Skoutelis A T, Kaleridis V E, Gogos C A, Athanassiou G M, Missirlis Y F, Bassaris H P
Section of Infectious Diseases, Patras University Medical School, Patras, Greece.
Cytokine. 2000 Nov;12(11):1737-40. doi: 10.1006/cyto.2000.0761.
Cytokines are potent polymorphonuclear leukocyte (PMN) activators and can decrease their deformability. We evaluated passive PMN deformability using the micropipette method after incubation with different concentrations of lipopolysaccharide (LPS), interleukins (IL-) 1, 6, 8 and 10, tumour necrosis factor (TNF), granulocyte (G) and granulocyte-macrophage (GM) colony-stimulating factors (CSF). TNF, IL-1, G-CSF, GM-CSF and, to a lesser degree, IL-6 significantly and in a dose-dependent fashion decrease PMN deformability. LPS had no direct effect on PMN deformability. When cytokines at concentrations with no effect on deformability were combined they increased PMN rigidity. The findings suggest that several cytokines and CSF impair directly, and not by activation alone, PMN deformability.
细胞因子是强效的多形核白细胞(PMN)激活剂,可降低其变形能力。我们在不同浓度的脂多糖(LPS)、白细胞介素(IL-)1、6、8和10、肿瘤坏死因子(TNF)、粒细胞(G)和粒细胞-巨噬细胞(GM)集落刺激因子(CSF)孵育后,使用微量移液器法评估了被动PMN变形能力。TNF、IL-1、G-CSF、GM-CSF以及在较小程度上IL-6以剂量依赖性方式显著降低PMN变形能力。LPS对PMN变形能力无直接影响。当将对变形能力无影响浓度的细胞因子联合使用时,它们会增加PMN的刚性。这些发现表明,几种细胞因子和CSF直接损害PMN变形能力,而不仅仅是通过激活来实现。