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首页> 外文期刊>International endodontic journal >The effect of lysophosphatidic acid and Rho-associated kinase patterning on adhesion of dental pulp cells.
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The effect of lysophosphatidic acid and Rho-associated kinase patterning on adhesion of dental pulp cells.

机译:溶血磷脂酸和Rho相关的激酶模式对牙髓细胞粘附的影响。

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AIM: To investigate the effects of lysophosphatidic acid (LPA) and the Rho/Rho-associated kinase (ROCK) pathway on adhesion of dental pulp cells (DPCs). METHODOLOGY: Human DPCs were cultured ex vivo. After treatment of LPA and Y-27632, a specific ROCK inhibitor, changes in focal contacts (FCs) were examined by immunofluorescent staining. Activation of FCs proteins was examined by measuring tyrosine 397 phosphorylation of focal adhesion kinase (FAK) and paxillin using immunoblotting. The data were analysed by Student's t-test. RESULTS: The immunofluorescent staining indicated LPA stimulation induced larger focal adhesion in the cell periphery, compared with the control. Inhibition of ROCK by Y-27632 decreased the formation of FCs markedly, even in the LPA-stimulated cells. LPA also increased the level of tyrosine phosphorylation of paxillin at 30min (P<0.05) and FAK at 5 and 30min (P<0.05). Furthermore, p-paxillin levels declined immediately after Y-27632 treatment and remained low at 5, 30, 60min. Y-27632 also suppressed the effects of LPA on p-paxillin and p-FAK at 5 and 30min (P<0.05). CONCLUSION: LPA activated Rho and then subsequently activated ROCK, suggesting that LPA influences the FCs of DPCs by modulating tyrosine phosphorylation of FAK and paxillin via the Rho/ROCK pathway.
机译:目的:研究溶血磷脂酸(LPA)和Rho / Rho相关激酶(ROCK)途径对牙髓细胞(DPCs)粘附的影响。方法:人DPC体外培养。处理LPA和Y-27632(一种特定的ROCK抑制剂)后,通过免疫荧光染色检查了局部接触(FCs)的变化。通过使用免疫印迹测量粘着斑激酶(FAK)和paxillin的酪氨酸397磷酸化来检查FCs蛋白的激活。数据通过学生t检验进行分析。结果:免疫荧光染色表明,与对照组相比,LPA刺激可引起细胞周围更大的粘着斑粘附。 Y-27632对ROCK的抑制作用甚至在LPA刺激的细胞中也明显减少了FC的形成。 LPA还增加了30分钟时帕西林的酪氨酸磷酸化水平(P <0.05),以及5和30分钟时FAK的酪氨酸磷酸化水平(P <0.05)。此外,p-paxillin水平在Y-27632治疗后立即下降,并在5、30、60分钟时保持较低水平。 Y-27632还可以在5和30分钟时抑制LPA对p-paxillin和p-FAK的作用(P <0.05)。结论:LPA激活Rho,然后激活ROCK,表明LPA通过Rho / ROCK途径调节FAK和Paxillin的酪氨酸磷酸化影响DPC的FC。

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