Department of Pharmaceutical Physiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, 930-0194, Japan.
Department of Pharmaceutical Physiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, 930-0194, Japan.
Biochem Biophys Res Commun. 2019 Oct 20;518(3):605-609. doi: 10.1016/j.bbrc.2019.08.099. Epub 2019 Aug 21.
In the stomach, Sonic Hedgehog (Shh) is highly expressed in gastric parietal cells, and acts as a morphogen in early development of the organ. Here, we found that the cleaved N-terminal fragment of Shh (Shh-N) was abundantly expressed in hog gastric vesicles derived from the apical membrane of parietal cells. Interestingly, Shh-N recombinant significantly decreased K-dependent ATP-hydrolyzing activity, which is sensitive to an inhibitor of H,K-ATPase (SCH28080), in hog gastric tubulovesicles and membrane fractions of the H,K-ATPase-expressing cells. In the living cells, Shh-N recombinant inhibited the SCH28080-sensitive Rb-uptake. Together, Shh-N may directly bind to extracellular side of H,K-ATPase, and negatively regulates the pump activity. This is the first report to explore non-morphogenic property of Shh on ion transporters.
在胃中,Sonic Hedgehog(Shh)在胃壁细胞中高度表达,并在器官的早期发育中充当形态发生素。在这里,我们发现 Shh 的裂解 N 端片段(Shh-N)在源自壁细胞顶膜的猪胃小泡中大量表达。有趣的是,Shh-N 重组蛋白显著降低了 hog 胃微管泡和表达 H,K-ATPase 细胞的膜部分中对 H,K-ATPase 抑制剂(SCH28080)敏感的 K 依赖性 ATP 水解活性。在活细胞中,Shh-N 重组蛋白抑制了对 SCH28080 敏感的 Rb 摄取。总之,Shh-N 可能直接结合到 H,K-ATPase 的细胞外侧面,并负调控泵的活性。这是首次探索 Shh 对离子转运体的非形态发生特性。