Oncotarget

Research Papers:

Sulfhydration-associated phosphodiesterase 5A dimerization mediates vasorelaxant effect of hydrogen sulfide

Yan Sun, Yaqian Huang, Wen Yu, Siyao Chen, Qiuyu Yao, Chunyu Zhang, Dingfang Bu, Chaoshu Tang, Junbao Du and Hongfang Jin _

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Oncotarget. 2017; 8:31888-31900. https://doi.org/10.18632/oncotarget.16649

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Abstract

Yan Sun1,*, Yaqian Huang1,*, Wen Yu1,*, Siyao Chen2, Qiuyu Yao1, Chunyu Zhang1, Dingfang Bu3, Chaoshu Tang4, Junbao Du1,5, Hongfang Jin1

1Department of Pediatrics, Peking University First Hospital, Beijing, 100034, China

2Department of Cardiac Surgery, Guangdong General Hospital, Guangzhou, 510000, China

3Centre Laboratory of Peking University First Hospital, Beijing, 100034, China

4Department of Physiology and Pathophysiology, Peking University Health Science Center, Beijing, 100034, China

5Key Laboratory of Cardiovascular Sciences, Ministry of Education, Beijing, 100034, China

*These authors contributed equally to this work

Correspondence to:

Hongfang Jin, email: jinhongfang51@126.com

Keywords: hydrogen sulfide, sGC/PDE/cGMP/PKG, dimer, sulfhydrylation

Received: August 20, 2016     Accepted: March 16, 2017     Published: March 29, 2017

ABSTRACT

The study was designed to examine if the vasorelaxant effect of hydrogen sulfide was mediated by sulfhydration-associated phosphodiesterase (PDE) 5A dimerization. The thoracic aorta of rat was separated and the vasorelaxant effects were examined with in vitro vascular perfusion experiments. The dimerization and sulfhydration of PDE 5A and soluble guanylatecyclase (sGC) were measured. PDE 5A and protein kinase G (PKG) activities were tested. Intracellular cGMP content was detected by enzyme-linked immunosorbent assay (ELISA). The results showed that NaHS relaxed isolated rat vessel rings at an EC50 of (1.79 ± 0.31)×10−5mol/L, associated with significantly increased PKG activity and cGMP content in vascular tissues. Sulfhydration of sGC β1 was increased, while the levels of sGC αβ1 dimers were apparently decreased after incubation with NaHS in vascular tissues. Moreover, PDE 5A homodimers were markedly decreased, and accordingly the PDE 5A activity demonstrated by the content of 5′-GMP was significantly decreased after incubation with NaHS or GYY4137. Mechanistically, both NaHS and GYY4137 significantly enhanced the PDE 5A sulfhydration in vascular tissues. DTT partially abolished the effects of NaHS on PDE 5A activity, cGMP content and vasorelaxation. Therefore, the present study for the first time suggested that H2S exerted vasorelaxant effect probably via sulfhydration-associated PDE 5A dimerization.


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