Makioka Asao, Kumagai Masahiro, Kobayashi Seiki, Takeuchi Tsutomu
Department of Tropical Medicine, Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato-ku, Tokyo 105-8461, Japan.
Exp Parasitol. 2003 Jan-Feb;103(1-2):61-7. doi: 10.1016/s0014-4894(03)00073-0.
The effect of aphidicolin, a specific inhibitor of the replicative DNA polymerases, on the excystation and metacystic development of Entamoeba invadens was examined. The protein profile of metacystic amoebae and their immunogenicity in the presence and absence of aphidicolin were also examined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting. Excystation, which was assessed by counting the number of metacystic amoebae after the induction of excystation, was inhibited by aphidicolin in a concentration-dependent manner during incubation compared to the controls. Metacystic development, when determined by the number of nuclei in amoeba, was also inhibited by aphidicolin, because the percentage of 4-nucleate amoebae in cultures with aphidicolin during incubation was higher than that in cultures without the drug. The addition of aphidicolin to cultures at day 1 of incubation reduced the number of metacystic amoebae thereafter compared to cultures without the drug. The inhibitory effect of aphidicolin on excystation and metacystic development was reversed by removal of the drug. Pretreatment of cysts with aphidicolin before transfer to a growth medium containing the drug had no further effect on the excystation and metacystic development. Cellular proteins of metacystic amoebae with 4 nuclei, which were predominant even at day 3 in the cultures with aphidicolin, reacted strongly with rabbit anticyst serum absorbed with trophozoite proteins. In contrast, those of metacystic amoebae with 1 nucleus, which were predominant at day 3 in cultures without aphidicolin, no longer reacted with the absorbed anticyst serum, suggesting change in the expression of proteins during metacystic development.
研究了复制性DNA聚合酶的特异性抑制剂阿非科林对侵袭内阿米巴脱囊和包囊后发育的影响。还通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和免疫印迹法检测了在有或没有阿非科林存在的情况下包囊后阿米巴的蛋白质谱及其免疫原性。与对照相比,在孵育期间,通过计数脱囊诱导后包囊后阿米巴的数量来评估的脱囊受到阿非科林的浓度依赖性抑制。当通过阿米巴细胞核的数量来确定时,包囊后发育也受到阿非科林的抑制,因为在孵育期间含有阿非科林的培养物中四核阿米巴的百分比高于没有该药物的培养物。在孵育第1天向培养物中添加阿非科林,与没有该药物的培养物相比,此后包囊后阿米巴的数量减少。去除药物后,阿非科林对脱囊和包囊后发育的抑制作用得以逆转。在转移到含有该药物的生长培养基之前,用阿非科林对包囊进行预处理对脱囊和包囊后发育没有进一步影响。即使在含有阿非科林的培养物中第3天仍占主导地位的四核包囊后阿米巴的细胞蛋白,与用滋养体蛋白吸收的兔抗包囊血清发生强烈反应。相比之下,在没有阿非科林的培养物中第3天占主导地位的单核包囊后阿米巴的细胞蛋白不再与吸收后的抗包囊血清发生反应,这表明在包囊后发育过程中蛋白质表达发生了变化。