IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v6y2015i1d10.1038_ncomms7448.html
   My bibliography  Save this article

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

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
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms7448
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms7448?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7448. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.