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食脑变形虫多种临床分离株的细胞外囊泡特征、超微结构形态及细胞间相互作用

Characterization of the extracellular vesicles, ultrastructural morphology, and intercellular interactions of multiple clinical isolates of the brain-eating amoeba, .

作者信息

Russell A Cassiopeia, Bush Peter, Grigorean Gabriela, Kyle Dennis E

机构信息

Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA, United States.

Department of Infectious Diseases, University of Georgia, Athens, GA, United States.

出版信息

Front Microbiol. 2023 Sep 27;14:1264348. doi: 10.3389/fmicb.2023.1264348. eCollection 2023.

DOI:10.3389/fmicb.2023.1264348
PMID:37808283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10558758/
Abstract

INTRODUCTION

As global temperatures rise to unprecedented historic levels, so too do the latitudes of habitable niches for the pathogenic free-living amoeba, . This opportunistic parasite causes a rare, but >97% fatal, neurological infection called primary amoebic meningoencephalitis. Despite its lethality, this parasite remains one of the most neglected and understudied parasitic protozoans.

METHODS

To better understand amoeboid intercellular communication, we elucidate the structure, proteome, and potential secretion mechanisms of amoeba-derived extracellular vesicles (EVs), which are membrane-bound communication apparatuses that relay messages and can be used as biomarkers for diagnostics in various diseases.

RESULTS AND DISCUSSION

Herein we propose that secretes EVs in clusters from the plasma membrane, from multivesicular bodies, and via beading of thin filaments extruding from the membrane. Uptake assays demonstrate that EVs are taken up by other amoebae and mammalian cells, and we observed a real-time increase in metabolic activity for mammalian cells exposed to EVs from amoebae. Proteomic analysis revealed >2,000 proteins within the -secreted EVs, providing targets for the development of diagnostics or therapeutics. Our work expands the knowledge of intercellular interactions among these amoebae and subsequently deepens the understanding of the mechanistic basis of PAM.

摘要

引言

随着全球气温升至前所未有的历史水平,致病性自由生活变形虫的可居住生态位的纬度也在上升。这种机会性寄生虫会引发一种罕见但致死率超过97%的神经感染,称为原发性阿米巴脑膜脑炎。尽管其具有致命性,但这种寄生虫仍然是最被忽视和研究最少的寄生原生动物之一。

方法

为了更好地理解变形虫的细胞间通讯,我们阐明了变形虫衍生的细胞外囊泡(EVs)的结构、蛋白质组和潜在分泌机制,这些囊泡是传递信息的膜结合通讯装置,可作为各种疾病诊断的生物标志物。

结果与讨论

在此我们提出, 从质膜、多囊泡体以及通过从膜上挤出的细丝形成的珠状物以簇状分泌细胞外囊泡。摄取试验表明,细胞外囊泡被其他变形虫和哺乳动物细胞摄取,并且我们观察到暴露于来自变形虫的细胞外囊泡的哺乳动物细胞的代谢活性实时增加。蛋白质组学分析揭示了 分泌的细胞外囊泡中有超过2000种蛋白质,为诊断或治疗方法的开发提供了靶点。我们的工作扩展了对这些变形虫之间细胞间相互作用的认识,随后加深了对原发性阿米巴脑膜脑炎发病机制基础的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/b4d35738480f/fmicb-14-1264348-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/ca634e326e43/fmicb-14-1264348-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/1d57f3886f4e/fmicb-14-1264348-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/b7f999ce659a/fmicb-14-1264348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/b4d35738480f/fmicb-14-1264348-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/ca634e326e43/fmicb-14-1264348-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/618e05859c32/fmicb-14-1264348-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/dc42ffb9895c/fmicb-14-1264348-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/dd078f24fe08/fmicb-14-1264348-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/1d57f3886f4e/fmicb-14-1264348-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/b7f999ce659a/fmicb-14-1264348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e0/10558758/b4d35738480f/fmicb-14-1264348-g008.jpg

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