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覃金红, 彭延, 董惠芬, 蒋明森, 明珍平, 钟沁萍. 肝基质与/或β-巯基乙醇对日本血吸虫细胞影响[J]. 中国公共卫生, 2005, 21(10): 1182-1183.
引用本文: 覃金红, 彭延, 董惠芬, 蒋明森, 明珍平, 钟沁萍. 肝基质与/或β-巯基乙醇对日本血吸虫细胞影响[J]. 中国公共卫生, 2005, 21(10): 1182-1183.
QIN Jinhong, PENG Yan, DONG Huifen, . Effects of liver matrix or/and β-Mercaptoethanol on cultured cells from Schistosoma japonicum[J]. Chinese Journal of Public Health, 2005, 21(10): 1182-1183.
Citation: QIN Jinhong, PENG Yan, DONG Huifen, . Effects of liver matrix or/and β-Mercaptoethanol on cultured cells from Schistosoma japonicum[J]. Chinese Journal of Public Health, 2005, 21(10): 1182-1183.

肝基质与/或β-巯基乙醇对日本血吸虫细胞影响

Effects of liver matrix or/and β-Mercaptoethanol on cultured cells from Schistosoma japonicum

  • 摘要:
      目的   研究肝基质与β-巯基乙醇分别及联合作用对日本血吸虫培养细胞的影响。
      方法   冷消化法将虫龄为18 d的日本血吸虫童虫制成细胞悬液, 联合法接种于普通小盖玻片和预先铺敷肝基质的小盖玻片上。前者被随机分为对照组与β-巯基乙醇组, 后者被分为肝基质组与β-巯基乙醇+肝基质联合处理组(简称联合组)。培养第1~4周, 分别对各组细胞进行乳酸脱氢酶(LDH)染色, 光镜下观察分析。
      结果   培养第1周细胞的LDH活性最强; 随着培养时间的延长, LDH活性逐渐降低。培养前2周, β-巯基乙醇组与联合组细胞的LDH活性相近, 肝基质组与对照组的相近, 前者强于后者, 差异有统计学意义(P < 0.05)。培养第3周始, 肝基质组培养细胞的LDH活性最强, 与其余组比较, 差异有统计学意义(P < 0.05);其余组之间两两比较, 差异无统计学意义(P > 0.05)。
      结论   肝基质对日本血吸虫培养细胞LDH活性的促进作用比β-巯基乙醇稳定、长效; 两者联合无协同作用。

     

    Abstract:
      Objective   To study the effects of the liver matrix(bio-matrix from the liver of a rabbit)or/and β-M ercaptoethanol (β-Me)on the cultured cells from Schistosoma japonicum.
      Methods   After schistosomula cells from 18-day old S. japonicum were prepared by a method of cold digestion, they were inoculated with the method of combination on general glass coverslips or the glass coverslips smeared with the liver matrix. The former was divided in to control andβ-Me groups, the later was liver matrix and combination(of β-Me and liver matrix)groups randomly. The cells in the control and liver matrix groups were cultured in the routine media, i.e., medium RPMI-1640 containing 20% calf serum and a moderate amount of antibiotics(penicillin G 100 iu/ml, streptomycin 100 μg/ml), while those in β-Me and combination groups were cultured in the routine media containing 50 μmol/L β-Me and l mmol/L sodium pyruvate. When cultured for 1, 2, 3 and 4 weeks, the cells were stained to show the activities of lactatedehydrogenase(LDH) by using the cytochemical method of enzyme, respectively. They were observed and photographed by the microscope(Olympus-BH2). The activities of LDH were measured by using the photomete-rimage analytical instrument(HPIA-2000)and analyzed statistically.
      Results   The activities of LDH were the strongest in the cells from S. japonicumcultured for 1 week. Along with prolongation of the culture time, the activities of LDH became weaker gradually. In the first two weeks, the activities of LDH in the cells in β-Me group were similar to those in the combination group, and the group of the liver matrix similar to the control but weaker than the above groups. Quantitative analysis showed that the difference of LDH concentration in the cultured cells between β-Me, combination groups and the liver matrix, control groups was significant(P < 0.05). Three weeks later, the activities of LDH in the ceils of the liver matrix group were stronger than those in β-Me, combination and control groups, and the difference was significant(P < 0.05). However, no significant difference among the latter 3 groups were observe(P > 0.05).
      Conclusion   The effects of the liver matrix on the activities of LDH in the cultured cells from S. japonicum were probably more effective and steady-going than those of β-Me. The enhanced effects of the liver matrix plus β-Me on the cultured cells was not observed in the study.

     

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