Dusenkova Svetlana, Ru Fei, Surdenikova Lenka, Nassenstein Christina, Hatok Jozef, Dusenka Robert, Banovcin Peter, Kliment Jan, Tatar Milos, Kollarik Marian
Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Pathophysiology, Comenius University in Bratislava, Jessenius Faculty of Medicine, Martin, Slovakia;
Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland;
Am J Physiol Gastrointest Liver Physiol. 2014 Nov 1;307(9):G922-30. doi: 10.1152/ajpgi.00129.2014. Epub 2014 Sep 4.
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.
酸敏感离子通道(ASICs)与食管酸感受和机械转导有关。然而,对食管传入神经中ASIC亚基表达谱的了解不足阻碍了对其作用的理解。这一知识至关重要,因为ASIC亚基形成具有不同功能特性的异源多聚体通道。我们假设食管假定的伤害性C纤维神经(瞬时受体电位香草酸亚型1,TRPV1阳性)表达多种ASIC亚基,并且在发育上源自基板的结节TRPV1阳性亚型和源自神经嵴的颈静脉TRPV1阳性亚型之间,ASIC表达谱有所不同。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逆转录聚合酶链反应。在豚鼠中,几乎所有(90%-95%)的结节和颈静脉食管TRPV1阳性神经元都表达ASICs,大多数情况下是组合表达(65%-75%)。ASIC1、ASIC2和ASIC3分别在65%-75%、55%-70%和70%的结节和颈静脉TRPV1阳性神经元中表达。ASIC1剪接变体ASIC1a和ASIC1b以及ASIC2剪接变体ASIC2b在结节和颈静脉TRPV1阳性神经元中表达相似。然而,ASIC2a仅在结节神经元中发现。与豚鼠不同,小鼠迷走神经食管TRPV1阳性神经元中几乎没有ASIC3。然而,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。我们得出结论,大多数食管迷走神经伤害性神经元表达多种ASIC亚基。源自基板的结节神经元选择性表达ASIC2a,已知其可显著降低ASIC异源多聚体的酸敏感性。ASIC3在豚鼠的迷走神经食管TRPV1阳性神经元中表达,但在小鼠中不表达,表明ASIC表达存在物种差异。