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基于微流控的低侵入性细胞分选技术的多组学特征分析。

Multiomics Characterization of a Less Invasive Microfluidic-Based Cell Sorting Technique.

机构信息

Dynamic Omics, Centre for Genomics Research (CGR), Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, Maryland 20878, United States.

Oncology Cell Therapy, ICC, Oncology R&D, AstraZeneca, Gaithersburg, Maryland 20878, United States.

出版信息

J Proteome Res. 2024 Aug 2;23(8):3096-3107. doi: 10.1021/acs.jproteome.3c00773. Epub 2024 Feb 28.

Abstract

Fluorescence-activated cell sorting (FACS) is a specialized technique to isolate specific cell subpopulations with a high level of recovery and accuracy. However, the cell sorting procedure can impact the viability and metabolic state of cells. Here, we performed a comparative study and evaluated the impact of traditional high-pressure charged droplet-based and microfluidic chip-based sorting on the metabolic and phosphoproteomic profile of different cell types. While microfluidic chip-based sorted cells more closely resembled the unsorted control group for most cell types tested, the droplet-based sorted cells showed significant metabolic and phosphoproteomic alterations. In particular, greater changes in redox and energy status were present in cells sorted with the droplet-based cell sorter along with larger shifts in proteostasis. C-isotope tracing analysis on cells recovering postsorting revealed that the sorter-induced suppression of mitochondrial TCA cycle activity recovered faster in the microfluidic chip-based sorted group. Apart from this, amino acid and lipid biosynthesis pathways were suppressed in sorted cells, with minimum impact and faster recovery in the microfluidic chip-based sorted group. These results indicate microfluidic chip-based sorting has a minimum impact on metabolism and is less disruptive compared to droplet-based sorting.

摘要

荧光激活细胞分选(FACS)是一种专门的技术,可以高度回收和准确地分离特定的细胞亚群。然而,细胞分选过程会影响细胞的活力和代谢状态。在这里,我们进行了一项比较研究,评估了传统的高压充电液滴式和微流控芯片式分选对不同细胞类型代谢和磷酸化蛋白质组学特征的影响。虽然基于微流控芯片分选的细胞在大多数测试的细胞类型中更接近未分选的对照组,但基于液滴的分选细胞显示出明显的代谢和磷酸化蛋白质组学改变。特别是,基于液滴的细胞分选器分选的细胞中氧化还原和能量状态的变化更大,同时蛋白质稳态的变化更大。对分选后恢复的细胞进行 C-同位素示踪分析表明,基于微流控芯片分选的细胞中,分选诱导的线粒体 TCA 循环活性抑制恢复得更快。除此之外,氨基酸和脂质生物合成途径在分选细胞中受到抑制,基于微流控芯片分选的细胞中受到的影响最小,恢复速度也更快。这些结果表明,与基于液滴的分选相比,基于微流控芯片的分选对代谢的影响最小,干扰也更小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35a4/11301668/662a3cd6697b/pr3c00773_0001.jpg

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