[Netrin-1对T-ALL细胞VEGFA表达的影响及其机制]。

Yao Zhu, Hai-Yan Liu, Yan Xiang, Hui Yang, Xin-Yuan Yao, Xi-Zhou An, Kai-Nan Zhang, Lan Huang, Shao-Yan Liang, Jie Yu
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引用次数: 0

摘要

摘要目的:探讨轴突引导因子Netrin-1对T细胞急性淋巴细胞白血病(T- all)中VEGFA表达的影响及其相关机制。方法:采用ELISA法检测T-ALL患儿骨髓(BM)中Netrin-1和VEGFA的水平。比较对照组患儿与患者Netrin-1、VEGFA水平,并分析Netrin-1与VEGFA的线性相关性。体外培养T-ALL细胞Jurkat和Molt-4,分别用不同浓度的Netrin-1(0、25、50、100 ng/ml)处理细胞24 h,采用定量RT-PCR (qRT-PCR)和Western blot检测Jurkat、Molt-4细胞中VEGFA的表达。采用qRT-PCR检测T-ALL细胞中Netrin-1受体的表达,采用co-IP检测各细胞中Netrin-1与受体的相互作用。采用Western blot检测Netrin-1 (100 ng/ml)处理T-ALL细胞后AKT信号转导通路关键蛋白AKT、mTOR的磷酸化水平。用Netrin-1 (100 ng/ml)联合AKT或mTOR特异性抑制剂处理T-ALL细胞后,Western blot检测VEGFA的表达和AKT通路转导器的磷酸化水平。结果:T-ALL患者BM标本中Netrin-1和VEGFA的表达水平均显著高于对照组。Netrin-1的表达水平与VEGFA的表达水平呈正相关(r2=0 ~ 974)。随着Netrin-1浓度的升高,VEGFA的表达水平也随之升高(结论:T-ALL患儿骨髓中Netrin-1和VEGFA表达异常,且两者之间存在线性关系。Netrin-1可与其受体整合素-β4相互作用,激活AKT转导通路,提高T-ALL细胞中VEGFA的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effect of Netrin-1 on VEGFA Expression in T-ALL Cells and Its Related Mechanism].

AbstractObjective: To investigate the effect of the axon guidance factor Netrin-1 on the expression of VEGFA in T cell acute lymphoblastic leukemia(T-ALL) and its related mechanism.

Methods: ELISA assays were applied to detect the levels of Netrin-1 and VEGFA in the bone marrow (BM) samples from children in the T-ALL and control group. The level of Netrin-1 and VEGFA were compared between control children and patients, and the liner correlation between Netrin-1 and VEGFA was analyzed. The T-ALL cells Jurkat and Molt-4 were culture in vitro, and the cells were treated with different concentration of Netrin-1 (0, 25, 50, 100 ng/ml) for 24 h, quantitative RT-PCR (qRT-PCR) and Western blot were used to detect the VEGFA expression in Jurkat, Molt-4 cells. The expression of Netrin-1 receptors in T-ALL cells was detected by qRT-PCR and the interaction between Netrin-1 and receptor in each cells was detected by co-IP. Furthermore, Western blot was used to detect the phosphorylation level of key prateins of AKT signal transduction pathway including Akt and mTOR in T-ALL cells treated with Netrin-1 (100 ng/ml). The expression of VEGFA and phosphorylation of AKT pathway transducers were detected by Western blot, after T-ALL cells treated with Netrin-1 (100 ng/ml) combined with inhibitors specific to Akt or mTOR.

Results: The expression level of Netrin-1 and VEGFA in T-ALL patients BM samples were both signi-ficantly higher than that of control group. And the expression level of Netrin-1 was positively correlated with that of VEGFA(r2=0974). With the increase of Netrin-1 concentration, the expression level of VEGFA also increased(P<0.05). Netrin-1 interacted with its receptor, integrin-β4 at the Netrin-1 concentration of 100 ng/ml. Further, the treatment of Netrin-1 could increase the phosphorylation of Akt and mTOR, which were the key transducers of AKT pathway. After treatment of T-ALL cells with Netrin-1 (100 ng/mL) and Akt inhibitor, the expression of VEGFA and phosphorylation of Akt or mTOR decreased. When the cells were treated with Netrin-1(100 ng/ml) and mTOR inbititor, the phosphorylation level of mTOR and the expression of VEGFA decreased, the phosphorylation level of Akt increased.

Conclusion: The expression of Netrin-1 and VEGFA in bone marrow of childred with T-ALL were abnormal, and there was a linear relationship between them. Netrin-1 can interact with its receptor, integrin-β4 and activate AKT transduction pathway to elevate the expression of VEGFA in T-ALL cells.

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