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在生物标志物研究中使用神经元细胞外囊泡的前景和挑战。

Prospects and challenges in using neuronal extracellular vesicles in biomarker research.

机构信息

D'Or Institute for Research and Education, Rio de Janeiro, Brazil.

Institute of Medical Biochemistry Leopoldo de Meis, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Alzheimers Dement. 2024 Sep;20(9):6632-6638. doi: 10.1002/alz.13918. Epub 2024 Jul 15.

DOI:10.1002/alz.13918
PMID:39009473
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11497720/
Abstract

Extracellular vesicles (EVs) hold promise as a source of disease biomarkers. The diverse molecular cargo of EVs can potentially indicate the status of their tissue of origin, even against the complex background of whole plasma. The main tools currently available for assessing biomarkers of brain health include brain imaging and analysis of the cerebrospinal fluid of patients. Given the costs and difficulties associated with these methods, isolation of EVs of neuronal origin (NEVs) from the blood is an attractive approach to identify brain-specific biomarkers. This perspective describes current key challenges in EV- and NEV-based biomarker research. These include the relative low abundance of EVs, the lack of validated isolation methods, and the difficult search for an adequate target for immunocapturing NEVs. We discuss that these challenges must be addressed before NEVs can fulfill their potential for biomarker research. HIGHLIGHTS: NEVs are promising sources of biomarkers for brain disorders. Immunocapturing NEVs from complex biofluids presents several challenges. The choice of surface target for capture will determine NEV yield. Contamination by non-EV sources is relevant for biomarkers at low concentrations.

摘要

细胞外囊泡 (EVs) 有望成为疾病生物标志物的来源。EVs 的多种分子货物有可能表明其组织来源的状态,即使在整个血浆的复杂背景下也是如此。目前评估脑健康生物标志物的主要工具包括脑成像和对患者脑脊液的分析。鉴于这些方法的成本和困难,从血液中分离神经元来源的 EVs (NEVs) 是一种有吸引力的方法,可以识别脑特异性生物标志物。本文描述了基于 EV 和 NEV 的生物标志物研究中的当前关键挑战。这些挑战包括 EV 相对低丰度、缺乏经过验证的分离方法以及难以寻找合适的免疫捕获 NEV 靶标。我们讨论了在 NEV 能够充分发挥其在生物标志物研究中的潜力之前,必须解决这些挑战。要点:NEVs 是脑疾病生物标志物的有前途的来源。从复杂的生物流体中免疫捕获 NEVs 提出了几个挑战。捕获的表面靶标选择将决定 NEV 的产量。低浓度时,非 EV 来源的污染与生物标志物相关。

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