Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Toxicol Lett. 2012 Apr 5;210(1):64-70. doi: 10.1016/j.toxlet.2012.01.014. Epub 2012 Feb 1.
Perfluorooctanoic acid (PFOA) has unique physical and chemical characteristics, water and oil repellency, thermal stability, and surfactant properties. PFOA has been regularly found in the blood of animals and humans worldwide, and has become an increasing concern because of its adverse effects in immune system. However, the role of PFOA in the allergic inflammation is not well-known. To further extend the immunotoxicity of PFOA, we examined the role of PFOA on the mast cell-mediated allergic inflammation and studied the possible mechanism of action. PFOA dose- and time-dependently increased histamine release from mast cells and serum histamine by the induction of intracellular calcium. PFOA exacerbated the IgE-dependent local allergic reaction in the mouse allergy model. PFOA induced gene expression of pro-inflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6, and IL-8 in mast cells. The inducing effect of PFOA on the pro-inflammatory cytokines was nuclear factor-κB, p38 mitogen-activated protein kinase, and caspase-1 dependent. Furthermore, the activation of cyclooxygenase-2 by PFOA suggests the induction of allergic inflammatory mediators by the PFOA. Our findings provide evidence that PFOA, the known immunotoxic agent, induces mast cell-derived allergic inflammatory reactions by histamine release and expression of pro-inflammatory cytokines.
全氟辛酸(PFOA)具有独特的物理和化学特性,具有拒水拒油性、热稳定性和表面活性剂特性。PFOA 已在全球范围内的动物和人类血液中经常被发现,由于其对免疫系统的不良影响,已成为人们日益关注的问题。然而,PFOA 在过敏炎症中的作用尚不清楚。为了进一步扩展 PFOA 的免疫毒性,我们研究了 PFOA 对肥大细胞介导的过敏炎症的作用及其可能的作用机制。PFOA 呈剂量和时间依赖性地通过诱导细胞内钙离子增加肥大细胞和血清中的组胺释放。PFOA 加剧了小鼠过敏模型中 IgE 依赖性局部过敏反应。PFOA 诱导肥大细胞中促炎细胞因子如肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β、IL-6 和 IL-8 的基因表达。PFOA 对促炎细胞因子的诱导作用依赖于核因子-κB、p38 丝裂原活化蛋白激酶和半胱天冬酶-1。此外,PFOA 激活环加氧酶-2 表明 PFOA 诱导过敏炎症介质的产生。我们的研究结果表明,已知的免疫毒性物质 PFOA 通过组胺释放和促炎细胞因子的表达诱导肥大细胞来源的过敏炎症反应。