Corbière C, Battu S, Liagre B, Cardot P J P, Beneytout J L
Laboratoire de Biochimie, Faculté de Pharmacie, EA 1085 Biomolécules et Cibles Cellulaires Tumorales, Université de Limoges, 2 Rue du Dr. Marcland, 87025 Limoges Cedex, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Sep 5;808(2):255-62. doi: 10.1016/j.jchromb.2004.05.026.
Apoptosis is one of the most important phenomena of cellular biology. Sedimentation field flow fractionation (SdFFF) has been described as an effective tool for cell separation, respecting integrity and viability. Because SdFFF takes advantage of intrinsic properties of eluted cells (size, density, shape or rigidity), we investigated the capacity of SdFFF in monitoring the early and specific biophysical modifications which occurred during cellular apoptosis induction. Then, we used, as an in vitro cellular apoptosis model, the association between human 1547 osteosarcoma cells and diosgenin, a plant steroid known to induce apoptosis. Four other molecules were studied: hecogenin, tigogenin, staurosporine and MG132. Our results demonstrated a correlation between SdFFF elution profile changes (peak shape modification and retention ratio evolution) and effective apoptosis induction. For the first time, we demonstrated that SdFFF could be used to monitor apoptosis induction as early as 6 h incubation, suggesting different applications such as screening series of molecules to evaluate their ability to induce apoptosis, or sorting apoptotic cells to study apoptosis pathway.
细胞凋亡是细胞生物学中最重要的现象之一。沉降场流分离法(SdFFF)已被描述为一种用于细胞分离的有效工具,能保持细胞的完整性和活力。由于SdFFF利用了洗脱细胞的固有特性(大小、密度、形状或刚性),我们研究了SdFFF监测细胞凋亡诱导过程中早期和特定生物物理变化的能力。然后,我们将人1547骨肉瘤细胞与薯蓣皂苷元(一种已知可诱导细胞凋亡的植物甾体)的结合作为体外细胞凋亡模型。还研究了其他四种分子:海柯皂苷元、替告皂苷元、星形孢菌素和MG132。我们的结果表明,SdFFF洗脱曲线的变化(峰形改变和保留率变化)与有效的细胞凋亡诱导之间存在相关性。我们首次证明,SdFFF可用于在孵育6小时时就监测细胞凋亡诱导,这表明了其不同的应用,如筛选一系列分子以评估它们诱导细胞凋亡的能力,或分选凋亡细胞以研究细胞凋亡途径。