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

被引:17
作者
Bellis, Abigail D. [1 ,2 ]
Bernabe, Beatriz Penalver [1 ]
Weiss, Michael S. [1 ]
Shin, Seungjin [1 ]
Weng, Stanley [1 ]
Broadbelt, Linda J. [1 ]
Shea, Lonnie D. [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Inst Bionanotechnol Med IBNAM, Chicago, IL 60611 USA
[3] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
cellular array; transcription factor activity; bioluminescence imaging; 3D culture; GENE-EXPRESSION; MCF-7; PROTEIN; MATURATION;
D O I
10.1002/bit.24718
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. Biotechnol. Bioeng. 2013; 110: 563572. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:563 / 572
页数:10
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