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三维培养通过调节Raf-1表达来调控纤连蛋白基质组装。

Three-dimensional culture regulates Raf-1 expression to modulate fibronectin matrix assembly.

作者信息

Winters B S, Raj B K Mohan, Robinson E E, Foty R A, Corbett S A

机构信息

Department of Surgery, Robert Wood Johnson Medical School, New Brunswick, NJ 08903, USA.

出版信息

Mol Biol Cell. 2006 Aug;17(8):3386-96. doi: 10.1091/mbc.e05-09-0849. Epub 2006 May 17.

Abstract

Oncogenic transformation has been associated with decreased fibronectin (FN) matrix assembly. For example, both the HT-1080 fibrosarcoma and MAT-LyLu cell lines fail to assemble a FN matrix when grown in monolayer culture (2-dimensional [2D] system). In this study, we show that these cells regain the ability to assemble a FN matrix when they are grown as aggregates (3-dimensional [3D] system). FN matrix assembly in 3D correlates with decreased Raf-1 protein expression compared with cells grown in monolayer culture. This effect is associated with reduced Raf-1 mRNA levels as determined by quantitative RT-PCR and not proteasome-mediated degradation of endogenous Raf-1. Interestingly, transient expression of a Raf-1 promoter-reporter construct demonstrates increased Raf-1 promoter activity in 3D, suggesting that the transition to 3D culture may modulate Raf-1 mRNA stability. Finally, to confirm that decreased Raf-1 expression results in increased FN matrix assembly, we used both pharmacological and small interfering RNA knockdown of Raf-1. This restored the ability of cells in 2D culture to assemble a FN matrix. Moreover, overexpression of Raf-1 prevented FN matrix assembly by cells cultured in 3D, resulting in decreased aggregate compaction. This work provides new insight into how the cell microenvironment may influence Raf-1 expression to modulate cell-FN interactions in 3D.

摘要

致癌转化与纤连蛋白(FN)基质组装减少有关。例如,HT-1080纤维肉瘤细胞系和MAT-LyLu细胞系在单层培养(二维[2D]系统)中生长时均无法组装FN基质。在本研究中,我们发现这些细胞在聚集体状态下生长(三维[3D]系统)时恢复了组装FN基质的能力。与单层培养的细胞相比,3D条件下的FN基质组装与Raf-1蛋白表达降低相关。通过定量逆转录聚合酶链反应确定,这种效应与Raf-1 mRNA水平降低有关,而非蛋白酶体介导的内源性Raf-1降解。有趣的是,Raf-1启动子-报告基因构建体的瞬时表达表明,在3D条件下Raf-1启动子活性增加,这表明向3D培养的转变可能调节Raf-1 mRNA的稳定性。最后,为了证实Raf-1表达降低导致FN基质组装增加,我们使用了Raf-1的药理学抑制剂和小干扰RNA敲低技术。这恢复了2D培养细胞组装FN基质的能力。此外,Raf-1的过表达阻止了3D培养细胞的FN基质组装,导致聚集体紧实度降低。这项工作为细胞微环境如何影响Raf-1表达以调节3D条件下细胞与FN的相互作用提供了新的见解。

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