Author
Listed:
- Yue Jiang
(Duke University Medical Center
University Program of Genetics and Genomics, Duke University)
- Yun Rose Li
(Medical Scientist Training Program, University of Pennsylvania Perelman School of Medicine
Cell and Molecular Biology Graduate Group, University of Pennsylvania Perelman School of Medicine)
- Huikai Tian
(University of Pennsylvania School of Medicine)
- Minghong Ma
(Cell and Molecular Biology Graduate Group, University of Pennsylvania Perelman School of Medicine
University of Pennsylvania School of Medicine)
- Hiroaki Matsunami
(Duke University Medical Center
Duke Institute for Brain Sciences, Duke University Medical Center)
Abstract
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.
Suggested Citation
Yue Jiang & Yun Rose Li & Huikai Tian & Minghong Ma & Hiroaki Matsunami, 2015.
"Muscarinic acetylcholine receptor M3 modulates odorant receptor activity via inhibition of β-arrestin-2 recruitment,"
Nature Communications, Nature, vol. 6(1), pages 1-15, May.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7448
DOI: 10.1038/ncomms7448
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