Nam Yoon Jeong, Lee Chung Soo
Department of Pharmacology, College of Medicine, and the BK21plus Skin Barrier Network Human Resources Development Team, Chung-Ang University, Seoul, 156-756, South Korea.
Naunyn Schmiedebergs Arch Pharmacol. 2016 Sep;389(9):951-60. doi: 10.1007/s00210-016-1242-6. Epub 2016 May 20.
Keratinocytes may play an important role in the pathogenesis of inflammatory skin diseases. Brefeldin A has been shown to attenuate the production and secretion of chemical mediators involved in inflammation and immune responses. However, the effect of brefeldin A on the TNF-α-stimulated production of inflammatory mediators in keratinocytes has not been studied. We investigated the effect of brefeldin A on the TNF-α-stimulated production of inflammatory mediators using HaCaT cells and primary keratinocytes in relation to the Akt, mTOR, and NF-κB pathways, which regulates the transcription genes involved in immune and inflammatory responses. Brefeldin A, Akt inhibitor, Bay 11-7085 (an inhibitor of NF-κB activation), and rapamycin (mTOR inhibitor) inhibited the TNF-α-stimulated productions of inflammatory mediators, and activations of Akt, mTOR, and NF-κB in keratinocytes. The results show that brefeldin A appears to attenuate TNF-α-stimulated inflammatory mediator production in keratinocytes by suppressing the activation of the Akt, mTOR, and NF-κB pathways.
角质形成细胞可能在炎症性皮肤病的发病机制中发挥重要作用。布雷菲德菌素A已被证明可减少参与炎症和免疫反应的化学介质的产生和分泌。然而,布雷菲德菌素A对角质形成细胞中肿瘤坏死因子-α刺激的炎症介质产生的影响尚未得到研究。我们使用HaCaT细胞和原代角质形成细胞,研究了布雷菲德菌素A对角质形成细胞中肿瘤坏死因子-α刺激的炎症介质产生的影响,该影响与调节参与免疫和炎症反应的转录基因的Akt、mTOR和NF-κB信号通路有关。布雷菲德菌素A、Akt抑制剂、Bay 11-7085(一种NF-κB激活抑制剂)和雷帕霉素(mTOR抑制剂)可抑制角质形成细胞中肿瘤坏死因子-α刺激的炎症介质产生以及Akt、mTOR和NF-κB的激活。结果表明,布雷菲德菌素A似乎通过抑制Akt、mTOR和NF-κB信号通路的激活来减轻肿瘤坏死因子-α刺激的角质形成细胞炎症介质产生。