Department of Physiology, National Yang-Ming University, Taipei, Taiwan.
J Nutr Biochem. 2011 Nov;22(11):1015-21. doi: 10.1016/j.jnutbio.2010.08.014. Epub 2010 Dec 28.
Wogonin, one component in Scutellaria baicalensis Georgi extracts, has several beneficial properties for cancers and inflammatory diseases. However, the efficacy of wogonin in cholesterol metabolism of macrophages remains unknown. In macrophages, cholesterol uptake is controlled by scavenger receptors (SR-A and CD36) and cholesterol efflux by SR-BI, ATP-binding cassette transporter-A1 (ABCA1) and ABCG1. In the present study, we investigated the effect and underlying molecular mechanism of wogonin on the formation of macrophage foam cells by murine J774.A1 macrophages. Wogonin attenuated oxidized low-density lipoprotein (oxLDL)-induced cholesterol accumulation in macrophages. The binding of oxLDL to macrophages and protein expression of SR-A and CD36 were not affected by wogonin. Wogonin enhanced cholesterol efflux and increased the protein level of ABCA1 without affecting the protein expression of SR-BI or ABCG1. Inhibition of ABCA1 by pharmacological inhibitor 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid disodium salt or neutralizing antibody abolished this suppressive effect of wogonin on lipid accumulation. Moreover, the up-regulation of ABCA1 protein by wogonin resulted from a decrease in degradation rate of ABCA1 protein, with no effect on ABCA1 mRNA expression. This reduction in ABCA1 degradation was due to increased protein phosphatase 2B (PP2B)-mediated ABCA1 dephosphorylation, as evidenced by increased interaction between ABCA1 and PP2B; pharmacological inhibition of PP2B would prevent wogonin-induced ABCA1 protein expression, dephosphorylation and attenuation of lipid accumulation. Collectively, wogonin increases the protein stability of ABCA1 via PP2B-mediated dephosphorylation, thus leading to reduced cholesterol accumulation in macrophage foam cells.
汉黄芩素是黄芩提取物的一种成分,具有多种抗癌和抗炎作用。然而,汉黄芩素在巨噬细胞胆固醇代谢中的功效尚不清楚。在巨噬细胞中,胆固醇摄取受清道夫受体(SR-A 和 CD36)控制,胆固醇外排由 SR-BI、ATP 结合盒转运体 A1(ABCA1)和 ABCG1 介导。本研究旨在探讨汉黄芩素对 J774.A1 巨噬细胞泡沫细胞形成的影响及潜在分子机制。汉黄芩素可减轻氧化型低密度脂蛋白(oxLDL)诱导的巨噬细胞胆固醇蓄积。汉黄芩素不影响 oxLDL 与巨噬细胞的结合以及 SR-A 和 CD36 的蛋白表达。汉黄芩素增强胆固醇外排,增加 ABCA1 蛋白水平,而不影响 SR-BI 或 ABCG1 的蛋白表达。ABCA1 的药理学抑制剂 4,4'-二异硫氰酸基二苯乙烯-2,2'-二磺酸二钠盐或中和抗体抑制 ABCA1 可消除汉黄芩素对脂质蓄积的抑制作用。此外,汉黄芩素上调 ABCA1 蛋白的作用是由于 ABCA1 蛋白降解率降低,而 ABCA1 mRNA 表达无变化。ABCA1 降解减少是由于蛋白磷酸酶 2B(PP2B)介导的 ABCA1 去磷酸化增加所致,这可通过 ABCA1 与 PP2B 之间的相互作用增强来证明;PP2B 的药理学抑制可阻止汉黄芩素诱导的 ABCA1 蛋白表达、去磷酸化和脂质蓄积减少。综上所述,汉黄芩素通过 PP2B 介导的去磷酸化增加 ABCA1 的蛋白稳定性,从而减少巨噬细胞泡沫细胞中的胆固醇蓄积。