Rokosz A, Meisel-Mikołajczyk F, Malchar C, Nowaczyk M, Górski A
Katedra i Zakład Mikrobiologii Lekarskiej AM w Warszawie.
Med Dosw Mikrobiol. 2000;52(4):361-73.
The aim of this study was to assay the degree of human T lymphocyte and granulocyte adhesion to the vascular endothelial cells stimulated by Bacteroides thetaiotaomicron lipopolysaccharides, components of LPS and capsular polysaccharide. HMEC-1 cells were activated with bacterial preparations in concentration 10 micrograms/ml for 4 and 24 hours. T lymphocytes and granulocytes were isolated from peripheral blood of healthy blood donors. Thereafter, the adhesion tests of granulocytes and adhesion tests of non-activated and activated with PMA (in concentration 10 ng/ml) T lymphocytes to the resting and stimulated vascular endothelium were performed. The number of viable cells, which adhered to the endothelium, was determined using inverted microscope (magnification 200x). The results were presented as the number of viable cells adhering to 1 mm2 of the endothelial cell culture. The obtained results indicate that granulocytes and T lymphocytes (resting and activated with PMA) adhere to the endothelial cells stimulated by B. thetaiotaomicron cell-surface antigens. B. thetaiotaomicron lipopolysaccharides and capsular polysaccharide are weaker stimulants of human leukocyte adhesion to the HMEC-1 cells than E. coli O55:B5 LPS.
本研究的目的是测定人T淋巴细胞和粒细胞对由具核梭杆菌脂多糖、脂多糖成分和荚膜多糖刺激的血管内皮细胞的黏附程度。用浓度为10微克/毫升的细菌制剂激活HMEC-1细胞4小时和24小时。从健康献血者的外周血中分离出T淋巴细胞和粒细胞。此后,进行粒细胞的黏附试验以及未激活的和用佛波酯(浓度为10纳克/毫升)激活的T淋巴细胞对静息和受刺激血管内皮的黏附试验。使用倒置显微镜(放大倍数为200倍)确定黏附于内皮的活细胞数量。结果以黏附于1平方毫米内皮细胞培养物的活细胞数量表示。所得结果表明,粒细胞和T淋巴细胞(静息的和用佛波酯激活的)黏附于由具核梭杆菌细胞表面抗原刺激的内皮细胞。与大肠杆菌O55:B5脂多糖相比,具核梭杆菌脂多糖和荚膜多糖对人白细胞黏附于HMEC-1细胞的刺激作用较弱。