拟南芥产生不同的细胞外囊泡亚群,对生物胁迫有不同的反应,改变真菌病原体的生长和感染性

IF 14.5 1区 医学 Q1 CELL BIOLOGY
Benjamin L. Koch, Brian D. Rutter, M. Lucía Borniego, Meenu Singla-Rastogi, Dillon M. Gardner, Roger W. Innes
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引用次数: 0

摘要

哺乳动物细胞分泌的细胞外囊泡(EVs)在内容和功能上具有高度的异质性。植物细胞分泌的电动汽车是否也是如此尚不清楚。为了解决这个问题,我们使用高分辨率密度梯度超离心和全内部荧光显微镜(TIRF-M)来纯化和区分不同的拟南芥ev亚群。在中密度EV中特异检测到EV标记蛋白TET8。利用TIRF-M证实TET8和穿透1 (PEN1)在大多数单独的EV群体中分泌,而PEN1与穿透3 (PEN3)共同分泌的频率更高。以TET8、PEN1和rpm1相互作用蛋白4 (RIN4)为标志的EV亚群在植物激素、温度变化和真菌病原体感染的诱导下分泌到外质体和叶表面。植物EVs处理拟南芥幼苗通过改变真菌胚管发育和真菌形态来延缓真菌感染的进展。值得注意的是,细胞外rna,包括mirna和sirna,没有与tet8标记的ev共分离,而是与高密度馏分中的囊外ARGONAUTE蛋白共分离。总之,这些数据表明拟南芥EVs具有高度异质性,有助于免疫,但不太可能介导跨界RNA干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Arabidopsis Produces Distinct Subpopulations of Extracellular Vesicles That Respond Differentially to Biotic Stress, Altering Growth and Infectivity of a Fungal Pathogen

Arabidopsis Produces Distinct Subpopulations of Extracellular Vesicles That Respond Differentially to Biotic Stress, Altering Growth and Infectivity of a Fungal Pathogen

Extracellular vesicles (EVs) secreted by mammalian cells are highly heterogeneous in content and function. Whether this is also true for EVs secreted by plant cells is not yet known. To address this, we used high-resolution density gradient ultracentrifugation and total internal fluorescence microscopy (TIRF-M) to purify and distinguish distinct subpopulations of Arabidopsis EVs. The EV marker protein TETRASPANIN 8 (TET8) was detected specifically in medium-density EVs. TET8 and PENETRATION 1 (PEN1) were confirmed to be secreted in mostly separate EV populations using TIRF-M, while PEN1 was co-secreted with PENETRATION 3 (PEN3) much more often. Secretion of EV subpopulations marked by TET8, PEN1 and RPM1-INTERACTING PROTEIN 4 (RIN4) into the apoplast and onto the leaf surface was induced by phytohormones, changes in temperature and infection with fungal pathogens. Treatment of Arabidopsis seedlings with plant EVs delayed the progression of fungal infection by altering fungal germ tube development and fungal morphology. Significantly, extracellular RNAs, including miRNAs and siRNAs, did not co-fractionate with TET8-labeled EVs, and instead, co-fractionated with extravesicular ARGONAUTE proteins in high-density fractions. Together, these data indicate that Arabidopsis EVs are highly heterogeneous and contribute to immunity but are unlikely to mediate cross-kingdom RNA interference.

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来源期刊
Journal of Extracellular Vesicles
Journal of Extracellular Vesicles Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
27.30
自引率
4.40%
发文量
115
审稿时长
12 weeks
期刊介绍: The Journal of Extracellular Vesicles is an open access research publication that focuses on extracellular vesicles, including microvesicles, exosomes, ectosomes, and apoptotic bodies. It serves as the official journal of the International Society for Extracellular Vesicles and aims to facilitate the exchange of data, ideas, and information pertaining to the chemistry, biology, and applications of extracellular vesicles. The journal covers various aspects such as the cellular and molecular mechanisms of extracellular vesicles biogenesis, technological advancements in their isolation, quantification, and characterization, the role and function of extracellular vesicles in biology, stem cell-derived extracellular vesicles and their biology, as well as the application of extracellular vesicles for pharmacological, immunological, or genetic therapies. The Journal of Extracellular Vesicles is widely recognized and indexed by numerous services, including Biological Abstracts, BIOSIS Previews, Chemical Abstracts Service (CAS), Current Contents/Life Sciences, Directory of Open Access Journals (DOAJ), Journal Citation Reports/Science Edition, Google Scholar, ProQuest Natural Science Collection, ProQuest SciTech Collection, SciTech Premium Collection, PubMed Central/PubMed, Science Citation Index Expanded, ScienceOpen, and Scopus.
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