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Detection of G Protein-coupled Receptor Expression in Mouse Vagal Afferent Neurons using Multiplex In Situ Hybridization
Published on: September 20, 2021
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.
Abstract:
Noxious stimulation-induced esophageal nociception plays a crucial role in generating esophageal pain and heartburn, but the underlying mechanism remains unclear. MrgprC11 is a recently discovered member belonging to Mas1-related G protein-coupled receptor (Mrgpr) family, which is selectively expressed in afferent DRG neurons and distinctively encodes somatic pain and itch sensations. Whether MrgprC11 is also functionally expressed in esophageal afferent neurons and mediates esophageal nociception has yet to be defined. We first compared MrgprC11 mRNA expressions in the esophagus, DRG, and vagal ganglia by RT-PCR. MrgprC11-positive nerve fiber distributions were revealed by confocal imaging in the whole mount esophageal tissues using the MrgprC11tdTomato mouse. We then addressed the MrgprC11 agonist bovine adrenal medulla peptide 8-22 (BAM8-22)-evoked functional responses in vagal afferent neurons by two-photon imaging using pirt-GCaMP6 mice and in esophageal vagal C-fibers by extracellular recording from wild-type and Mrgpr-clusterΔ-/- mice. MrgprC11 mRNA expression was identified in the DRG and vagal ganglia, but not the esophagus. MrgprC11-positive nerve fibers were richly distributed in the wall of the esophagus. MrgprC11 agonist BAM8-22 elicited a significant increase in calcium influx in vagal afferent neurons. When applied to the esophageal vagal C-fiber nerve terminals in extracellular recordings, BAM8-22-evoked action potential discharges in the C-fibers only in wild-type but not in Mrgpr-clusterΔ-/- mice. Following activation, esophageal distension-induced action potential discharges were significantly enhanced in wild-type but not in knockout animals. The present study demonstrated a functional role of MrgprC11 in mediating activation and sensitization of esophageal vagal afferent C-fibers, revealing a new mechanism and potential target for esophageal nociception.NEW & NOTEWORTHY MrgprC11 belongs to the recently discovered Mrgpr family and plays a crucial role in somatic sensory transduction. Its functional expression in visceral esophageal afferent nerves has yet to be defined. The present study demonstrated a functional role of MrgprC11 in mediating activation and sensitization of esophageal vagal afferent C-fibers, revealing a novel nociceptive sensory transduction mechanism in the esophagus.
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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