外源分子在细胞外囊泡形成前的光穿孔加载。

IF 12.6 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jana Ramon, Cláudio Pinheiro, Charysse Vandendriessche, Estefanía Lozano-Andrés, Herlinde De Keersmaecker, Deep Punj, Juan C Fraire, Edward Geeurickx, Marca H M Wauben, Pieter Vader, Roosmarijn E Vandenbroucke, An Hendrix, Stephan Stremersch, Stefaan C De Smedt, Koen Raemdonck, Kevin Braeckmans
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引用次数: 0

摘要

尽管细胞外囊泡(EVs)具有包裹细胞内化合物并将其转移到附近或远处受体细胞的天然能力,但有意将货物分子装载到EVs仍然是一项具有挑战性的工作。地层前的EV加载(即在EV生物发生期间)相比于地层后的EV加载(即在EV分离后)具有优势,因为EV的完整性和组成受到的干扰最小。预成型电动汽车装载主要是通过生产细胞的基因工程来实现的,这是非常耗时的,而且对于可以纳入电动汽车的分子类型来说不是很灵活。在这项工作中,我们研究了通过将货物直接运送到生产细胞的细胞质中来将货物分子装载到电动汽车中的可能性,这些细胞质随后可以在电动汽车形成时被封装到电动汽车中。对于货物分子的细胞质递送,我们评估了光穿孔的使用。这种膜破坏技术已经被证明可以成功地将大范围的货物分子输送到几乎任何类型的细胞中,同时对细胞的正常功能和体内平衡的影响最小。作为概念验证,我们将荧光标记的葡聚糖大分子和抗egfp纳米体注入经gag-EGFP融合蛋白基因工程改造的HEK293T细胞,并将其穿梭到电动汽车中。在分泌的电动汽车中,货物和EGFP荧光的共定位可以作为电动汽车成功装载的方便读数。我们发现光穿孔对EV膜表面分子的浓度、大小、zeta电位以及EV膜表面分子的富集等特性影响很小。我们发现,使用EGFP靶向纳米体可产生高达53%的ev负载(相对于EGFP ev的数量),而非靶向葡聚糖分子平均产生12%的ev负载(相对于EGFP ev的数量)。这些结果突出了光穿孔在电动汽车预成型加载中的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pre-formation loading of extracellular vesicles with exogenous molecules using photoporation.

Despite the natural capacity of extracellular vesicles (EVs) to encapsulate intracellular compounds and transfer these to nearby or distant recipient cells, the intentional loading of EVs with cargo molecules remains a challenging endeavor. Pre-formation EV loading (i.e., during EV biogenesis), offers advantages compared to post-formation loading (i.e., after EV isolation), as EV integrity and composition are minimally perturbed. Pre-formation EV loading is primarily achieved through the genetic engineering of the producer cell, which is time consuming and not very flexible regarding the types of molecules that can be incorporated into EVs. In this work, we investigated the possibility of loading cargo molecules into EVs by delivering the cargo directly into the cytosol of the producer cells, which can subsequently be encapsulated into EVs as they are formed. For the cytosolic delivery of cargo molecules, we evaluated the use of photoporation. This membrane disruption technology has been demonstrated to successfully deliver a broad range of cargo molecules into virtually any cell type, while minimally impacting the cell's normal functioning and homeostasis. As a proof-of-concept, we delivered fluorescently labeled dextran macromolecules and anti-EGFP nanobodies into HEK293T cells genetically engineered with gag-EGFP fusion proteins, which are shuttled into EVs. Colocalization of cargo and EGFP fluorescence in secreted EVs can then serve as a convenient readout for successful EV loading. We established that photoporation had minimal impact on EV characteristics such as concentration, size, zeta potential and the enrichment of EV tetraspanin membrane surface molecules. We found that using EGFP-targeted nanobodies resulted in up to 53% loaded EVs (relative to the amount of EGFP EVs), while non-targeted dextran molecules produced on average 12% loaded EVs (relative to the amount of EGFP EVs). These results highlight the promise of photoporation for pre-formation loading of EVs.

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来源期刊
Journal of Nanobiotechnology
Journal of Nanobiotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
13.90
自引率
4.90%
发文量
493
审稿时长
16 weeks
期刊介绍: Journal of Nanobiotechnology is an open access peer-reviewed journal communicating scientific and technological advances in the fields of medicine and biology, with an emphasis in their interface with nanoscale sciences. The journal provides biomedical scientists and the international biotechnology business community with the latest developments in the growing field of Nanobiotechnology.
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