Song Hyun-Ouk, Ahn Myoung-Hee, Ryu Jae-Sook, Min Duk-Young, Joo Kyoung-Hwan, Lee Young-Ha
Department of Parasitology and Institute of Biomedical Science, Hanyang University College of Medicine, Seoul 133-791, Korea.
Korean J Parasitol. 2004 Dec;42(4):185-93. doi: 10.3347/kjp.2004.42.4.185.
Toxoplasma gondii is an obligate intracellular protozoan parasite, which invades a wide range of hosts including humans. The exact mechanisms involved in its invasion are not fully understood. This study focused on the roles of Ca2+ in host cell invasion and in T. gondii replication. We examined the invasion and replication of T. gondii pretreated with several calcium modulators, the conoid extrusion of tachyzoites. Calmodulin localization in T. gondii were observed using the immunogold method, and Ca2+ levels in tachyzoites by confocal microscopy. In light microscopic observation, tachyzoites co-treated with A23187 and EGTA showed that host cell invasion and intracellular replication were decreased. The invasion of tachyzoites was slightly inhibited by the Ca2+ channel blockers, bepridil and verapamil, and by the calmodulin antagonist, calmidazolium. We observed that calcium saline containing A23187 induced the extrusion of tachyzoite conoid. By immunoelectron microscopy, gold particles bound to anti-calmodulin or anti-actin mAb, were found to be localized on the anterior portion of tachyzoites. Remarkably reduced intracellular Ca2+ was observed in tachyzoites treated with BAPTA/AM by confocal microscopy. These results suggest that host cell invasion and the intracellular replication of T. gondii tachyzoites are inhibited by the calcium ionophore, A23187, and by the extracellular calcium chelator, EGTA.
刚地弓形虫是一种专性细胞内原生动物寄生虫,可侵入包括人类在内的多种宿主。其侵入所涉及的确切机制尚未完全明确。本研究聚焦于Ca2+在宿主细胞侵入及刚地弓形虫复制中的作用。我们检测了用几种钙调节剂预处理后的刚地弓形虫的侵入和复制情况,以及速殖子的类锥体挤出情况。采用免疫金法观察钙调蛋白在刚地弓形虫中的定位,并用共聚焦显微镜检测速殖子中的Ca2+水平。在光学显微镜观察中,与A23187和乙二醇双四乙酸(EGTA)共同处理的速殖子显示宿主细胞侵入和细胞内复制减少。Ca2+通道阻滞剂苄普地尔和维拉帕米以及钙调蛋白拮抗剂氯咪唑可轻微抑制速殖子的侵入。我们观察到含A23187的钙盐可诱导速殖子类锥体挤出。通过免疫电子显微镜观察,发现与抗钙调蛋白或抗肌动蛋白单克隆抗体结合的金颗粒定位于速殖子的前部。用共聚焦显微镜观察发现,用1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸/乙酰甲酯(BAPTA/AM)处理的速殖子细胞内Ca2+显著降低。这些结果表明,钙离子载体A23187和细胞外钙螯合剂EGTA可抑制刚地弓形虫速殖子的宿主细胞侵入和细胞内复制。