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Dynamic activation of Src induced by low-power laser irradiation in living cells mediated by reactive oxygen species

机译:由活性氧物质介导的活细胞低功率激光辐射诱导SRC的动态激活

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Low-power laser irradiation (LPLI) leads to photochemical reaction and then activates intracellular several signaling pathway. Reactive oxygen species (ROS) are considered to be the primary messengers produced by LPLI. Here, we studied the signaling pathway mediated by ROS upon the stimulation of LPLI. Src tyrosine kinases are well-known targets of ROS and can be activated by oxidative events. Using a Src reporter based on fluorescence resonance energy transfer (FRET) technique, we visualized the dynamic Src activation in Hela cells immediately after LPLI. Moreover, Src activity was enhanced by increasing the duration of LPLI. In addition, our results suggested that ROS were key mediators of Src activation, as ROS scavenger, vitamin C decreased and exogenous H_2O_2 increased the activity of Src. Meanwhile, Goe6983 loading did not block the effect of LPLI. CCK-8 experiments proved that cell vitality was prominently improved by LPLI with all the doses we applied in our experiments ranging from 3 to 25J/cm~2. The results indicated that LPLI/ROS/Src pathway may be involved in the LPLI biostimulation effects.
机译:低功率激光辐射(LPLI)导致光化学反应,然后激活细胞内几种信号通路。反应性氧物种(ROS)被认为是LPLI生产的主要信使。在这里,我们研究了在刺激LPLI时由ROS介导的信号通路。 SRC酪氨酸激酶是ROS的众所周知的靶标,可以通过氧化事件激活。使用基于荧光共振能量转移(FRET)技术的SRC报道器,在LPLI之后立即可视化HELA细胞的动态SRC激活。此外,通过增加LPLI的持续时间来提高SRC活性。此外,我们的结果表明ROS是SRC活化的关键介质,作为ROS清除剂,维生素C降低,外源H_2O_2增加了SRC的活性。同时,GOE6983装载没有阻断LPLI的效果。 CCK-8实验证明,LPLI突出地改善了细胞活力,我们在我们的实验中施用的所有剂量范围为3至25J / cm〜2。结果表明,LPLI / ROS / SRC途径可以参与LPLI生物抑制效应。

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