Title: Laminar shear flow increases hydrogen sulfide and activates a nitric oxide producing signaling cascade in endothelial cells
Authors: Huang, Bin
Chen, Chang-Ting
Chen, Chi-Shia
Wang, Yun-Ming
Hsieh, Hsyue-Jen
Wang, Danny Ling
分子醫學與生物工程研究所
Institute of Molecular Medicine and Bioengineering
Keywords: Shear flow;Hydrogen sulfide;Nitric oxide;3-Mercapto-sulfurtransferase;NBD-SCN;Endothelial cell
Issue Date: 4-Sep-2015
Abstract: Laminar shear flow triggers a signaling cascade that maintains the integrity of endothelial cells (ECs). Hydrogen sulfide (H2S), a new gasotransmitter is regarded as an upstream regulator of nitric oxide (NO). Whether the H2S-generating enzymes are correlated to the enzymes involved in NO production under shear flow conditions remains unclear as yet. In the present study, the cultured ECs were subjected to a constant shear flow (12 dyn/cm(2)) in a parallel flow chamber system. We investigated the expression of three key enzymes for H2S biosynthesis, cystathionine-gamma-Iyase (CSE), cystathionine-beta-synthase (CBS), and 3-mercapto-sulfurtransferase (3-MST). Shear flow markedly increased the level of 3-MST. Shear flow enhanced the production of H2S was determined by NBD-SCN reagent that can bind to cysteine/homocystein. Exogenous treatment of NaHS that can release gaseous H2S, ECs showed an increase of phosphorylation in Akt(S473), ERKT202/Y204 and eNOS(S1177). This indicated that H2S can trigger the NO-production signaling cascade. Silencing of CSE, CBS and 3-MST genes by siRNA separately attenuated the phosphorylation levels of Akt(S423) and eNOS(S1177) under shear flow conditions. The particular mode of shear flow increased H2S production. The interplay between H2S and NO-generating enzymes were discussed in the present study. (C) 2015 Elsevier Inc. All rights reserved.
URI: http://dx.doi.org/10.1016/j.bbrc.2015.07.115
http://hdl.handle.net/11536/128136
ISSN: 0006-291X
DOI: 10.1016/j.bbrc.2015.07.115
Journal: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume: 464
Begin Page: 1254
End Page: 1259
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