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Understanding the significance of oxygen tension on the biology of Plasmodium falciparum blood stages: From the human body to the laboratory

机译:了解氧张力对恶性疟原虫血液分期生物学的影响:从人体到实验室

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摘要

Plasmodium falciparum undergoes sequestration within deep tissues of the human body, spanning multiple organ systems with differing oxygen (O2) concentrations. The parasite is exposed to an even greater range of O2 concentrations as it transitions from the human to the mosquito host, suggesting a high level of plasticity as it navigates these different environments. In this review, we explore factors that may contribute to the parasite’s response to different environmental O2 concentrations, recognizing that there are likely multiple pieces to this puzzle. We first review O2-sensing mechanisms, which exist in other apicomplexans such as Toxoplasma gondii and consider whether similar systems could exist in Plasmodium. Next, we review morphological and functional changes in P. falciparum’s mitochondrion during the asexual-to-sexual stage transition and discuss how these changes overlap with the parasite’s access to O2. We then delve into reactive oxygen species (ROS) as ROS production is influenced by O2 availability and oxidative stress impacts Plasmodium intraerythrocytic development. Lastly, given that the primary role of the red blood cell (RBC) is to deliver O2 throughout the body, we discuss how changes in the oxygenation status of hemoglobin, the RBC’s O2-carrying protein and key nutrient for Plasmodium, could also potentially impact the parasite’s growth during intraerythrocytic development. This review also highlights studies that have investigated P. falciparum biology under varying O2 concentrations and covers technical aspects related to P. falciparum cultivation in the lab, focusing on sources of technical variation that could alter the amount of dissolved O2 encountered by cells during in vitro experiments. Lastly, we discuss how culture systems can better replicate in vivo heterogeneity with respect to O2 gradients, propose ideas for further research in this area, and consider translational implications related to O2 and malaria.
机译:恶性疟原虫在人体深层组织内进行隔离,跨越具有不同氧气 (O2) 浓度的多个器官系统。当寄生虫从人类转变为蚊子宿主时,它会暴露在更大范围的 O2 浓度下,这表明它在驾驭这些不同的环境时具有高度的可塑性。在这篇综述中,我们探讨了可能导致寄生虫对不同环境 O2 浓度做出反应的因素,认识到这个难题可能有多个部分。我们首先回顾了存在于其他顶复体(如刚地弓形虫)中的 O 2 感应机制,并考虑疟原虫中是否存在类似的系统。接下来,我们回顾了恶性疟原虫线粒体在无性到有性阶段过渡期间的形态和功能变化,并讨论了这些变化如何与寄生虫获得 O2 重叠。然后,我们深入研究活性氧 (ROS),因为 ROS 的产生受 O 2 可用性的影响,而氧化应激会影响疟原虫红细胞内的发育。最后,鉴于红细胞 (RBC) 的主要作用是将 O2 输送到全身,我们讨论了血红蛋白(RBC 的 O2 携带蛋白和疟原虫的关键营养素)的氧合状态的变化如何也可能影响寄生虫在红细胞内发育过程中的生长。本综述还重点介绍了调查 P 的研究。不同 O 2 浓度下的恶性疟原虫生物学,涵盖与实验室中恶性疟原虫培养相关的技术方面,重点关注可能改变细胞在体外实验期间遇到的溶解 O 2 量的技术变异来源。最后,我们讨论了培养系统如何更好地复制 O 2 梯度方面的体内异质性,提出了该领域进一步研究的想法,并考虑了与 O 2 和疟疾相关的转化影响。

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