Department of Pharmacology, School of Medicine, Pusan National University, Busan 602-739, Korea.
Korean J Physiol Pharmacol. 2008 Aug;12(4):171-6. doi: 10.4196/kjpp.2008.12.4.171. Epub 2008 Aug 31.
Heat shock proteins (HSPs) serve as molecular chaperones and play a role in cell protection from damage in response to stress stimuli. The aim of this article is to investigate whether HSP22 affects IL-8 expression in vascular smooth muscle cells (VSMCs), and which cellular factors are involved in the HSP-mediated IL-8 induction in that cell type in terms of mitogen activated protein kinase (MAPK) and transcription element. Exposure of aortic smooth muscle cells (AoSMCs) to HSP22 not only enhanced IL-8 release but also induced IL-8 transcript via promoter activation. HSP22 activated ERK and p38 MAPK in AoSMCs. HSP22-induced IL-8 release was inhibited by U0126, but not by SB202190. A mutation in the IL-8 promoter region at the binding site of NF-kappaB, but not AP-1 or C/EBP, impaired promoter activation in response to HSP22. Delivery of IkappaB, but not dominant negative c-Jun, lowered HSP22-induced IL-8 release from AoSMCs. These results suggest that HSP22 induces IL-8 in VSMCs via ERK1/2, and that transcription factor NF-kB may be required for the HSP22-induced IL-8 up-regulation.
热休克蛋白 (HSPs) 作为分子伴侣,在细胞受到应激刺激时发挥保护作用,防止损伤。本文旨在研究 HSP22 是否影响血管平滑肌细胞 (VSMCs) 中 IL-8 的表达,以及 HSP 介导的该细胞类型中 IL-8 诱导的细胞因子在丝裂原活化蛋白激酶 (MAPK) 和转录因子方面的作用。HSP22 暴露于主动脉平滑肌细胞 (AoSMCs) 不仅增强了 IL-8 的释放,还通过启动子激活诱导了 IL-8 转录。HSP22 在 AoSMCs 中激活了 ERK 和 p38 MAPK。U0126 抑制 HSP22 诱导的 IL-8 释放,但 SB202190 则无此作用。在 HSP22 反应性启动子区域中,NF-κB 结合位点的 IL-8 启动子区域发生突变,但 AP-1 或 C/EBP 则无此作用,从而损害了启动子的激活。IkappaB 的传递,而不是显性负性 c-Jun,则降低了 HSP22 诱导的 AoSMCs 中 IL-8 的释放。这些结果表明,HSP22 通过 ERK1/2 诱导 VSMCs 中的 IL-8,并且 HSP22 诱导的 IL-8 上调可能需要转录因子 NF-κB。