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首页> 外文期刊>Molecular biology of the cell >Stability and function of a putative microtubule-organizing center in the human parasite Toxoplasma gondii
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Stability and function of a putative microtubule-organizing center in the human parasite Toxoplasma gondii

机译:寄生虫毒素毒素毒素组织中心的稳定性和功能

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摘要

The organization of the microtubule cytoskeleton is dictated by microtubule nucleators or organizing centers. Toxoplasma gondii, an important human parasite, has an array of 22 regularly spaced cortical microtubules stemming from a hypothesized organizing center, the apical polar ring. Here we examine the functions of the apical polar ring by characterizing two of its components, KinesinA and APR1, and show that its putative role in templating can be separated from its mechanical stability. Parasites that lack both KinesinA and APR1 (Delta kinesinA Delta apr1) are capable of generating 22 cortical microtubules. However, the apical polar ring is fragmented in live Delta kinesinA Delta apr1 parasites and is undetectable by electron microscopy after detergent extraction. Disintegration of the apical polar ring results in the detachment of groups of microtubules from the apical end of the parasite. These structural defects are linked to a diminished ability of the parasite to move and invade host cells, as well as decreased secretion of effectors important for these processes. Together the findings demonstrate the importance of the structural integrity of the apical polar ring and the microtubule array in the Toxoplasma lytic cycle, which is responsible for massive tissue destruction in acute toxoplasmosis.
机译:微管细胞骨架的组织由微管核核心或组织中心决定。弓形虫,一种重要的人寄生虫,具有22个定期间隔的皮质微管,源于假设的组织中心,顶端极性环。在这里,我们通过表征其两个组件,kinesina和4月来检查顶端极性环的功能,并表明它在模板中的推定作用可以与其机械稳定性分开。缺乏Kinesina和Apr1(Delta Kinesina Delta APR1)的寄生虫能够产生22个皮质微管。然而,顶端极性环在活δKinesinadelta Apr1寄生虫中脱落,并且在洗涤剂萃取后通过电子显微镜可测义。顶端极性环的崩解导致从寄生虫的顶端脱离微管的分离。这些结构缺陷与寄生虫的减少能力与移动和侵入宿主细胞的减少相关联,以及对这些过程的效果分泌的分泌程度降低。调查结果表明了顶端极性环和弓形虫裂变循环中的微管阵列的结构完整性的重要性,这是急性毒素病中大规模组织破坏的原因。

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