光谱流式细胞术检测疟疾寄生虫来源的细胞外囊泡中的DNA货物。

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ewa Kozela, Ekaterina Petrovich-Kopitman, Yuval Berger, Abel Cruz Camacho, Yaara Shoham, Mattia I Morandi, Irit Rosenhek-Goldian, Ron Rotkopf, Neta Regev-Rudzki
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引用次数: 0

摘要

生物王国的细胞释放细胞外囊泡(EVs)作为与其他细胞交流的手段,无论它们是朋友还是敌人。细胞内疟原虫恶性疟原虫(Pf)确实如此,它利用ev将生物活性分子运送到各种人类宿主系统。然而,由于高分辨率工具的限制和缺乏商业抗体,疟疾研究中这种传播模式的研究目前受到限制。在这里,我们展示了一种先进的光谱流式细胞术方法的强大功能,可以强大地检测从pf感染的红细胞中分离出来的分泌ev。通过标记EV膜脂和DNA货物(非抗体染色方法),我们能够检测到富含DNA的寄生衍生EV亚群。此外,我们可以定量测量从寄生虫的两个不同血液阶段分离的携带dna的ev:环和滋养体。我们的研究结果显示了光谱流式细胞术监测致病性ev内核酸货物动态变化的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectral flow cytometry for detecting DNA cargo in malaria parasite-derived extracellular vesicles.

Cells across biological kingdoms release extracellular vesicles (EVs) as a means of communication with other cells, be their friends or foes. This is indeed true for the intracellular malaria parasite Plasmodium falciparum (Pf), which utilizes EVs to transport bioactive molecules to various human host systems. Yet, the study of this mode of communication in malaria research is currently constrained due to limitations in high-resolution tools and the absence of commercial antibodies. Here, we demonstrate the power of an advanced spectral flow cytometry approach to robustly detect secreted EVs, isolated from Pf-infected red blood cells. By labeling both EV membrane lipids and the DNA cargo within (non-antibody staining approach), we were able to detect a subpopulation of parasitic-derived EVs enriched in DNA. Furthermore, we could quantitatively measure the DNA-carrying EVs isolated from two distinct blood stages of the parasite: rings and trophozoites. Our findings showcase the potential of spectral flow cytometry to monitor dynamic changes in nucleic acid cargo within pathogenic EVs.

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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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