Park YongKeun, Diez-Silva Monica, Popescu Gabriel, Lykotrafitis George, Choi Wonshik, Feld Michael S, Suresh Subra
G. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2008 Sep 16;105(37):13730-5. doi: 10.1073/pnas.0806100105. Epub 2008 Sep 4.
Parasitization by malaria-inducing Plasmodium falciparum leads to structural, biochemical, and mechanical modifications to the host red blood cells (RBCs). To study these modifications, we investigate two intrinsic indicators: the refractive index and membrane fluctuations in P. falciparum-invaded human RBCs (Pf-RBCs). We report experimental connections between these intrinsic indicators and pathological states. By employing two noninvasive optical techniques, tomographic phase microscopy and diffraction phase microscopy, we extract three-dimensional maps of refractive index and nanoscale cell membrane fluctuations in isolated RBCs. Our systematic experiments cover all intraerythrocytic stages of parasite development under physiological and febrile temperatures. These findings offer potential, and sufficiently general, avenues for identifying, through cell membrane dynamics, pathological states that cause or accompany human diseases.
由导致疟疾的恶性疟原虫寄生会使宿主红细胞(RBCs)发生结构、生化和机械变化。为了研究这些变化,我们研究了两个内在指标:恶性疟原虫感染的人类红细胞(Pf-RBCs)的折射率和膜波动。我们报告了这些内在指标与病理状态之间的实验联系。通过使用两种非侵入性光学技术,断层相显微镜和衍射相显微镜,我们提取了分离红细胞中折射率和纳米级细胞膜波动的三维图。我们的系统实验涵盖了寄生虫在生理和发热温度下发育的所有红细胞内阶段。这些发现为通过细胞膜动力学识别导致或伴随人类疾病的病理状态提供了潜在且足够通用的途径。