血液中组织特异性细胞外囊泡的检测与分离

Lauren Newman, Andrew Rowland
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引用次数: 0

摘要

细胞外囊泡(EVs)是由几乎所有细胞类型释放的纳米级膜结合颗粒,作为组织内和通过血液跨器官的信使。电动汽车封装了多种分子货物,反映了其起源细胞的表型状态,使其成为液体活检应用的有希望的候选者。然而,循环EV的异质性,包括来自各种细胞类型和非囊泡实体(如脂蛋白)的颗粒,为分离组织特异性EV群体带来了重大挑战。本文综述了目前从血液中检测和分离组织特异性ev的方法,重点是利用表面标记物表达特异性的免疫亲和力捕获(IAC)策略。主要考虑因素,包括标记的选择和验证,以及EV亚型分型和分离协议的进展进行了讨论。强调了诸如标记物交叉反应性、EV生物发生和运输动力学等挑战,以强调实现临床应用的复杂性。通过对组织特异性标记物和分离技术的综述,本文旨在促进基于ev的生物标记物的开发,提高其特异性和敏感性,从而实现器官功能和疾病的微创监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Detection and Isolation of Tissue-Specific Extracellular Vesicles From the Blood

Detection and Isolation of Tissue-Specific Extracellular Vesicles From the Blood

Extracellular vesicles (EVs) are nanosized, membrane-bound particles released by virtually all cell types, serving as messengers within tissues and across organs via the bloodstream. EVs encapsulate diverse molecular cargo that reflects the phenotypic state of their originating cells, making them promising candidates for liquid biopsy applications. However, the heterogeneity of circulating EVs, comprising particles from various cell types and non-vesicular entities like lipoproteins, poses significant challenges for isolating tissue-specific EV populations. This review examines current methodologies for detecting and isolating tissue-specific EVs from blood, focusing on immunoaffinity capture (IAC) strategies that leverage surface marker expression for specificity. Key considerations, including the selection and validation of markers, are discussed alongside advances in EV subtyping and isolation protocols. Challenges such as marker cross-reactivity, EV biogenesis and transport dynamics are highlighted to underscore the complexity of achieving clinical utility. By providing an overview of validated tissue-specific markers and isolation techniques, this review aims to facilitate the development of EV-based biomarkers with enhanced specificity and sensitivity, enabling minimally invasive monitoring of organ function and disease.

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