首页> 美国卫生研究院文献>BMB Reports >23-Dimethoxy-2′-hydroxychalcone ameliorates TNF-α-induced ICAM-1 expression and subsequent monocyte adhesiveness via NF-kappaB inhibition and HO-1 induction in HaCaT cells
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23-Dimethoxy-2′-hydroxychalcone ameliorates TNF-α-induced ICAM-1 expression and subsequent monocyte adhesiveness via NF-kappaB inhibition and HO-1 induction in HaCaT cells

机译:23-二甲氧基-2-羟基查尔酮通过HaCaT细胞中的NF-κB抑制和HO-1诱导来改善TNF-α诱导的ICAM-1表达和随后的单核细胞粘附性

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摘要

Up-regulation of adhesion molecules plays an important role in the infiltration of leukocytes into the skin during the development of various inflammatory skin diseases, such as atopic dermatitis. In this study, we investigated the modulatory effects of 2,3-dimethoxy-2′-hydroxychalcone (DMHC) on tumor necrosis factor (TNF)-α-induced intercellular adhesion molecule-1 (ICAM-1) expression and monocyte adhesiveness, as well as the molecular mechanisms underlying its action in the HaCaT human keratinocyte cell line. Pre-treating HaCaT cells with DMHC significantly suppressed TNF-α-induced ICAM-1 expression and subsequent monocyte adhesiveness. DMHC inhibited TNF-α-induced activation of NF-ᴋB. In addition, DMHC induced HO-1 expression as well as NRF2 activation. Furthermore, HO-1 knockdown using siRNA reversed the inhibitory effect of DMHC on TNF-α-induced ICAM-1 expression and adhesion of monocytes to keratinocytes. These results suggest that DMHC may inhibit TNF-α-induced ICAM-1 expression and adhesion of monocytes to keratinocytes by suppressing the signaling cascades leading to NF-ᴋB activation and inducing HO-1 expression in keratinocytes. [BMB Reports 2016; 49(1): 57-62]
机译:在各种炎症性皮肤病如特应性皮炎的发展过程中,粘附分子的上调在白细胞向皮肤的浸润中起重要作用。在这项研究中,我们研究了2,3-二甲氧基-2'-羟基查尔酮(DMHC)对肿瘤坏死因子(TNF)-α诱导的细胞间黏附分子1(ICAM-1)表达和单核细胞黏附的调节作用,如下以及其在HaCaT人角质形成细胞系中作用的分子机制。用DMHC预处理HaCaT细胞可显着抑制TNF-α诱导的ICAM-1表达和随后的单核细胞粘附性。 DMHC抑制TNF-α诱导的NF-ᴋB活化。此外,DMHC诱导HO-1表达以及NRF2激活。此外,使用siRNA进行HO-1敲低逆转了DMHC对TNF-α诱导的ICAM-1表达以及单核细胞与角质形成细胞粘附的抑制作用。这些结果表明,DMHC可通过抑制导致NF-κB活化的信号级联反应并诱导角质形成细胞中HO-1的表达来抑制TNF-α诱导的ICAM-1表达和单核细胞对角质形成细胞的粘附。 [BMB报告2016; 49(1):57-62]

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