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Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles

机译:低温微粒的低温透射电镜纳米结构研究

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摘要

Microparticles (MPs) are sub-micron membrane vesicles (100–1000 nm) shed from normal and pathologic cells due to stimulation or apoptosis. MPs can be found in the peripheral blood circulation of healthy individuals, whereas elevated concentrations are found in pregnancy and in a variety of diseases. Also, MPs participate in physiological processes, e.g., coagulation, inflammation, and angiogenesis. Since their clinical properties are important, we have developed a new methodology based on nano-imaging that provides significant new data on MPs nanostructure, their composition and function. We are among the first to characterize by direct-imaging cryogenic transmitting electron microscopy (cryo-TEM) the near-to-native nanostructure of MP systems isolated from different cell types and stimulation procedures. We found that there are no major differences between the MP systems we have studied, as most particles were spherical, with diameters from 200 to 400 nm. However, each MP population is very heterogeneous, showing diverse morphologies. We investigated by cryo-TEM the effects of standard techniques used to isolate and store MPs, and found that either high-g centrifugation of MPs for isolation purposes, or slow freezing to –80°C for storage introduce morphological artifacts, which can influence MP nanostructure, and thus affect the efficiency of these particles as future diagnostic tools.
机译:微粒(MPs)是由于刺激或凋亡而从正常和病理细胞中脱落的亚微米级膜囊泡(100-1000 nm)。可以在健康人的外周血中发现MP,而在怀孕和各种疾病中发现MP升高。而且,MP参与生理过程,例如凝血,炎症和血管生成。由于它们的临床特性很重要,因此我们开发了一种基于纳米成像的新方法,该方法提供了有关MP纳米结构,其组成和功能的重要新数据。我们是第一个通过直接成像低温透射电子显微镜(cryo-TEM)表征从不同细胞类型和刺激程序中分离出来的MP系统的接近自然的纳米结构的人。我们发现,我们研究的MP系统之间没有主要区别,因为大多数粒子是球形的,直径从200到400 nm。但是,每个MP种群非常异质,表现出多种形态。我们通过冷冻TEM研究了用于分离和存储MP的标准技术的效果,发现用于分离目的MP的高g离心或用于存储的缓慢冷冻至–80°C都会引入形态学假象,从而影响MP纳米结构,从而影响这些颗粒作为未来诊断工具的效率。

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