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Imaging platforms to dissect the in vivo communication, biodistribution and controlled release of extracellular vesicles

期刊

JOURNAL OF CONTROLLED RELEASE
卷 360, 期 -, 页码 549-563

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ELSEVIER
DOI: 10.1016/j.jconrel.2023.06.039

关键词

Extracellular vesicles; Biodistribution; Imaging platforms; Controlled release of extracellular vesicles; In vivo communication

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Extracellular vesicles (EVs) act as communication vehicles for exchanging bioactive molecules between cells. Understanding their role in cellular communication is crucial for evaluating their biological, diagnostic, and therapeutic potential. Controlled release of EVs for regenerative medicine applications has been explored, and evaluating their release profile is important for correlating with biological activity. This article provides an overview of EV imaging platforms, discusses different EV labeling processes, and highlights the relevance of imaging platforms in studying the tropism, biological role, and release profile of EVs.
Extracellular vesicles (EVs) work as communication vehicles, allowing the exchange of bioactive molecules (microRNAs, mRNAs, proteins, etc) between neighbouring and distant cells in the organism. EVs are thus important players in several physiological and pathological processes. Thus, it is critical to understand their role in cellular/organ communication to fully evaluate their biological, diagnosis and therapeutic potential. In addition, recent studies have explored the controlled release of EVs for regenerative medicine applications and thus the evaluation of their release profile is important to correlate with biological activity. Here, we give a brief introduction about EV imaging platforms in terms of their sensitivity, penetration depth, cost, and operational simplicity, followed by a discussion of different EV labelling processes with their advantages and limitations. Next, we cover the relevance of these imaging platforms to dissect the tropism and biological role of endogenous EVs. We also cover the relevance of imaging platforms to monitor the accumulation of exogenous EVs and their potential cellular targets. Finally, we highlight the importance of imaging platforms to investigate the release profile of EVs from different controlled systems.

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