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The effect of fluid shear stress in hydrogen sulphide production and cystathionine γ-lyase expression in human early endothelial progenitor cells.
Hu, Qingsong; Zhang, Baojian; Liu, Yulong; Guo, Yiqun; Zhang, Tao; Nie, Ruqiong; Ke, Xiao; Dong, Xiaobian.
Afiliación
  • Hu Q; Department of Cardiology, First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Zhang B; Cardiac Care Unit, Affiliated Hospital of Traditional Chinese Medicine, Xinjiang Medical University, Urumqi, China.
  • Liu Y; Department of Intervention and Vascular Surgery, First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Guo Y; Department of Interventional Radiology and Vascular Anomalies, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Zhang T; Department of Cardiology, First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Nie R; Department of Cardiology, Guangzhou Province Key Laboratory of Arrhymia and Electrophysiology, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou, China.
  • Ke X; Department of Cardiology, Fuwai Hospital, Chinese Academy of Medical Sciences, Shenzhen, China.
  • Dong X; Department of Cardiology, First Affiliated Hospital of Jinan University, Guangzhou, China.
Ann Transl Med ; 8(20): 1318, 2020 Oct.
Article en En | MEDLINE | ID: mdl-33209898
ABSTRACT

BACKGROUND:

Physiological fluid shear stress has been shown to have a beneficial impact on vascular homeostasis. Endothelial progenitor cells (EPCs) make a significant contribution to maintaining endothelial integrity. Therefore, we hypothesised that shear stress-induced endothelium protection plays a role in hydrogen sulphide (H2S) production and up-regulation of cystathionine γ-lyase (CSE) expression in EPCs.

METHODS:

Human EPC-derived CSE activity was detected by colorimetric assay, and H2S production was evaluated by membrane adsorption method. Cell proliferation, migration, and adhesion were assessed by MTT, Transwell, and endothelial cell-mediated adhesion assays, respectively. Real-time polymerase chain reaction (RT-PCR) was carried out to analyse gene expression. Protein expression was analysed by western blot.

RESULTS:

Human EPCs were treated with shear stress levels of 5-25 dyn/cm2 for up to 3 h, and 25 dyn/cm2 for up to 24 h. H2S production and CSE mRNA expression in the EPCs were increased by shear stress in a dose-dependent manner in vitro. Likewise, time-dependent shear stress also significantly enhanced CSE protein expression. Compared to static condition, shear stress improved EPCs proliferation, migration and adhesion capacity. Knockdown of CSE expression by small interfering RNA substantially eliminated the shear stress-induced above functions of human EPCs in vitro.

CONCLUSIONS:

This study gives new insight into the regulatory effect of physiological shear stress on the CSE/H2S system in human EPCs. Our findings may contribute to the development of vascular protective research, although the relevant evidence is admittedly indirect.
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