The study on human umbilical vein endothelial cells (HUVECs) proliferation and the best energy in shock waves treatment

2011 
Purpose To explore how different intensity of ultrasonic shock energy influences the human umbilical vein endothelial cells (HUVECs) proliferation, differentiation and the related cytokines, and to ascertain the best energy of CSWT. Methods The HUVECs cell lines were performed using different levels of energy (0, 0.03, 0.09, 0.18, 0.24 mJ/mm 2 ) shock wave treatment in vitro, Utilising CCK8 colorimetric method to detect HUVECs proliferation, real time PCR, Western blotting and Flow Cytometry were utilised to detect the changes in mRNA and protein of VEGF, IL-8, ICAM-1 before and after CSWT treatment. Results The 0.09 mJ/mm 2 shock energy significantly promoted the HUVECs proliferation (p 2 treatment markedly increased the expression of VEGF, IL-8, ICAM-1 (p 2 group were increased compared with the control group (p 0.05, respectively), 0.18 mJ/mm 2 treatment markedly increased the expression of VEGF (p 0.05, respectively), 0.24 mJ/mm 2 treatment showed no significant increase in the expression of VEGF, IL-8, ICAM-1(p>0.05, respectively) compared with the non-treated control. Western blot analysis and Flow Cytometry showed that the expression of VEGF, IL-8, ICAM-1 in 0.09 mJ/mm 2 group were significantly higher than the control group (p 2 group was significantly higher than the control group (p 0.05, respectively); the expression of VEGF in 0.18, 0.24 mJ/mm 2 group was significantly higher than the control group (p 0.05, respectively). Conclusions (1) The different extracorporeal shock wave energy promoted the HUVECs proliferations to different extent, the effect of 0.09 mJ/mm 2 energy is the most evident. (2) The 0.09 mJ/mm 2 energy increase the expression of IL-8, ICAM-1 mRNA and protein most significantly. (3) The 0.09 mJ/mm 2 energy increased the expression of VEGF mRNA and protein most remarkably. (4) The 0.03∼0.24 mJ/mm 2 energies also have some effects in facilitating the secretion of VEGF, IL-8 and ICAM-1.
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