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作 者:肖刚[1] 郭青玉[1] 李睿[1] 吴军正[2] 邓晓红[1] 张铁良[1]
机构地区:[1]西安交通大学口腔医院口腔内科教研室,710004 [2]西安第四军医大学口腔医院
出 处:《实用口腔医学杂志》2007年第4期519-522,共4页Journal of Practical Stomatology
摘 要:目的:筛选一种适合变形链球菌的寡核苷酸转运方法,为利用反义寡核苷酸抑制变形链球菌基因表达打下基础。方法:分别采用阳离子聚合体So-fastTM,及阳离子脂质体为载体,以FITC标记的寡核苷酸转化变形链球菌,流式细胞术检测摄取率,并与自然转化和电穿孔转化法的摄取率进行比较。利用生长曲线和琼脂平皿记数法,观察转化试剂和(或)转化方法对细菌增殖能力的影响。结果:So-fastTM转化组的摄取率最高,近80%,其次为电穿孔组(70.5%)和脂质体转化组(17.3%),自然转化组的摄取率最低,约4%。So-fastTM组和对照组的菌落计数和生长曲线均无明显差别(P>0.05),电穿孔组与未穿孔组的菌落计数差别明显(P<0.01)。结论:So-fastTM有明显的促转化作用,并且不影响受试菌的增殖,可做为寡核苷酸转化变形链球菌的载体。Objective: To screen out an appropriate delivery system for transformation of Streptococcus mutans with antisense phosphorothioate oligodeoxyribonucleotides (PS-ODN) to regulate gene expressions. Methods: To delivery FITC labeled PS-ODN into S. mutans using polycation So-fast^TM and cationic liposomes lipofectamine2000 as transfer carrier; natural transformation and electroporation was also applied; the uptake rate was recorded by FACS. The effects of various treatments on viability and recovery of S. mutans were determined by growth curve and colony number counting. Results: The largest uptake rate was achieved by the combination of FITC-labeled PS-ODN with So-fast^TM, in which about 80% of bacterial cells had integrated antisense oligonucleotides, followed by electroproation(70.5% ) , encapsulated PS-ODN with lipofectamine2000( 17.3% ) and free PS-ODN(4% ). The results of growth curve and cloneforming units (CFU) counting showed that So-fast^TM had no significant effects on proliferation and recovery of S. mutans ( P 〉 0.05 ). Conclusion : So-fast^TM can greatly improve the penetration of PS-ODN into S. mutans and can be used as appropriate delivery system of PS-ODN for S. mutans. No matter what approaches were adopted, the uptake rate reached the maximum at 5 μmol/L and 2 h-exposure. The penetration can not be enhanced by increasing the PS-ODN concentration and the transformation time.
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