克林霉素、甲硝唑和多粘菌素B对脆弱拟杆菌内毒素和肠毒素诱导的细胞粘附分子表达的影响。

Acta microbiologica Polonica Pub Date : 2003-01-01
Felicja Meisel-Mikołajczyk, Alicja Rokosz, Katarzyna Kot, Elwira Zawidzka, Cezary Malchar, Maria Nowaczyk, Andrzej Górski
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引用次数: 0

摘要

本研究的目的是比较抗菌剂(克林霉素、甲硝唑和多粘菌素B)对LPS和肠毒素刺激HMEC-1细胞株黏附分子(VCAM-1、ICAM-1和e -选择素)表达的影响。LPS提取自两个参考菌株:ATCC 43858和NCTC 11295,以及一个实验室分离的产肠毒素菌株(W2)和一个非产肠毒素参考菌株IPL E 323。从脆弱芽孢杆菌ATCC 43858培养基中分离得到肠毒素制剂Tox 1和Tox 2,并对其进行纯化。用浓度为10 mg/ml的细菌制剂刺激HMEC-1细胞株。采用ELISA法测定黏附分子的表达。克林霉素、甲硝唑和多粘菌素B均可抑制脆弱芽孢杆菌LPS刺激内皮细胞时ICAM-1的表达,而Tox -1和Tox - 2可增强ICAM-1的表达。当LPS或肠毒素刺激内皮细胞时,抗微生物药物增强了VCAM-1的表达。e -选择素表达分化。
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Influence of clindamycin, metronidazole and polymyxin B on the expression of cell adhesion molecules stimulated by endotoxin and enterotoxin of Bacteroides fragilis.

The aim of this study was to compare the influence of antimicrobials (clindamycin, metronidazole and polymyxin B) on the expression of adhesion molecules (VCAM-1, ICAM-1 and E-selectin) on the HMEC-1 cell line stimulated by LPS and enterotoxin of B. fragilis. LPS was extracted from two reference: ATCC 43858 and NCTC 11295 and one isolated in our laboratory (W2) enterotoxigenic strains, and one nonenterotoxigenic reference strain--IPL E 323. Enterotoxin preparations (Tox 1 and Tox 2) were isolated from supematant of B. fragilis ATCC 43858 culture and purified. HMEC-1 cell line was stimulated with bacterial preparations at concentration of 10 mg/ml. For measuring the expression of adhesion molecules we used ELISA test. Clindamycin, metronidazole and polymyxin B supressed the ICAM-1 expression when endothelium was stimulated with B. fragilis LPS and augmented ICAM-1 expression by Tox 1 and Tox 2. The expression of VCAM-1 was augmented by antimicrobials when endothelium was stimulated with LPS or enterotoxin preparations. The expression of E-selectin was differentiated.

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