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利用空间光调制的抗衍射光片(ADLS)流式细胞术

Flow Cytometry with Anti-Diffraction Light Sheet (ADLS) by Spatial Light Modulation.

作者信息

Gong Yanyan, Zeng Ming, Zhu Yueqiang, Li Shangyu, Zhao Wei, Zhang Ce, Zhao Tianyun, Wang Kaige, Yang Jiangcun, Bai Jintao

机构信息

State Key Laboratory of Photon-Technology in Western China Energy, International Collaborative Center on Photoelectric Technology and Nano Functional Materials, Institute of Photonics & Photon Technology, Northwest University, Xi'an 710127, China.

School of Automation, Northwestern Polytechnical University, Xi'an 710072, China.

出版信息

Micromachines (Basel). 2023 Mar 19;14(3):679. doi: 10.3390/mi14030679.

DOI:10.3390/mi14030679
PMID:36985086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10054044/
Abstract

Flow cytometry is a widespread and powerful technique whose resolution is determined by its capacity to accurately distinguish fluorescently positive populations from negative ones. However, most informative results are discarded while performing the measurements of conventional flow cytometry, e.g., the cell size, shape, morphology, and distribution or location of labeled exosomes within the unpurified biological samples. Herein, we propose a novel approach using an anti-diffraction light sheet with anisotroic feature to excite fluorescent tags. Constituted by an anti-diffraction Bessel-Gaussian beam array, the light sheet is 12 μm wide, 12 μm high, and has a thickness of ~0.8 μm. The intensity profile of the excited fluorescent signal can, therefore, reflect the size and allow samples in the range from O (100 nm) to 10 μm (e.g., blood cells) to be transported via hydrodynamic focusing in a microfluidic chip. The sampling rate is 500 kHz, which provides a capability of high throughput without sacrificing the spatial resolution. Consequently, the proposed anti-diffraction light sheet flow cytometry (ADLSFC) can obtain more informative results than the conventional methodologies, and is able to provide multiple characteristics (e.g., the size and distribution of fluorescent signal) helping to distinguish the target samples from the complex backgrounds.

摘要

流式细胞术是一种广泛应用且功能强大的技术,其分辨率取决于准确区分荧光阳性群体和阴性群体的能力。然而,在进行传统流式细胞术测量时,大多数有用的结果都被舍弃了,例如未纯化生物样品中细胞的大小、形状、形态以及标记外泌体的分布或位置。在此,我们提出一种使用具有各向异性特征的抗衍射光片来激发荧光标记的新方法。该光片由抗衍射贝塞尔 - 高斯光束阵列构成,宽12μm,高12μm,厚度约为0.8μm。因此,激发荧光信号的强度分布可以反映样品大小,并允许从O(100nm)到10μm范围内的样品(如血细胞)通过微流控芯片中的流体动力聚焦进行输送。采样率为500kHz,在不牺牲空间分辨率的情况下提供了高通量能力。因此,所提出的抗衍射光片流式细胞术(ADLSFC)能够比传统方法获得更多有用的结果,并且能够提供多种特征(如荧光信号的大小和分布),有助于从复杂背景中区分目标样品。

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本文引用的文献

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开发一种水折射率匹配的微针,并将其集成到光片显微镜系统中,用于连续胚胎细胞成像。
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Single-cell analysis by mass cytometry reveals metabolic states of early-activated CD8 T cells during the primary immune response.通过质谱细胞术对单细胞进行分析,揭示了初级免疫反应期间早期激活的 CD8 T 细胞的代谢状态。
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