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Effects of low-intensity pulsed ultrasound on nerve growth factor-induced neurite outgrowth mainly through ERK-CREB pathway in PC12 cells

机译:低强度脉冲超声主要通过PC12细胞中的ERK-CREB途径对神经生长因子诱导的神经突生长的影响

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Nerve growth factor (NGF) therapy has been considered as potential therapeutic approach for the treatment of neural injury and degeneration. However, the high concentration of NGF may exert adverse effects and long period treatment of NGF raises an issue of medical cost. Thus, to investigate combination of NGF therapy with other approach to promote neurite outgrowth is of great interest. Here, we intend to explore the possibility and associated molecular mechanisms of combining NGF and low-intensity pulsed ultrasound stimulation (LIPUS) in promoting neurite outgrowth, which is an essential process in neuronal regeneration. PC12 cells, which will differentiate into neurons upon NGF stimulation as the in vitro model. LIPUS (1MHz) was applied to PC12 cells for 10 min every other day with spatial average intensity 50 mW/cm, 20% duty cycle, 100 Hz pulse repetition frequency, and then incubated with NGF. It is found that LIPUS alone could not significantly induce neurite outgrowth in PC12 cells. However, LIPUS could significantly enhance the neurite length in the presence of NGF. In addition, LIPUS alone could increase the phosphorylation of ERK1/2, Akt and CREB. However, LIPUS combined with NGF could only increase the levels of p-ERK1/2 and p-CREB, but not change the level of p-Akt. Taken together, these results provide important insights that LIPUS synergistically enhances NGF-induced ERK1/2-CREB pathway to promote neurite outgrowth.
机译:神经生长因子(NGF)治疗已被认为是治疗神经损伤和变性的潜在治疗方法。然而,高浓度的NGF可能会产生不利影响,并且NGF的长期治疗提出了医疗费用的问题。因此,研究NGF治疗与促进神经突生长的其他方法的结合是非常有意义的。在这里,我们打算探索神经生长因子和低强度脉冲超声刺激(LIPUS)结合促进神经突生长的可能性和相关的分子机制,神经突生长是神经元再生的重要过程。 PC12细胞,将在NGF刺激下分化为神经元,作为体外模型。将LIPUS(1MHz)每隔一天以空间平均强度50 mW / cm,20%占空比,100 Hz脉冲重复频率应用于PC12细胞10分钟,然后与NGF孵育。发现单独的LIPUS不能显着诱导PC12细胞中的神经突生长。但是,在NGF存在的情况下,LIPUS可以显着增加神经突的长度。此外,仅LIPUS可以增加ERK1 / 2,Akt和CREB的磷酸化。然而,LIPUS联合NGF只能增加p-ERK1 / 2和p-CREB的水平,而不能改变p-Akt的水平。综上所述,这些结果提供了重要的见解,即LIPUS协同增强NGF诱导的ERK1 / 2-CREB途径,促进神经突生长。

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