首页> 美国卫生研究院文献>American Journal of Physiology - Gastrointestinal and Liver Physiology >The expression profile of acid-sensing ion channel (ASIC) subunits ASIC1a ASIC1b ASIC2a ASIC2b and ASIC3 in the esophageal vagal afferent nerve subtypes
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The expression profile of acid-sensing ion channel (ASIC) subunits ASIC1a ASIC1b ASIC2a ASIC2b and ASIC3 in the esophageal vagal afferent nerve subtypes

机译:酸敏感离子通道(ASIC)亚基ASIC1aASIC1bASIC2aASIC2b和ASIC3在食管迷走神经传入神经亚型中的表达谱

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摘要

Acid-sensing ion channels (ASICs) have been implicated in esophageal acid sensing and mechanotransduction. However, insufficient knowledge of ASIC subunit expression profile in esophageal afferent nerves hampers the understanding of their role. This knowledge is essential because ASIC subunits form heteromultimeric channels with distinct functional properties. We hypothesized that the esophageal putative nociceptive C-fiber nerves (transient receptor potential vanilloid 1, TRPV1-positive) express multiple ASIC subunits and that the ASIC expression profile differs between the nodose TRPV1-positive subtype developmentally derived from placodes and the jugular TRPV1-positive subtype derived from neural crest. We performed single cell RT-PCR on the vagal afferent neurons retrogradely labeled from the esophagus. In the guinea pig, nearly all (90%–95%) nodose and jugular esophageal TRPV1-positive neurons expressed ASICs, most often in a combination (65–75%). ASIC1, ASIC2, and ASIC3 were expressed in 65–75%, 55–70%, and 70%, respectively, of both nodose and jugular TRPV1-positive neurons. The ASIC1 splice variants ASIC1a and ASIC1b and the ASIC2 splice variant ASIC2b were similarly expressed in both nodose and jugular TRPV1-positive neurons. However, ASIC2a was found exclusively in the nodose neurons. In contrast to guinea pig, ASIC3 was almost absent from the mouse vagal esophageal TRPV1-positive neurons. However, ASIC3 was similarly expressed in the nonnociceptive TRPV1-negative (tension mechanoreceptors) neurons in both species. We conclude that the majority of esophageal vagal nociceptive neurons express multiple ASIC subunits. The placode-derived nodose neurons selectively express ASIC2a, known to substantially reduce acid sensitivity of ASIC heteromultimers. ASIC3 is expressed in the guinea pig but not in the mouse vagal esophageal TRPV1-positive neurons, indicating species differences in ASIC expression.
机译:酸感应离子通道(ASICs)与食道酸感应和机械转导有关。但是,对食管传入神经中的ASIC亚基表达谱的了解不足,妨碍了对其作用的理解。该知识必不可少,因为ASIC亚基形成具有不同功能特性的异多聚体通道。我们假设食管推定的伤害性C纤维神经(瞬时受体电位香草样1,TRPV1阳性)表达多个ASIC亚基,并且从斑块发展而来的结节TRPV1阳性亚型与颈静脉TRPV1阳性之间的ASIC表达谱不同亚型源自神经c。我们对从食管逆行标记的迷走神经传入神经元进行了单细胞RT-PCR。在豚鼠中,几乎所有(90%–95%)结节和食管TRPV1阳性神经元均表达ASIC,多数情况下是组合使用(65-75%)。结节和颈TRPV1阳性神经元的ASIC1,ASIC2和ASIC3分别表达为65-75%,55-70%和70%。 ASIC1剪接变体ASIC1a和ASIC1b以及ASIC2剪接变体ASIC2b在结节和颈TRPV1阳性神经元中均类似表达。但是,ASIC2a仅在结节神经元中发现。与豚鼠相反,小鼠迷路食道TRPV1阳性神经元几乎没有ASIC3。但是,ASIC3在两个物种的非伤害性TRPV1阴性(张力机械感受器)神经元中表达相似。我们得出的结论是,大多数食管迷走神经感受伤害性神经元表达多个ASIC亚基。源自placode的结节神经元选择性表达ASIC2a,已知该ASIC2a会大大降低ASIC异源多聚体的酸敏感性。 ASIC3在豚鼠中表达,但在小鼠迷路食道TRPV1阳性神经元中不表达,表明ASIC表达中存在种种差异。

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