MrgprC11 expression and function in vagal afferent nerves in the esophagus

Xiaoyun Yu1, Yongming Huang1, Mayur J Patil1

  • 1Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.

Insights

Mas1-related G protein-coupled receptor C11 (MrgprC11) activates and sensitizes esophageal vagal afferent C-fibers, offering a new target for treating esophageal pain and heartburn.

Area of Science:

  • Neuroscience
  • Gastroenterology
  • Pain Research

Background:

  • Esophageal pain and heartburn arise from noxious stimulation, but mechanisms are unclear.
  • Mas1-related G protein-coupled receptors (Mrgprs) mediate somatic pain and itch.
  • The role of MrgprC11 in esophageal nociception is unknown.

Purpose of the Study:

  • To investigate the functional expression and role of MrgprC11 in esophageal afferent neurons.
  • To determine if MrgprC11 mediates esophageal nociception.

Main Methods:

  • RT-PCR to assess MrgprC11 mRNA expression in esophagus, DRG, and vagal ganglia.
  • Confocal imaging to visualize MrgprC11-positive nerve fibers in esophageal tissues.
  • Two-photon imaging and extracellular recordings to evaluate functional responses to MrgprC11 agonist BAM8-22 in vagal neurons and esophageal C-fibers.
  • Comparison between wild-type and Mrgpr-cluster knockout mice.

Main Results:

  • MrgprC11 mRNA was found in DRG and vagal ganglia, with positive nerve fibers abundant in the esophageal wall.
  • The MrgprC11 agonist BAM8-22 increased calcium influx in vagal afferent neurons.
  • BAM8-22 evoked action potentials in wild-type but not knockout mouse esophageal vagal C-fibers.
  • Esophageal distension-induced responses were enhanced by BAM8-22 in wild-type but not knockout mice.

Conclusions:

  • MrgprC11 is functionally expressed in esophageal vagal afferent C-fibers.
  • MrgprC11 activation leads to sensitization of these fibers.
  • MrgprC11 represents a novel mechanism and potential therapeutic target for esophageal nociception.

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