Clinical Experiment Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Biomed Res Int. 2013;2013:206061. doi: 10.1155/2013/206061. Epub 2012 Dec 20.
Local inflammation is a prominent characteristic of snakebite wound, and snake-venom phospholipase A2s (PLA2s) are some of the main component that contribute to accumulation of inflammatory cells. However, the action of an R49 PLA2s, promutoxin from Protobothrops mucrosquamatus venom, on mast-cell accumulation has not been previously examined. Using a mouse peritoneal model, we found that promutoxin can induce approximately-6-fold increase in mast-cell accumulation, and the response lasts at least for 16 h. The promutoxin-induced mast cell accumulation was inhibited by cyproheptadine, terfenadine, and Ginkgolide B, indicating that histamine and platelet-activating factor (PAF) is likely to contribute to the mast-cells accumulation. Preinjection of antibodies against adhesion molecules ICAM-1, CD18, CD11a, and L-selectin showed that ICAM-1, and CD18, CD11a are key adhesion molecules of promutoxin-induced mast-cell accumulation. In conclusion, promutoxin can induce accumulation of mast cells, which may contribute to snake-venom wound.
局部炎症是蛇伤的一个显著特征,蛇毒磷脂酶 A2(PLA2)是导致炎症细胞积聚的主要成分之一。然而,R49 PLA2s(如来自尖吻蝮蛇毒的原促栓酶)对肥大细胞积聚的作用尚未被研究过。在小鼠腹腔模型中,我们发现原促栓酶可诱导约 6 倍的肥大细胞积聚,该反应至少持续 16 小时。普莫毒素诱导的肥大细胞积聚可被赛庚啶、特非那定和银杏内酯 B 抑制,表明组胺和血小板激活因子(PAF)可能参与了肥大细胞的积聚。预先注射针对细胞间黏附分子 ICAM-1、CD18、CD11a 和 L-选择素的抗体表明,ICAM-1 和 CD18、CD11a 是原促栓酶诱导的肥大细胞积聚的关键黏附分子。总之,原促栓酶可诱导肥大细胞积聚,这可能有助于蛇伤的发生。