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DOI 10.1016/j.bbrc.2015.07.115

Медицинская библиотека · Biochemical and biophysical research communications · 2015

Laminar shear flow increases hydrogen sulfide and activates a nitric oxide producing signaling cascade in endothelial cells.

Huang Bin, Chen Chang-Ting, Chen Chi-Shia, Wang Yun-Ming, Hsieh Hsyue-Jen, Wang Danny Ling

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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-γ-lyase (CSE), cystathionine-β-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), ERK(T202/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(S473) 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.

Для цитирования: Huang Bin, Chen Chang-Ting, Chen Chi-Shia, Wang Yun-Ming, Hsieh Hsyue-Jen, Wang Danny Ling. Laminar shear flow increases hydrogen sulfide and activates a nitric oxide producing signaling cascade in endothelial cells.. Biochemical and biophysical research communications. 2015. DOI: 10.1016/j.bbrc.2015.07.115.

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