Department of Pharmacology, School of Medicine and Institute of Health Sciences, Gyeongsang National University, Jinju, Korea.
J Agric Food Chem. 2009 Aug 26;57(16):7324-30. doi: 10.1021/jf900856z.
Adhesion molecules have a key role in pathological inflammation. Thus, we investigated the effect of anthocyanins on the induction of intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) by TNF-alpha and the possible molecular mechanisms by which anthocyanins differentially regulate ICAM-1 and VCAM-1 expression. Stimulation of cells with TNF-alpha increased ICAM-1 and VCAM-1 expression, and pretreatment with anthocyanins inhibited VCAM-1 expression, but not ICAM-1 expression. We found that IRF-1 and GATAs, especially GATA-4 and -6, were involved in the TNF-alpha-mediated expression of VCAM-1 but not ICAM-1, and anthocyanins decreased nuclear levels of GATA-4 and GATA-6 as well as IRF-1. Moreover, pretreatment with a Jak/STAT inhibitor decreased TNF-alpha-induced VCAM-1 expression and nuclear GATA-4, GATA-6, and IRF-1 levels. Furthermore, anthocyanins efficiently inhibited the phosphorylation of STAT-3. This suggests that anthocyanins differentially regulate TNF-alpha-mediated expression of VCAM-1 and ICAM-1 through modulation of the GATA and IRF-1 binding activity via Jak/STAT-3 activation.
黏附分子在病理性炎症中起着关键作用。因此,我们研究了花色苷对 TNF-α诱导的细胞间黏附分子-1(ICAM-1)和血管细胞黏附分子-1(VCAM-1)的诱导作用,以及花色苷通过何种可能的分子机制差异调控 ICAM-1 和 VCAM-1 的表达。TNF-α刺激细胞会增加 ICAM-1 和 VCAM-1 的表达,花色苷预处理可抑制 VCAM-1 的表达,但不影响 ICAM-1 的表达。我们发现,IRF-1 和 GATA 因子(尤其是 GATA-4 和 GATA-6)参与了 TNF-α介导的 VCAM-1 表达,但不参与 ICAM-1 的表达,花色苷还降低了核内 GATA-4 和 GATA-6 以及 IRF-1 的水平。此外,Jak/STAT 抑制剂预处理可降低 TNF-α诱导的 VCAM-1 表达和核内 GATA-4、GATA-6 和 IRF-1 水平。此外,花色苷可有效抑制 STAT-3 的磷酸化。这表明,花色苷通过 Jak/STAT-3 激活来调节 GATA 和 IRF-1 结合活性,从而差异调控 TNF-α 介导的 VCAM-1 和 ICAM-1 的表达。