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二维和三维细胞培养中的动态转录因子活性分析。

Dynamic transcription factor activity profiling in 2D and 3D cell cultures.

机构信息

Department of Chemical and Biological Engineering, Northwestern University, 2145 Sheridan Rd./E156, Evanston, Illinois 60208-3120, USA.

出版信息

Biotechnol Bioeng. 2013 Feb;110(2):563-72. doi: 10.1002/bit.24718. Epub 2012 Sep 18.

Abstract

Live-cell assays to measure cellular function performed within 3D cultures have the potential to elucidate the underlying processes behind disease progression and tissue formation. Cells cultured in 3D interact and remodel their microenvironment and can develop into complex structures. We have developed a transcription factor (TF) activity array that uses bioluminescence imaging (BLI) of lentiviral delivered luminescent reporter constructs that allows for the non-invasive imaging of TF activity in both 2D and 3D culture. Imaging can be applied repeatedly throughout culture to capture dynamic TF activity, though appropriate normalization is necessary. We investigated in-well normalization using Gaussia or Renilla luciferase, and external well normalization using firefly luciferase. Gaussia and Renilla luciferase were each unable to provide consistent normalization for long-term measurement of TF activity. However, external well normalization provided low variability and accounted for changes in cellular dynamics. Using external normalization, dynamic TF activities were quantified for five TFs. The array captured expected changes in TF activity to stimuli, however the array also provided dynamic profiles within 2D and 3D that have not been previously characterized. The development of the technology to dynamically track TF activity within cells cultured in both 2D and 3D can provide greater understanding of complex cellular processes.

摘要

活细胞分析测量三维培养物中的细胞功能,具有阐明疾病进展和组织形成背后潜在过程的潜力。在 3D 中培养的细胞相互作用并重塑其微环境,并且可以发展成复杂的结构。我们开发了一种转录因子 (TF) 活性阵列,该阵列使用慢病毒传递的发光报告基因构建体的生物发光成像 (BLI),允许在 2D 和 3D 培养物中对 TF 活性进行非侵入性成像。可以在整个培养过程中重复进行成像,以捕获动态 TF 活性,尽管需要适当的归一化。我们使用海肾萤光素酶或 Renilla 萤光素酶进行孔内归一化,并使用萤火虫萤光素酶进行外部孔归一化进行了研究。海肾萤光素酶和 Renilla 萤光素酶都不能为 TF 活性的长期测量提供一致的归一化。然而,外部孔归一化提供了低变异性并解释了细胞动力学的变化。使用外部归一化,对五种 TF 进行了动态 TF 活性的定量分析。该阵列捕捉到了 TF 活性对刺激的预期变化,但该阵列还提供了以前未表征的 2D 和 3D 内的动态分布。该技术的发展能够动态跟踪在 2D 和 3D 培养的细胞中的 TF 活性,可以更好地理解复杂的细胞过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f59/4073638/24422d603247/nihms-579864-f0001.jpg

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