Puthengady Thomas Bina, Sun Chun Xiang, Bajenova Elena, Ellen Richard P, Glogauer Michael
CIHR Group in Matrix Dynamics and Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada M5S 3E2.
Infect Immun. 2006 Mar;74(3):1954-7. doi: 10.1128/IAI.74.3.1954-1957.2006.
In this study of human polymorphonuclear leukocytes (PMNs), pretreatment with Treponema denticola major outer sheath protein (Msp) inhibited formyl-methionyl-leucyl-phenylalanine (fMLP)-induced chemotaxis, phagocytosis of immunoglobulin G-coated microspheres, fMLP-stimulated calcium transients, and actin assembly. Msp neither altered oxidative responses to phorbol myristate or fMLP nor induced apoptosis. Msp selectively impairs chemotaxis and phagocytosis by impacting the PMN cytoskeleton.
在这项针对人类多形核白细胞(PMNs)的研究中,用齿垢密螺旋体主要外鞘蛋白(Msp)进行预处理可抑制甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)诱导的趋化作用、免疫球蛋白G包被微球的吞噬作用、fMLP刺激的钙瞬变以及肌动蛋白组装。Msp既不改变对佛波酯或fMLP的氧化反应,也不诱导细胞凋亡。Msp通过影响PMN细胞骨架选择性地损害趋化作用和吞噬作用。