Hussain Mohammed Tayab, Austin-Williams Shani, McCay Joel, Hayat Hedayatullah, Wright Thomas D, Christoforou Marilena, Ykema Ella, Perretti Mauro, Cooper Dianne, Margraf Andreas
Centre for Biochemical Pharmacology, William Harvey Research Institute, Faculty of Medicine and Dentistry, Queen Mary University of London, London, UK.
Centre for Haemato-Oncology, Barts Cancer Institute, Faculty of Medicine and Dentistry, Queen Mary University of London, London, UK.
J Extracell Vesicles. 2025 Sep;14(9):e70127. doi: 10.1002/jev2.70127.
Extracellular vesicles (EVs) are small anuclear cellular membrane encapsulated fragments of importance for cellular interaction and transfer of information. These small vesicles, diverse in size and functionality, can be obtained from cells, tissues and bodily fluids. A complicated step for obtaining EVs from whole organs is understanding the optimal methodology for organ processing. In this study, we have examined two different techniques: one enzymatic and one novel non-enzymatic automated tissue dissociation (ATD) machine. Animals were perfused, organs extracted, and techniques comparatively applied. We have used these techniques for organ-based dissociation followed by EV isolation from the dissociated tissues (heart, kidney, lung). While both approaches allow isolation of intact EVs there are distinct differences in overall cell and particle yields. Our study highlights tissue specific inter-organ variability and differential impact of dissociation strategies on organ-based EV profiles, as well as cellular characteristics. Our findings indicate that EV yields and characteristics varies between enzymatic and ATD techniques as well as between organs with highest EV yield obtained from kidneys following enzymatic dissociation. Our findings can be rapidly transferred to other setups or developed to enable enumeration and characterization of EVs obtained from whole organs in physiological and pathological settings.
细胞外囊泡(EVs)是无细胞核的小细胞包膜包裹片段,对细胞间相互作用和信息传递至关重要。这些大小和功能各异的小囊泡可从细胞、组织和体液中获取。从整个器官获取细胞外囊泡的一个复杂步骤是了解器官处理的最佳方法。在本研究中,我们研究了两种不同技术:一种是酶解法,另一种是新型非酶自动组织解离(ATD)机器。对动物进行灌注、提取器官,并比较应用这些技术。我们使用这些技术进行基于器官的解离,随后从解离的组织(心脏、肾脏、肺)中分离细胞外囊泡。虽然两种方法都能分离出完整的细胞外囊泡,但在总体细胞和颗粒产量上存在明显差异。我们的研究突出了组织特异性的器官间变异性以及解离策略对基于器官的细胞外囊泡谱和细胞特征的不同影响。我们的研究结果表明,酶解法和自动组织解离技术之间以及不同器官之间,细胞外囊泡的产量和特征有所不同,酶解后从肾脏获得的细胞外囊泡产量最高。我们的研究结果可迅速应用于其他实验设置,或进一步发展以实现对生理和病理环境下从整个器官获得的细胞外囊泡进行计数和表征。