发布: 2017年09月05日第7卷第17期 DOI: 10.21769/BioProtoc.2533 浏览次数: 20511
评审: Marisa RosaSibongile MafuAnonymous reviewer(s)
Abstract
Extracellular vesicles (EVs) play an important role in intercellular communication by transporting proteins and RNA. While plant cells secrete EVs, they have only recently been isolated and questions regarding their biogenesis, release, uptake and function remain unanswered. Here, we present a detailed protocol for isolating EVs from the apoplastic wash of Arabidopsis thaliana leaves. The isolated EVs can be quantified using a fluorometric dye to assess total membrane content.
Keywords: Arabidopsis thaliana (拟南芥)Background
Extracellular vesicles (EVs) are membrane-bound structures that mediate the cell-to-cell transfer of proteins, lipids and genetic material. Interest in mammalian EVs has grown over the years due to their ability to transfer RNA and modulate immune responses. Mammalian EVs are routinely isolated for study from the medium of cultured cells, as well as a growing list of biological fluids (Colombo et al., 2014). Plant EVs are also thought to have a role in the immune response but are comparatively understudied (An et al., 2007; Davis et al., 2016). This is due, in large part, to the absence of a method of isolation.
While plant EVs have been observed since 1967 using transmission electron microscopy, methods for their isolation were not developed until 2009 (Halperin and Jensen, 1967). Regente et al. (2009) isolated small (50-200 nm in diameter) vesicle-like structures from water-imbibed sunflower (Helianthus annuus) seeds. We modified the methods presented in Regente et al. (2009) to isolate vesicles from the apoplastic wash of Arabidopsis thaliana rosettes. To determine which conditions induce or impair EV secretion, we also designed a method for staining the EV pellet with 3,3’-dihexyloxacarbocyanine iodide (DIOC6(3)), a fluorescent lipophilic dye. In the absence of sophisticated forms of nanoparticle tracking, this relatively simple approach quantifies the total membrane content and can be used to indirectly measure the concentration of EVs (Rutter and Innes, 2017). For more precise measurements, and to assess the size distributions of EVs, nanoparticle tracking can be used. Our protocols enable the study of plant EV content and composition, as well as the pathways and conditions that mediate EV biogenesis and release.
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© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Readers should cite both the Bio-protocol article and the original research article where this protocol was used:
分类
植物科学 > 植物细胞生物学 > 细胞器分离
植物科学 > 植物细胞生物学 > 细胞间通讯
细胞生物学 > 细胞器分离 > 胞外囊泡
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