MrgprC11 expression and function in vagal afferent nerves in the esophagus.

IF 3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Xiaoyun Yu, Yongming Huang, Mayur J Patil, Yanyan Xing, Fei Ru, Ryo Kawamoto, Liang Han, Bradley J Undem, Xinzhong Dong, Shaoyong Yu
{"title":"MrgprC11 expression and function in vagal afferent nerves in the esophagus.","authors":"Xiaoyun Yu, Yongming Huang, Mayur J Patil, Yanyan Xing, Fei Ru, Ryo Kawamoto, Liang Han, Bradley J Undem, Xinzhong Dong, Shaoyong Yu","doi":"10.1152/ajpgi.00363.2025","DOIUrl":null,"url":null,"abstract":"<p><p>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 MrgprC11<sup>tdTomato</sup> 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 <i>Mrgpr-clusterΔ</i><sup>-/-</sup> 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 <i>Mrgpr-clusterΔ</i><sup>-/-</sup> 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.<b>NEW & NOTEWORTHY</b> 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.</p>","PeriodicalId":7725,"journal":{"name":"American journal of physiology. Gastrointestinal and liver physiology","volume":" ","pages":"G341-G348"},"PeriodicalIF":3.0000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13403071/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Gastrointestinal and liver physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpgi.00363.2025","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/11 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

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.

MrgprC11在食道迷走传入神经中的表达及功能。
有害刺激引起的食道痛觉在食道疼痛和胃灼热中起着至关重要的作用,但其潜在机制尚不清楚。MrgprC11是最近发现的mas1相关G蛋白偶联受体(Mrgpr)家族成员,它在传入DRG神经元中选择性表达,并独特地编码躯体疼痛和瘙痒感觉。MrgprC11是否也在食道传入神经元中功能性表达并介导食道伤害感受尚不明确。我们首先通过RT-PCR比较了MrgprC11 mRNA在食道、DRG和迷走神经节中的表达。MrgprC11tdTomato小鼠全贴装食管组织共聚焦成像显示mrgprc11阳性神经纤维分布。然后,我们利用prt - gcamp6小鼠的双光子成像和野生型和Mrgpr-cluster-/-小鼠的细胞外记录,研究了MrgprC11激动剂BAM8-22在迷走神经传入神经元中引起的功能反应。MrgprC11 mRNA在DRG和迷走神经节中表达,而在食道中未表达。mrgprc11阳性神经纤维丰富分布于食管壁。MrgprC11激动剂BAM8-22引起迷走神经传入神经元钙内流的显著增加。当将BAM8-22应用于细胞外记录的食道迷走c -纤维神经末梢时,BAM8-22仅在野生型小鼠中引起c -纤维的动作电位放电,而在mrpr -cluster-/-小鼠中没有引起动作电位放电。激活后,食管扩张引起的动作电位放电在野生型而非敲除型动物中显著增强。本研究证实了MrgprC11在介导食道迷走神经传入c纤维的激活和致敏中的功能作用,揭示了食道伤害感觉的新机制和潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.40
自引率
2.20%
发文量
104
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Gastrointestinal and Liver Physiology publishes original articles pertaining to all aspects of research involving normal or abnormal function of the gastrointestinal tract, hepatobiliary system, and pancreas. Authors are encouraged to submit manuscripts dealing with growth and development, digestion, secretion, absorption, metabolism, and motility relative to these organs, as well as research reports dealing with immune and inflammatory processes and with neural, endocrine, and circulatory control mechanisms that affect these organs.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书