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槐多糖通过 PPARγ-LXRα 信号通路促进 THP-1 源性泡沫细胞胆固醇外流。

Haw. Polysaccharide Promotes Cholesterol Efflux in THP-1-Derived Foam Cells via the PPARγ-LXRα Signaling Pathway.

机构信息

School of Food Science and Engineering, Lingnan Normal University, Zhanjiang 504048, China.

School of Life Science and Technology, Lingnan Normal University, Zhanjiang 524048, China.

出版信息

Molecules. 2022 Dec 7;27(24):8639. doi: 10.3390/molecules27248639.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4976/9781717/84aedc86af9d/molecules-27-08639-g001.jpg

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