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Small Variant STEVOR Antigen Is Uniquely Located within Maurer's Clefts in Plasmodium falciparum-Infected Red Blood Cells

机译:小变异STEVOR抗原独特地位于恶性疟原虫感染的红细胞中的毛拉尔裂隙内

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Malaria parasite antigens encoded by multigene families are important factors in virulence and in disease pathology. In Plasmodium falciparum, the virulence factor PfEMP-1 is encoded by the var multigene family and is exposed at the infected erythrocyte surface. PfEMP-1 is clonally variant, allowing the parasite to evade host immunity. The recently identified P. falciparum stevor multigene family and its products also have the potential to be involved in similar important aspects of host-parasite interactions. Here, we show tightly regulated stage-specific transcription of stevor occurring over just a few hours of the asexual parasite life cycle. Only a subset of stevor genes are transcribed in parasite populations maintained in cultures and in single micromanipulated parasites. Antibodies against STEVOR recognize proteins of the expected size (~37 kDa) and localize STEVOR in Maurer's clefts, unique membranous structures located in the cytoplasm of infected erythrocytes. The fact that the timing of stevor expression and the location of STEVOR are clearly distinct from those of other parasite variant antigens suggests that this gene family may have a novel role in P. falciparum biology.
机译:多基因家族编码的疟原虫抗原是毒力和疾病病理学的重要因素。在恶性疟原虫中,毒力因子PfEMP-1由 var 多基因家族编码,并暴露于受感染的红细胞表面。 PfEMP-1是克隆变异体,允许该寄生虫逃避宿主免疫力。最近确定的 P。恶性疟原虫多基因家族及其产品也可能参与宿主-寄生虫相互作用的类似重要方面。在这里,我们显示了在无性寄生虫生命周期的仅几个小时内发生的,严格调控的 stevor 阶段特异性转录。只是 stevor 基因的一个子集在维持在培养物中的寄生虫种群和单个微操纵的寄生虫中转录。抗STEVOR的抗体可识别预期大小(〜37 kDa)的蛋白质,并将STEVOR定位在毛勒氏裂隙中,毛利氏裂隙位于感染的红细胞细胞质中,是独特的膜状结构。 stevor 的表达时间和STEVOR的位置与其他寄生虫变异抗原明显不同,这一事实表明该基因家族可能在 P中具有新的作用。恶性肿瘤生物学。

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