Theander T G, Kharazmi A, Pedersen B K, Christensen L D, Tvede N, Poulsen L K, Odum N, Svenson M, Bendtzen K
Department of Infectious Diseases, Rigshospitalet, Copenhagen, Denmark.
Infect Immun. 1988 Jul;56(7):1673-7. doi: 10.1128/iai.56.7.1673-1677.1988.
This study was undertaken to determine the effect of Pseudomonas aeruginosa alkaline protease (AP) and elastase (ELA) on human lymphocyte function. AP at 50 micrograms/ml and ELA at 12 micrograms/ml caused a 50% inhibition of phytohemagglutinin-induced proliferation. There was no difference in the effect of proteases on CD4- and CD8-positive cells. To determine the effect of proteases on interleukin-2 (IL-2)-induced cell proliferation, the proteases and IL-2 were added to the IL-2-dependent CTLL-2 cell line. AP and ELA inhibited the proliferation of these cells. When IL-2 was added in excess, the inhibition was partly reversed. ELA at 10 micrograms/ml cleaved IL-2, as judged by size chromatography of a reaction mixture containing 125I-labeled IL-2 and the proteases. The ELA-digested IL-2 exhibited a reduced binding capacity to IL-2 receptors on the lymphocytes. Furthermore, treatment of phytohemagglutinin-stimulated lymphocytes with AP and ELA resulted in inhibition of binding of intact IL-2 to IL-2 receptors on the stimulated lymphocytes. These results indicated that P. aeruginosa-derived enzymes are able to interfere with human lymphocyte function in vitro and that this effect might be due to cleavage of IL-2.
本研究旨在确定铜绿假单胞菌碱性蛋白酶(AP)和弹性蛋白酶(ELA)对人淋巴细胞功能的影响。50微克/毫升的AP和12微克/毫升的ELA可使植物血凝素诱导的增殖受到50%的抑制。蛋白酶对CD4阳性和CD8阳性细胞的作用没有差异。为了确定蛋白酶对白细胞介素-2(IL-2)诱导的细胞增殖的影响,将蛋白酶和IL-2添加到依赖IL-2的CTLL-2细胞系中。AP和ELA抑制了这些细胞的增殖。当过量添加IL-2时,抑制作用部分逆转。通过对含有125I标记的IL-2和蛋白酶的反应混合物进行尺寸色谱分析判断,10微克/毫升的ELA可裂解IL-2。经ELA消化的IL-2与淋巴细胞上IL-2受体的结合能力降低。此外,用AP和ELA处理植物血凝素刺激的淋巴细胞会导致完整的IL-2与受刺激淋巴细胞上的IL-2受体结合受到抑制。这些结果表明,铜绿假单胞菌衍生的酶能够在体外干扰人淋巴细胞功能,且这种作用可能是由于IL-2的裂解所致。