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Quantification of the Effect of Toxicants on the Intracellular Kinetic Energy and Cross-Sectional Area of Mammary Epithelial Organoids by OCT Fluctuation Spectroscopy

机译:通过OCT波动光谱定量分析有毒物质对乳腺上皮有机体的细胞内动能和横截面积的影响

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摘要

The ability to assess toxicant exposures of 3D in vitro mammary models that recapitulate the tissue microenvironment can aid in our understanding of environmental exposure risk over time. Longitudinal studies of 3D model systems, however, are cumbersome and suffer from a lack of high-throughput toxicological assays. In this study, we establish a noninvasive and label-free optical coherence tomography (OCT)-based imaging platform for tracking exposure-response relationships in 3D human mammary epithelial organoid models. The OCT-based assay includes metrics that quantify organoid intracellular kinetic energy and cross-sectional area (CSA). We compare the results to those obtained using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) mitochondrial dye conversion assay. Both estrogen receptor (ER)-positive (MCF7) and ER-negative (MCF10DCIS.com) breast cell lines were studied, beginning one hour after exposure and continuing for several days. Six days of exposure to 17β-estradiol or the selective ER modulator 4-hydroxytamoxifen respectively increased or decreased MCF7 organoid CSA (p < .01), consistent with the role of estrogen signaling in ER-positive mammary epithelial cell proliferation. We also observed a significant decrease in the intracellular kinetic energy of MCF10DCIS.com organoids after 24 h of exposure to doxorubicin, a cytotoxic intercalating agent that causes DNA double-strand breaks (p < .01). MTT-based metabolic activity of MCF10DCIS.com organoids after 48 h of doxorubicin exposure decreased with dose in a similar manner as OCT-based energy metrics. These results demonstrate the feasibility of an OCT-based assay to quantify mammary epithelial cell toxicant response in vitro, noninvasively, longitudinally, and in the context of tissue microenvironments, providing a new high-throughput screening tool for toxicological studies.
机译:评估可概述组织微环境的3D体外乳腺模型的有毒物质暴露的能力可以帮助我们了解随着时间的推移环境暴露的风险。但是,对3D模型系统的纵向研究很麻烦,并且缺乏高通量毒理学检测方法。在这项研究中,我们建立了一个无创且无标签的光学相干断层扫描(OCT)为基础的成像平台,用于跟踪3D人乳腺上皮类器官模型中的暴露-反应关系。基于OCT的分析包括量化类器官细胞内动能和横截面积(CSA)的指标。我们将结果与使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H-溴化四唑(MTT)线粒体染料转化分析获得的结果进行比较。雌激素受体(ER)阳性(MCF7)和ER阴性(MCF10DCIS.com)乳腺癌细胞系均经过研究,从暴露后一小时开始,持续数天。暴露于17β-雌二醇或选择性ER调节剂4-羟基他莫昔芬的六天分别增加或减少MCF7类器官CSA(p <.01),与雌激素信号传导在ER阳性乳腺上皮细胞增殖中的作用一致。我们还观察到暴露于阿霉素(一种会引起DNA双链断裂的细胞毒性嵌入剂)24小时后,MCF10DCIS.com类器官的细胞内动能显着降低。阿霉素暴露48 h后,MCF10DCIS.com类器官的基于MTT的代谢活性随剂量的增加而降低,其方式与基于OCT的能量指标类似。这些结果证明了基于OCT的测定在体外,无创,纵向以及组织微环境的背景下定量乳腺上皮细胞毒性反应的可行性,为毒理学研究提供了一种新的高通量筛选工具。

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