Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge, United Kingdom.
Biophys J. 2011 Mar 16;100(6):1438-45. doi: 10.1016/j.bpj.2011.02.007.
Plasmodium falciparum is responsible for severe malaria. During the ∼48 h duration of its asexual reproduction cycle in human red blood cells, the parasite causes profound alterations in the homeostasis of the host red cell, with reversal of the normal Na and K gradients across the host cell membrane, and a drastic fall in hemoglobin content. A question critical to our understanding of how the host cell retains its integrity for the duration of the cycle had been previously addressed by modeling the homeostasis of infected cells. The model predicted a critical contribution of excess hemoglobin consumption to cell integrity (the colloidosmotic hypothesis). Here we tested this prediction with the use of electron-probe x-ray microanalysis to measure the stage-related changes in Na, K, and Fe contents in single infected red cells and in uninfected controls. The results document a decrease in Fe signal with increased Na/K ratio. Interpreted in terms of concentrations, the results point to a sustained fall in host cell hemoglobin concentration with parasite maturation, supporting a colloidosmotic role of excess hemoglobin digestion. The results also provide, for the first time to our knowledge, comprehensive maps of the elemental distributions of Na, K, and Fe in falciparum-infected red blood cells.
恶性疟原虫是导致严重疟疾的罪魁祸首。在其在人体红细胞中的无性繁殖周期的 48 小时内,寄生虫导致宿主红细胞的内稳态发生深刻变化,导致宿主细胞膜上正常的 Na 和 K 梯度逆转,血红蛋白含量急剧下降。之前,通过对受感染细胞的内稳态进行建模,解决了一个对我们理解宿主细胞如何在整个周期内保持完整性至关重要的问题。该模型预测,过量血红蛋白的消耗对细胞完整性有重要贡献(胶体渗透压假说)。在这里,我们使用电子探针 X 射线微分析来测量单个受感染的红细胞和未受感染的对照中的 Na、K 和 Fe 含量的阶段相关变化,从而验证了这一预测。结果记录了 Fe 信号随 Na/K 比值的增加而降低。根据浓度来解释,这些结果表明随着寄生虫的成熟,宿主细胞血红蛋白浓度持续下降,支持过量血红蛋白消化的胶体渗透压作用。这些结果还首次提供了我们所知的恶性疟原虫感染的红细胞中 Na、K 和 Fe 的元素分布的全面图谱。