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对异柠檬酸脱氢酶1(IDH1)突变的胶质母细胞瘤细胞单个大型细胞外囊泡硬度的非接触式微流控分析

Non-contact microfluidic analysis of the stiffness of single large extracellular vesicles from IDH1-mutated glioblastoma cells.

作者信息

Jeong Mi Ho, Im Hyungsoon, Dahl Joanna B

机构信息

Center for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.

Department of Radiology, Massachusetts General Hospital, Boston, MA 02114, USA.

出版信息

Adv Mater Technol. 2023 Apr 6;8(7). doi: 10.1002/admt.202201412. Epub 2023 Jan 29.

Abstract

In preparation for leveraging extracellular vesicles (EVs) for disease diagnostics and therapeutics, fundamental research is being done to understand EV biological, chemical, and physical properties. Most published studies have investigated nanoscale EVs and focused on EV biochemical content. There is much less understanding of large microscale EV characteristics and EV mechanical properties. We recently introduced a non-contact microfluidic technique that measures the stiffness of large EVs (>1 μm diameter). This pilot study probes the robustness of the microfluidic technique to distinguish between EV populations by comparing stiffness distributions of large EVs derived from glioblastoma cell lines. EVs derived from cells expressing the IDH1 mutation, a common glioblastoma mutation known to disrupt lipid metabolism, were stiffer than those expressed from wild-type cells in a statistical comparison of sample medians. A supporting lipidomics analysis showed that the IDH1 mutation increased the amount of saturated lipids in EVs. Taken together, these data encourage further investigation into the potential of high-throughput microfluidics to distinguish between large EV populations that differ in biomolecular composition. These findings contribute to the understanding of EV biomechanics, in particular for the less studied microscale EVs.

摘要

为利用细胞外囊泡(EVs)进行疾病诊断和治疗做准备,正在开展基础研究以了解EVs的生物学、化学和物理特性。大多数已发表的研究都调查了纳米级的EVs,并聚焦于EVs的生化成分。对于较大的微米级EVs的特性和EVs的机械性能了解较少。我们最近引入了一种非接触式微流控技术,可测量大型EVs(直径>1μm)的硬度。这项初步研究通过比较源自胶质母细胞瘤细胞系的大型EVs的硬度分布,探究了微流控技术区分不同EV群体的稳健性。在样本中位数的统计比较中,源自表达IDH1突变(一种已知会破坏脂质代谢的常见胶质母细胞瘤突变)的细胞的EVs,比野生型细胞表达的EVs更硬。一项配套的脂质组学分析表明,IDH1突变增加了EVs中饱和脂质的含量。综上所述,这些数据鼓励进一步研究高通量微流控技术区分生物分子组成不同的大型EV群体的潜力。这些发现有助于理解EV生物力学,特别是对于研究较少的微米级EVs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45cb/10465107/a8b5ee430e32/nihms-1872393-f0002.jpg

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