Ezrin基因沉默通过降低Calpain-1活性抑制血管紧张素Ⅱ诱导的ABCA1降解
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(1.贵州医科大学;2.贵州医科大学附属医院综合病房;3.贵州省医学分子生物学重点实验室,贵州省贵阳市 550004)

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王兰,硕士研究生,主要研究方向为动脉粥样硬化的发病机制与防治,E-mail为18615393387@ 163.com。

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国家自然科学基金(31260250和31660288)资助项目


Ezrin silencing inhibits angiotensin Ⅱ-induced ABCA1 decrease by reducing calpain-1 activity
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1.Guizhou Medical University;2.Department of Comprehensive Ward, the Affiliated Hospital of Guizhou Medical University;3.Guizhou Key Laboratory of Medical Molecular Biology, Guizhou Medical University, Guiyang, Guizhou 550004, China)

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    摘要:

    目的 探讨埃兹蛋白(Ezrin)基因表达降低对RAW264.7钙激活中性半胱氨酸蛋白酶(Calpain-1)活性及三磷酸腺苷结合盒转运体A1(ABCA1)蛋白表达的影响。 方法 实时荧光定量PCR及Western blot法分别检测靶向作用于Ezrin基因的小干扰RNA(siRNA )的抑制效率。Western blot法检测血管紧张素Ⅱ(AngⅡ)及联合加入Ezrin siRNA后Calpain-1的蛋白表达水平变化。Western blot法检测AngⅡ及联合加入Calpain抑制剂N-乙酰基-L-亮氨酰-L-亮氨酰-L-正亮氨酸(ALLN)、Ezrin siRNA 后对ABCA1蛋白表达水平的影响。 结果 Ezrin siRNA转染组较对照组Ezrin的mRNA和蛋白表达均下调(P<0.05)。Western blot结果显示AngⅡ可上调Calpain-1的活性(4.92±0.23比1.00±0.17,P<0.05),而Ezrin siRNA可逆转Calpain-1的活性上调(0.23±0.21比4.92±0.23, P<0.05)。此外,AngⅡ处理后ABCA1蛋白表达下调(0.167±0.055比0.732±0.072,P<0.05),这种作用可被Ezrin siRNA逆转(0.611±0.048比0.167±0.055,P<0.05),而给予Calpain抑制剂ALLN干预未能进一步提高ABCA1蛋白水平。 结论Ezrin可能通过Calpain-1途径在AngⅡ诱导的ABCA1表达降低过程中发挥重要作用。

    Abstract:

    Aim To investigate the effects of Ezrin gene knockout on calpain-1 activity and adenosine triphosphate binding cassette transporter A1(ABCA1) protein levels in RAW264.7 cells. Methods RAW264.7 cells transfected with small interfering RNA (siRNA) targeting Ezrin were subject to real time PCR and Western blot to detect the inhibition ratio. Added with angiotension Ⅱ(AngⅡ) or AngⅡ+ Ezrin siRNA, calpain-1 protein expression and activity were determined by using Western blot. Then, the expression of ABCA1 protein was examined by Western blot after the treatment with AngⅡ,Ezrin siRNA, calpain inhibitor N-acetyl-L-leucyl-L-leucyl-L-norleucine (ALLN). Results Ezrin mRNA and protein expression in Ezrin siRNA groups were inhibited(P<0.05). The calpain-1 expression were upregulated by AngⅡ treatment (4.92±0.23 vs 1.00±0.17, P<0.05), which were reversed by Ezrin siRNA (0.23±0.21 vs 4.92±0.23, P<0.05). Therefore, the ABCA1 protein expression was inhibited by addition of AngⅡ(0.167±0.055 vs 0.732±0.072), which were reversed by Ezrin siRNA (0.611±0.048 vs 0.167±0.055, P<0.05). There were no statistically significant differences at ABCA1 protein levels between AngⅡ+Ezrin siRNA group and AngⅡ+Ezrin siRNA+ALLN group. Conclusion Ezrin might play an important role in AngⅡ-induced ABCA1 protein attenuation via calpain-1 pathway.

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王兰,郭静,莫显刚,安静,张莉,洪伟. Ezrin基因沉默通过降低Calpain-1活性抑制血管紧张素Ⅱ诱导的ABCA1降解[J].中国动脉硬化杂志,2018,26(3):217~221.

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  • 收稿日期:2017-11-20
  • 最后修改日期:2018-01-08
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  • 在线发布日期: 2018-04-03