而,尚未证实基于嗅觉的行为反应需要cAMP信号传导,并且特定腺苷酸环化酶对嗅觉的贡献尚未明确。在这里,我们报告在嗅觉纤毛中存在腺苷酸环化酶2、3和4。为了评估AC3在嗅觉反应中的作用,我们破坏了小鼠中的AC3基因。有趣的是,尽管嗅觉纤毛中存在AC2和AC4,但在AC3突变体中,由cAMP或肌醇1,4,5-三磷酸(IP3)诱导的气味剂刺激引起的嗅觉电图(EOG)反应完全消失。此外,AC3突变体在几项基于嗅觉的行为测试中失败,表明AC3和cAMP信号传导对嗅觉依赖性行为至关重要。

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