Division of Medical Zoology, Department of Infection and Immunity, Jichi Medical University, Tochigi, Japan.
Nanostructure Characterization Group, Solution Development Department, Hitachi High-Tech Corporation, Tokyo, Japan.
Front Cell Infect Microbiol. 2022 Aug 22;12:962495. doi: 10.3389/fcimb.2022.962495. eCollection 2022.
gametocytes have unique morphology, metabolism, and protein expression profiles in their asexual stages of development. In addition to the striking changes in their appearance, a wide variety of "exo-membrane structures" are newly formed in the gametocyte stage. Little is known about their function, localization, or three-dimensional structural information, and only some structural data, typically two-dimensional, have been reported using conventional electron microscopy or fluorescence microscopy. For better visualization of intracellular organelle and exo-membrane structures, we previously established an unroofing technique to directly observe Maurer's clefts (MCs) in asexual parasitized erythrocytes by removing the top part of the cell's membrane followed by transmission electron microscopy. We found that MCs have numerous tethers connecting themselves to the host erythrocyte membrane skeletons. In this study, we investigated the intracellular structures of gametocytes using unroofing-TEM, Serial Block Face scanning electron microscopy, and fluorescence microscopy to unveil the exo-membrane structures in gametocytes. Our data showed "balloon/pouch"-like objects budding from the parasitophorous vacuole membrane (PVM) in gametocytes, and some balloons included multiple layers of other balloons. Furthermore, numerous bubbles appeared on the inner surface of the erythrocyte membrane or PVM; these were similar to MC-like membranes but were smaller than asexual MCs. Our study demonstrated reforms exo-membranes in erythrocytes to meet stage-specific biological activities during their sexual development.
配子在无性发育阶段具有独特的形态、代谢和蛋白表达谱。除了外观的显著变化外,在配子阶段还会新形成各种各样的“外膜结构”。这些结构的功能、定位或三维结构信息知之甚少,仅报道了一些使用传统电子显微镜或荧光显微镜获得的结构数据,通常为二维数据。为了更好地观察细胞内细胞器和外膜结构,我们之前建立了一种去顶技术,通过去除细胞膜的顶部部分,直接观察无性寄生红细胞中的 Maurer 氏裂隙(MCs),然后进行透射电子显微镜观察。我们发现 MCs 有许多系绳将自身连接到宿主红细胞膜骨架上。在这项研究中,我们使用去顶 TEM、连续块面扫描电子显微镜和荧光显微镜研究配子的细胞内结构,以揭示配子中的外膜结构。我们的数据显示,配子中的滋养体空泡膜(PVM)上有“气球/囊泡”样物体出芽,一些气球内包含多层其他气球。此外,在红细胞膜或 PVM 的内表面上出现了许多气泡;这些类似于 MC 样膜,但比无性 MC 小。我们的研究表明,在有性发育过程中,红细胞会重塑外膜以适应特定阶段的生物活性。