Yatouji Sonia, Trussardi-Regnier Aurelie, Trentesaux Chantal, Liautaud-Roger Françoise, Dufer Jean
Unité MéDIAN-CNRS UMR 6142, IFR 53, Faculté de Pharmacie, 51096 Reims cedex, France.
Int J Oncol. 2003 Oct;23(4):1225-30.
Previous studies have demonstrated that multidrug-resistant leukemic cells displayed nuclear texture changes. In this work, the human ovarian carcinoma cell line IGROV1 and its multidrug-resistant variant OV1/VCR were studied. Cell smears of these cell populations were analysed by image cytometry. As compared to sensitive cells, OV1/VCR display a chromatin global decondensation as assessed by textural features analysis. In order to correlate this decondensation with alterations in chromatin structure, DNase I was used. OV1/VCR DNA displayed an increased DNase I sensitivity, suggesting an increased chromatin accessibility. Furthermore, OV1/VCR cells displayed an increased level in acetylated histone H4, a mechanism known to be associated with transcriptionally active chromatin and relaxed chromatin conformation.
先前的研究表明,多药耐药白血病细胞呈现出核纹理变化。在这项研究中,对人卵巢癌细胞系IGROV1及其多药耐药变体OV1/VCR进行了研究。通过图像细胞术分析了这些细胞群体的细胞涂片。与敏感细胞相比,通过纹理特征分析评估,OV1/VCR显示出染色质整体解聚。为了将这种解聚与染色质结构的改变相关联,使用了DNase I。OV1/VCR DNA对DNase I的敏感性增加,表明染色质可及性增加。此外,OV1/VCR细胞中乙酰化组蛋白H4水平升高,这是一种已知与转录活性染色质和松弛染色质构象相关的机制。