Muscarinic acetylcholine receptor M3 modulates odorant receptor activity via inhibition of β-arrestin-2 recruitment

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作者
Yue Jiang
Yun Rose Li
Huikai Tian
Minghong Ma
Hiroaki Matsunami
机构
[1] Duke University Medical Center,Department of Molecular Genetics and Microbiology
[2] University Program of Genetics and Genomics,Department of Neuroscience
[3] Duke University,Department of Neurobiology
[4] Medical Scientist Training Program,undefined
[5] University of Pennsylvania Perelman School of Medicine,undefined
[6] Cell and Molecular Biology Graduate Group,undefined
[7] University of Pennsylvania Perelman School of Medicine,undefined
[8] University of Pennsylvania School of Medicine,undefined
[9] Duke Institute for Brain Sciences,undefined
[10] Duke University Medical Center,undefined
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The olfactory system in rodents serves a critical function in social, reproductive and survival behaviours. Processing of chemosensory signals in the brain is dynamically regulated in part by an animal’s physiological state. We previously reported that type 3 muscarinic acetylcholine receptors (M3-Rs) physically interact with odorant receptors (ORs) to promote odour-induced responses in a heterologous expression system. However, it is not known how M3-Rs affect the ability of olfactory sensory neurons (OSNs) to respond to odours. Here, we show that an M3-R antagonist attenuates odour-induced responses in OSNs from wild-type, but not M3-R-null, mice. Using a novel molecular assay, we demonstrate that the activation of M3-Rs inhibits the recruitment of β-arrestin-2 to ORs, resulting in a potentiation of odour-induced responses in OSNs. These results suggest a role for acetylcholine in modulating olfactory processing at the initial stages of signal transduction in the olfactory system.
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