油酰乙醇胺通过过氧化物酶体增殖物激活受体α途径抑制单核-内皮细胞的黏附作用
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(厦门医学院生物制药室,福建省厦门市 361023)

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李莹,博士,讲师,研究方向为心血管药理学,E-mail为yanglc00@163.com。

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福建省自然科学基金(2016D024)


Oleoylethanolamide inhibits monocyte-endothelial cell adhesion through peroxisome proliferator-activated receptor α pathway
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Biopharmaceutical Laboratory, Xiamen Medical College, Xiamen, Fujian 361023, China)

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    摘要:

    目的 探讨过氧化物酶体增殖物激活受体α(PPARα)激动剂油酰乙醇胺(OEA)对单核-内皮细胞黏附作用的影响。方法 采用Western blot检测OEA对脂多糖诱导THP-1细胞中基质金属蛋白酶2(MMP-2)和MMP-9蛋白表达及对肿瘤坏死因子α(TNF-α)诱导人脐静脉内皮细胞中血管细胞黏附分子1(VCAM-1)和细胞间黏附分子1(ICAM-1)蛋白表达的影响。采用TNF-α诱导的单核-内皮细胞黏附模型,用PPARα阻断剂MK886阻断PPARα信号通路后,检测THP-1细胞的黏附和VCAM-1蛋白的表达。结果 40 μmol/L OEA显著抑制MMP-2、MMP-9、VCAM-1和ICAM-1蛋白表达。OEA对TNF-α诱导的单核-内皮细胞黏附具有直接的抑制作用。MK886部分逆转了OEA对单核-内皮细胞黏附的抑制作用及对VCAM-1蛋白表达的抑制作用。结论 OEA能够抑制单核-内皮细胞的黏附,其机制可能与PPARα途径相关。

    Abstract:

    Aim To investigate the effect of peroxisome proliferator-activated receptor α (PPARα) agonist oleoylethanolamide (OEA) on the adhesion of monocytes to endothelial cells. Methods Western blot was used to detect the effects of OEA on the expressions of matrix metalloproteinase-2 (MMP-2) and MMP-9 in lipopolysaccharide-induced THP-1 cells and the expressions of vascular cell adhesion molecule-1 (VCAM-1) and intercellular cell adhesion molecule-1 (ICAM-1) in human umbilical vein endothelial cells induced by tumor necrosis factor α (TNF-α). The adhesion of THP-1 cells and the expression of VCAM-1 protein were detected by TNF-α-induced monocyte-endothelial cell adhesion model after PPARα blocker MK886 blocked PPARα signaling pathway. Results 40 μmol/L OEA significantly inhibited MMP-2, MMP-9, VCAM-1 and ICAM-1 protein expression. OEA had a direct inhibitory effect on the monocyte-endothelial cell adhesion induced by TNF-α. MK886 partially reversed the inhibitory effect of OEA on monocyte-endothelial cell adhesion and VCAM-1 protein expression. Conclusion OEA can inhibit the adhesion of monocytes to endothelial cells, and its mechanism may be related to PPARα pathway.

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李莹,王英,曾臻,杨丙晔,罗浩虹.油酰乙醇胺通过过氧化物酶体增殖物激活受体α途径抑制单核-内皮细胞的黏附作用[J].中国动脉硬化杂志,2018,26(10):1006~1010.

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  • 收稿日期:2018-04-13
  • 最后修改日期:2018-06-19
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  • 在线发布日期: 2018-11-09