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Influence of species and processing parameters on recovery and content of brain tissue-derived extracellular vesicles

机译:物种及加工参数对脑组织衍生细胞外囊泡恢复和含量的影响

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摘要

Extracellular vesicles (EVs) are involved in a wide range of physiological and pathological processes by shuttling material out of and between cells. Tissue EVs may thus lend insights into disease mechanisms and also betray disease when released into easily accessed biological fluids. Since brain-derived EVs (bdEVs) and their cargo may serve as biomarkers of neurodegenerative diseases, we evaluated modifications to a published, rigorous protocol for separation of EVs from brain tissue and studied effects of processing variables on quantitative and qualitative outcomes. To this end, size exclusion chromatography (SEC) and sucrose density gradient ultracentrifugation were compared as final separation steps in protocols involving stepped ultracentrifugation. bdEVs were separated from brain tissues of human, macaque, and mouse. Effects of tissue perfusion and a model of post-mortem interval (PMI) before final bdEV separation were probed. MISEV2018-compliant EV characterization was performed, and both small RNA and protein profiling were done. We conclude that the modified, SEC-employing protocol achieves EV separation efficiency roughly similar to a protocol using gradient density ultracentrifugation, while decreasing operator time and, potentially, variability. The protocol appears to yield bdEVs of higher purity for human tissues compared with those of macaque and, especially, mouse, suggesting opportunities for optimization. Where possible, perfusion should be performed in animal models. The interval between death/tissue storage/processing and final bdEV separation can also affect bdEV populations and composition and should thus be recorded for rigorous reporting. Finally, different populations of EVs obtained through the modified method reported herein display characteristic RNA and protein content that hint at biomarker potential. To conclude, this study finds that the automatable and increasingly employed technique of SEC can be applied to tissue EV separation, and also reveals more about the importance of species-specific and technical considerations when working with tissue EVs. These results are expected to enhance the use of bdEVs in revealing and understanding brain disease.
机译:细胞外囊泡(EVS)通过穿梭于细胞之间的材料和细胞之间的含量涉及各种生理和病理过程。因此,组织EV可能会在释放到易于进入的生物流体时,涉及疾病机制和背叛疾病。由于脑衍生的EVS(BDEVS)及其货物可以作为神经变性疾病的生物标志物,我们评估了对来自脑组织中EV的公布的,严谨的方案的改性,并研究了处理变量对定量和定性结果的影响。为此,将尺寸排阻色谱(SEC)和蔗糖密度梯度超速离心与涉及步进超速离心的方案中的最终分离步骤进行比较。 BDEVs与人,猕猴和小鼠的脑组织分开。探针在最终BDEV分离之前的组织灌注和验尸间隔(PMI)模型的影响。进行MISEV2018标准的EV表征,并进行小RNA和蛋白质分析。我们得出结论,改进的秒的采用协议通过使用梯度密度超速离心的协议实现了EV分离效率,同时降低了操作员时间,并且可能是可变性。与猕猴的那些,该方案似乎与人类组织的纯度更高纯度的BDEV,并且尤其是小鼠,表明优化的机会。在可能的情况下,灌注应在动物模型中进行。死亡/组织存储/处理和最终BDEV分离之间的间隔也可以影响BDEV群体和组成,因此应记录为严格的报告。最后,通过本文报道的通过修饰的方法获得的不同群体显示在生物标志物电位下暗示的特征RNA和蛋白质含量。为了得出结论,本研究发现,当使用组织EVS时,可以应用于组织EV分离的自动和越来越采用的SEC技术。这些结果预计将增强BDEVS在揭示和理解脑疾病方面的使用。

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