School of Food Science and Engineering, Lingnan Normal University, Zhanjiang 504048, China.
School of Life Science and Technology, Lingnan Normal University, Zhanjiang 524048, China.
Molecules. 2022 Dec 7;27(24):8639. doi: 10.3390/molecules27248639.
There is increasing evidence supporting a role for enhanced macrophage cholesterol efflux in ameliorating atherosclerosis. Opuntia dillenii Haw. polysaccharide (ODP-Ia), the most important functional component obtained from Opuntia dillenii Haw. stem, has anti-atherosclerosis effects. Therefore, we propose that ODP-Ia could promote cholesterol efflux via the PPARγ-LXRα signaling pathway. In this study, THP-1 foam cells derived from macrophages were treated with different concentrations of ODP-Ia, GGPP (antagonist of LXRα) and GW9662 (antagonist of PPARγ), with or without 15 nmol ODP-Ia. The total cholesterol content in the cells was measured. The mRNA of ABCA1, ABCG1, PPARγ, LXRα and their protein levels in the foam cells were detected by RT−PCR and Western blot, respectively. The results showed that ODP-Ia plays a role in significantly promoting cholesterol efflux (p < 0.05) by upregulating the expression of ABCA1, ABCG1, SR-BI, PPARγ, PPARα and LXRα. Meanwhile, PPARγ and LXRα antagonists dramatically interfered the cholesterol efflux mediated by ODP-Ia (p < 0.05) and dramatically inhibited the upregulating effect of ODP-Ia on the expression of PPARγ, LXRα, ABCA1 and ABCG1 at both protein and mRNA levels (p < 0.05). In conclusion, ODP-Ia promotes cholesterol efflux in the foam cells through activating the PPARγ-LXRα signaling pathway. This bioactivity suggested that ODP-Ia may be of benefit in treating atherosclerosis.
越来越多的证据表明,增强巨噬细胞胆固醇外排在改善动脉粥样硬化方面具有重要作用。仙人掌多糖(ODP-Ia)是从仙人掌茎中提取的最重要的功能成分,具有抗动脉粥样硬化作用。因此,我们提出 ODP-Ia 可以通过 PPARγ-LXRα 信号通路促进胆固醇外流。在这项研究中,用不同浓度的 ODP-Ia、GGPP(LXRα 拮抗剂)和 GW9662(PPARγ 拮抗剂)处理源自巨噬细胞的 THP-1 泡沫细胞,或不处理,用或不用 15 nmol ODP-Ia。测量细胞内总胆固醇含量。用 RT−PCR 和 Western blot 分别检测泡沫细胞中 ABCA1、ABCG1、PPARγ、LXRα 的 mRNA 及其蛋白水平。结果表明,ODP-Ia 通过上调 ABCA1、ABCG1、SR-BI、PPARγ、PPARα 和 LXRα 的表达,在显著促进胆固醇外流方面发挥作用(p<0.05)。同时,PPARγ 和 LXRα 拮抗剂显著干扰 ODP-Ia 介导的胆固醇外流(p<0.05),并显著抑制 ODP-Ia 对 PPARγ、LXRα、ABCA1 和 ABCG1 的表达的上调作用,无论是在蛋白水平还是在 mRNA 水平上(p<0.05)。综上所述,ODP-Ia 通过激活 PPARγ-LXRα 信号通路促进泡沫细胞中的胆固醇外流。这种生物活性表明,ODP-Ia 可能有益于治疗动脉粥样硬化。