Santos L L, Huang X R, Berndt M C, Holdsworth S R
Centre for Inflammatory Diseases, Monash University, Monash Medical Centre, Clayton, Victoria, Australia.
Clin Exp Immunol. 1998 May;112(2):281-6. doi: 10.1046/j.1365-2249.1998.00584.x.
The aim of this study was to investigate the role of P-selectin in the accumulation of neutrophils in the direct passive Arthus reaction in rat skin. Direct passive Arthus dermal reaction was induced in male Sprague-Dawley (SD) rats by a single i.v. injection of rat anti-sheep globulin (SG) 1 h before i.d. injection of SG antigen. Anti-P-selectin or irrelevant control antibody was given 1 h before rat anti-SG injection. Complement depletion was also performed in a separate group by pretreatment with cobra venom factor (CVF). In all groups dermal swelling was assessed 4 h after antigen challenge. Four hours after antigen challenge, rats treated with control antibody developed skin swelling (2.29 +/- 0.47 mm), prominent complement deposition and neutrophil accumulation. This response was associated with local up-regulation of endothelial P-selectin. Pre-treatment with anti-P-selectin antibody 1 h before passive Arthus induction prevented skin swelling (0.29 +/- 0.06 mm, P < 0.05, cf with control antibody treatment), neutrophil accumulation and up-regulation of endothelial P-selectin despite complement deposition. CVF treatment prevented complement deposition, neutrophil accumulation and skin swelling (0.13 +/- 0.07 mm, P < 0.05, cf with saline treatment). However, endothelial P-selectin expression was still present. Inhibition of skin swelling and neutrophil accumulation in direct passive Arthus by functional inhibition of P-selectin suggest a pivotal role for this adhesion molecule in this inflammatory process. These results also suggest that multiple steps are involved in the evolution of direct passive Arthus, including both P-selectin expression and complement activation. However, while complement activation is essential for neutrophil accumulation and expression of dermal injury, P-selectin up-regulation initiated by antibody/antigen deposition occurs independently of complement activation.
本研究旨在探讨P-选择素在大鼠皮肤直接被动Arthus反应中嗜中性粒细胞聚集过程中的作用。在雄性Sprague-Dawley(SD)大鼠中,于皮内注射SG抗原前1小时经静脉单次注射大鼠抗羊球蛋白(SG)诱导直接被动Arthus皮肤反应。在注射大鼠抗SG前1小时给予抗P-选择素或无关对照抗体。另一组通过用眼镜蛇毒因子(CVF)预处理进行补体耗竭。在所有组中,抗原激发后4小时评估皮肤肿胀情况。抗原激发后4小时,用对照抗体处理的大鼠出现皮肤肿胀(2.29±0.47毫米)、明显的补体沉积和嗜中性粒细胞聚集。该反应与内皮P-选择素的局部上调有关。在被动Arthus诱导前1小时用抗P-选择素抗体预处理可防止皮肤肿胀(0.29±0.06毫米,P<0.05,与对照抗体处理相比)、嗜中性粒细胞聚集以及内皮P-选择素的上调,尽管有补体沉积。CVF处理可防止补体沉积、嗜中性粒细胞聚集和皮肤肿胀(0.13±0.07毫米,P<0.05,与盐水处理相比)。然而,内皮P-选择素表达仍然存在。通过功能性抑制P-选择素抑制直接被动Arthus中的皮肤肿胀和嗜中性粒细胞聚集表明该黏附分子在这一炎症过程中起关键作用。这些结果还表明,直接被动Arthus的演变涉及多个步骤,包括P-选择素表达和补体激活。然而,虽然补体激活对于嗜中性粒细胞聚集和皮肤损伤表达至关重要,但由抗体/抗原沉积引发的P-选择素上调独立于补体激活发生。