Jonuleit H, Lohmann S, Müller G, Lempertz U, Enk A, Knop J
Department of Dermatology, University of Mainz, Germany.
Arch Dermatol Res. 1996 Nov;288(12):745-52. doi: 10.1007/BF02505291.
Our laboratory has recently developed the monoclonal antibody 4F7 which recognizes a molecule on dendritic cells in the dermis of mice that is upregulated after application of contact allergens in vivo. Furthermore, this antibody detects an antigen on dendritic cells in spleen, lymph nodes and colon. In order to study the influence of contact allergens on the surface expression of the 4F7 molecules on dendritic cells, FACScan analysis of splenic dendritic cells was carried out after in vitro application of contact allergens. Freshly isolated splenic dendritic cells were found to be positive for 4F7, 33D1, N418 (CD11c) and MHC class II. After overnight culture the expression of the dendritic cell-specific molecules 4F7 and 33D1 was decreased. This downregulation was not inhibited by the addition of the cytokines TNF-alpha or GM-CSF during in vitro culture. However, in vitro treatment of freshly isolated dendritic cells with the contact allergen 2,4-dinitrofluorobenzene prevented this downregulation of the 4F7 surface molecules. The same effect was observed after treatment with other contact allergens (1-chloro-2,4-dinitrobenzene or potassium dichromate). Treatment with the irritant substance sodium dodecyl sulphate, the lectins concanavalin and lipopolysaccharide or the phorbol ester PMA did not prevent the downregulation of 4F7 and 33D1. Moreover, the influence of contact allergens on the expression of the molecules 4F7 and 33D1 was not inhibited by the protein synthesis inhibitor cycloheximide. No effects of contact sensitizers were detectable on the expression of MHC class II molecules or the costimulatory molecules B7 and heat-stable antigen. Our results show a specific stabilizing effect of contact allergens on the dendritic cell-specific molecules 4F7 and 33D1 independent of de novo protein synthesis.
我们实验室最近研制出了单克隆抗体4F7,它能识别小鼠真皮树突状细胞上的一种分子,该分子在体内应用接触性变应原后会上调。此外,这种抗体还能检测脾脏、淋巴结和结肠中树突状细胞上的一种抗原。为了研究接触性变应原对树突状细胞上4F7分子表面表达的影响,在体外应用接触性变应原后,对脾树突状细胞进行了流式细胞仪分析。新鲜分离的脾树突状细胞被发现对4F7、33D1、N418(CD11c)和MHC II类分子呈阳性。过夜培养后,树突状细胞特异性分子4F7和33D1的表达降低。在体外培养过程中,添加细胞因子TNF-α或GM-CSF并不能抑制这种下调。然而,用接触性变应原2,4-二硝基氟苯对新鲜分离的树突状细胞进行体外处理可防止4F7表面分子的这种下调。用其他接触性变应原(1-氯-2,4-二硝基苯或重铬酸钾)处理后也观察到了相同的效果。用刺激性物质十二烷基硫酸钠、凝集素伴刀豆球蛋白和脂多糖或佛波酯PMA处理并不能防止4F7和33D1的下调。此外,蛋白质合成抑制剂放线菌酮并不能抑制接触性变应原对4F7和33D1分子表达的影响。未检测到接触性致敏剂对MHC II类分子或共刺激分子B7和热稳定抗原表达的影响。我们的结果表明,接触性变应原对树突状细胞特异性分子4F7和33D1具有特异性稳定作用,且与从头合成蛋白质无关。