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首页> 外文期刊>PLoS Pathogens >Disruption of Toxoplasma gondii Parasitophorous Vacuoles by the Mouse p47-Resistance GTPases
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Disruption of Toxoplasma gondii Parasitophorous Vacuoles by the Mouse p47-Resistance GTPases

机译:小鼠p47-抗性GTPases破坏弓形虫的寄生虫液泡。

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摘要

The p47 GTPases are essential for interferon-γ-induced cell-autonomous immunity against the protozoan parasite, Toxoplasma gondii, in mice, but the mechanism of resistance is poorly understood. We show that the p47 GTPases, including IIGP1, accumulate at vacuoles containing T. gondii. The accumulation is GTP-dependent and requires live parasites. Vacuolar IIGP1 accumulations undergo a maturation-like process accompanied by vesiculation of the parasitophorous vacuole membrane. This culminates in disruption of the parasitophorous vacuole and finally of the parasite itself. Over-expression of IIGP1 leads to accelerated vacuolar disruption whereas a dominant negative form of IIGP1 interferes with interferon-γ-mediated killing of intracellular parasites. Targeted deletion of the IIGP1 gene results in partial loss of the IFN-γ-mediated T. gondii growth restriction in mouse astrocytes.
机译:p47 GTPases对于干扰素-γ诱导的小鼠抗原生动物寄生虫弓形虫的细胞自主免疫至关重要,但耐药机制尚不清楚。我们显示p47 GTPases,包括IIGP1,积累在含有弓形虫的液泡中。积累是GTP依赖的,并且需要活寄生虫。液泡IIGP1积累经历了类似成熟的过程,并伴有寄生虫的液泡膜囊泡化。这最终导致了寄生虫空泡的破坏,最后是寄生虫本身的破坏。 IIGP1的过度表达导致液泡破裂加速,而IIGP1的显性负性形式则干扰了干扰素-γ介导的细胞内寄生虫的杀伤。 IIGP1基因的靶向删除导致小鼠星形胶质细胞中IFN-γ介导的弓形虫生长限制的部分丧失。

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