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明珍平, 钟沁萍, 董惠芬, 朱俊勇, 蒋明森. MNNG对日本血吸虫成虫培养细胞糖类物质作用[J]. 中国公共卫生, 2006, 22(1): 50-52. DOI: 10.11847/zgggws2006-22-01-27
引用本文: 明珍平, 钟沁萍, 董惠芬, 朱俊勇, 蒋明森. MNNG对日本血吸虫成虫培养细胞糖类物质作用[J]. 中国公共卫生, 2006, 22(1): 50-52. DOI: 10.11847/zgggws2006-22-01-27
MING Zhenping, ZHONG Qinping, DONG Huifen, . Effects of N-Methyl-N-Nitro-N-Nitrosoguanidine on carbohydrate in cultured cells from adult Schistosoma japanicum[J]. Chinese Journal of Public Health, 2006, 22(1): 50-52. DOI: 10.11847/zgggws2006-22-01-27
Citation: MING Zhenping, ZHONG Qinping, DONG Huifen, . Effects of N-Methyl-N-Nitro-N-Nitrosoguanidine on carbohydrate in cultured cells from adult Schistosoma japanicum[J]. Chinese Journal of Public Health, 2006, 22(1): 50-52. DOI: 10.11847/zgggws2006-22-01-27

MNNG对日本血吸虫成虫培养细胞糖类物质作用

Effects of N-Methyl-N-Nitro-N-Nitrosoguanidine on carbohydrate in cultured cells from adult Schistosoma japanicum

  • 摘要:
      目的   研究甲基硝基亚硝基胍(MNNG)对日本血吸虫成虫培养细胞糖类物质动态的影响.
      方法   将日本血吸虫成虫细胞接种于小盖玻片上, 置于RPMI-1640含20%小牛血清附加常量抗生素的常规培养基中培养.培养第4 d, 细胞被随机分为实验组和对照组.实验组细胞用含3μg/ml MNNG的常规培养基处理48 h, 对照组细胞用不含MNNG的常规培养基作相同处理.细胞经彻底清洗后, 继续以常规培养基培养3周, 然后换用含5%小牛血清的低血清培养基培养.NNNG处理后第1~8周, 每周取实验组和对照组细胞进行高碘酸雪夫(PAS)染色和淀粉酶处理后的PAS染色, 观察培养细胞内糖类物质的含量及分布变化.取培养第6周的染色细胞, 用HPIAS-2000图像分析仪测定细胞内代表糖含量的吸光度, 并作统计学分析.
      结果   随着培养时间的延长, 对照组培养细胞的着色逐渐变浅, 糖含量逐渐减少; 实验组细胞的着色则逐渐加深, 糖类物质和糖原含量均增加, 与对照组比较, 差异有统计学意义(P < 0.01).MNNG处理后第5周, 实验组细胞着色最深, 核质着色型第二类细胞和分裂细胞数目显著增加.
      结论   MNNG诱导后, 日本血吸虫成虫培养细胞内糖原和糖类物质含量均明显增加, 分裂细胞增多.

     

    Abstract:
      Objective   To study the dynamic effects of N-Methyl-N-Nitrosoguanidine(MN NG)on carbohy drate in the cultured cells from adult Schistosoma japanicum.
      Methods   The cultur ed cells from 32-day old S.japonicum were inoculated on cover slips and cultured in routine medium which was made up of RPMI-1640, 20% calf serum and moderate amount of antibiotics.At the 4th day, the cultured cells were div ided into test group and control group at random.The cells in the test group were treated with MNNG which final concentration in the routine medium was 3 μg/ml for 48 h, whereas those in the control group were treated with the routine medium free MNNG for the same time.After being washed tho roughly, they went on being cultured in the routine medium for 3 weeks; then were cultured in the low-serum medium which serum concentration was just 5%.From the 1st to 8th week, the cells were stained weekly to show the content and distribution of hepatin and carbo hydrate by Periodic A cid Scid Schiff reaction(PAS)and PAS staining after the cells were digested with amylase.The contents of carbohydrate in stained cells at the 6th week(the 5th week after inducement)were measured by using photometerimage analy tical instrument(HPIAS-2000)and analy zed by statistic method.
      Results   Along with the extending of the culture time, the staining of the cultured cells in the control group became weak, whereas those in the test group became strong.The contents of hepatin and carbohy drate of the cell in the test grop were significantly higher than those in the control group(P < 0.01).A the 6th week, not only the staining of the cells treated by MNNG were the deepest, but also the 2nd type cells and dividing cells incr eased significantly.
      Conclusion   MNNG could increase evidently the dividing cells and the content of hepatin and carbohydr ate in the cultured cells from adult S.japonicum.

     

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