The gasotransmitter hydrogen sulfide inhibits transepithelial anion secretion of pregnant mouse endometrial epithelium

• Published in: Nitric oxide 2019-09, Vol.90, p.37-46
• Main Authors: Xu, Jia-Wen, Gao, Dong-Dong, Peng, Lei, Qiu, Zhuo-Er, Ke, Li-Jiao, Zhu, Yun-Xin, Zhang, Yi-Lin, Zhou, Wen-Liang
• Format: Article
• Language: English
• Subjects: Animals; Anion secretion; Anions - antagonists & inhibitors; Anions - metabolism; Biological Transport - drug effects; CFTR; Embryo implantation; Endometrial epithelium; Endometrium - drug effects; Endometrium - metabolism; Epithelial Cells - drug effects; Epithelial Cells - metabolism; Female; Gasotransmitters - pharmacology; H2S; Hydrogen Sulfide - pharmacology; Ion transport; Mice; Mice, Inbred Strains; Pregnancy
• ISSN: 1089-8603; 1089-8611; 1089-8611
• DOI: 10.1016/j.niox.2019.05.011

Endometrial epithelium exhibits a robust ion transport activity required for dynamical regulation of uterine fluid environment and thus embryo implantation. However, there still lacks a thorough understanding of the ion transport processes and regulatory mechanism in peri-implantation endometrial epithelium. As a gaseous signaling molecule or gasotransmitter, hydrogen sulfide (H2S) regulates a myriad of cellular and physiological processes in various tissues, including the modulation of ion transport proteins in epithelium. This study aimed to investigate the effects of H2S on ion transport across mouse endometrial epithelium and its possible role in embryo implantation. The existence of endogenous H2S in pregnant mouse uterus was tested by the detection of two key H2S-generating enzymes and measurement of H2S production rate in tissue homogenates. Transepithelial ion transport processes were electrophysiologically assessed in Ussing chambers on early pregnant mouse endometrial epithelial layers, demonstrating that H2S suppressed the anion secretion by blocking cystic fibrosis transmembrane conductance regulator (CFTR). H2S increased intracellular Cl− concentration ([Cl−]i) in mouse endometrial epithelial cells, which was abolished by pretreatment with the CFTR selective inhibitor CFTRinh-172. The cAMP level in mouse endometrial epithelial cells was not affected by H2S, indicating that H2S blocked CFTR in a cAMP-independent way. In vivo study showed that interference with H2S synthesis impaired embryo implantation. In conclusion, our study demonstrated that H2S inhibits the transepithelial anion secretion of early pregnant mouse endometrial epithelium via blockade of CFTR, contributing to the preparation for embryo implantation. •The expression and activity of CBS/CTH exhibited an increasing tendency in mouse uterus during early pregnancy.•H2S decreased ISC in pregnant mouse endometrial epithelium via inhibition of CFTR.•H2S increased [Cl−]i of mouse endometrial epithelial cells by blockade of CFTR.•Interference with H2S synthesis in vivo partially impaired embryo implantation.