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用红外量子点对单细胞中的生长因子进行计数,以测量离散刺激分布。

Counting growth factors in single cells with infrared quantum dots to measure discrete stimulation distributions.

机构信息

Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.

Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.

出版信息

Nat Commun. 2019 Feb 22;10(1):909. doi: 10.1038/s41467-019-08754-5.

Abstract

The distribution of single-cell properties across a population of cells can be measured using diverse tools, but no technology directly quantifies the biochemical stimulation events regulating these properties. Here we report digital counting of growth factors in single cells using fluorescent quantum dots and calibrated three-dimensional deconvolution microscopy (QDC-3DM) to reveal physiologically relevant cell stimulation distributions. We calibrate the fluorescence intensities of individual compact quantum dots labeled with epidermal growth factor (EGF) and demonstrate the necessity of near-infrared emission to overcome intrinsic cellular autofluoresence at the single-molecule level. When applied to human triple-negative breast cancer cells, we observe proportionality between stimulation and both receptor internalization and inhibitor response, reflecting stimulation heterogeneity contributions to intrinsic variability. We anticipate that QDC-3DM can be applied to analyze any peptidic ligand to reveal single-cell correlations between external stimulation and phenotypic variability, cell fate, and drug response.

摘要

使用各种工具可以测量细胞群体中单细胞特性的分布,但没有技术可以直接量化调节这些特性的生化刺激事件。在这里,我们报告了使用荧光量子点和校准的三维反卷积显微镜(QDC-3DM)对生长因子在单细胞中的数字计数,以揭示生理相关的细胞刺激分布。我们校准了用表皮生长因子(EGF)标记的单个紧凑量子点的荧光强度,并证明了近红外发射的必要性,以克服在单分子水平上的固有细胞内荧光。当应用于人类三阴性乳腺癌细胞时,我们观察到刺激与受体内化和抑制剂反应之间的比例关系,反映了刺激异质性对固有变异性的贡献。我们预计 QDC-3DM 可用于分析任何肽配体,以揭示外部刺激与表型变异性、细胞命运和药物反应之间的单细胞相关性。

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