Dzierzewicz Zofia, Orchel Arkadiusz, Weglarz Ludmila, Latocha Małgorzata, Wilczok Tadeusz
Department of Molecular Biology, Biochemistry and Biopharmacy, Silesian Medical University of Silesia, Sosnowiec, Poland.
Acta Biochim Pol. 2002;49(1):211-20.
Gut-derived adenocarcinoma Caco-2 cells were treated with sodium butyrate (NaB) at physiologically relevant concentrations. We characterized its effects on proliferation, differentiation, apoptosis, adhesion to the solid support and interleukin-8 secretion. Differentiation was determined by brush border alkaline phosphatase activity. Apoptosis was assessed by acridine orange and Hoechst stains. Differentiation and apoptosis were analyzed in both adherent and floating cell populations. The transformed Caco-2 cells did not retain their malignant phenotype in the presence of NaB. They appeared to undergo a change in the phenotype induced by NaB, as indicated by reduced proliferation, enhanced differentiation, stimulation of apoptosis leading to decreased viability of cells, and stimulation of interleukin-8 secretion. Considering all the above facts and data, we postulate that Caco-2 cells cultured in NaB supplemented medium could regain the phenotypic characteristics of the phenotype of the parent cell from which originated the Caco-2 line.
用生理相关浓度的丁酸钠(NaB)处理源自肠道的腺癌Caco-2细胞。我们表征了其对增殖、分化、凋亡、对固体支持物的粘附以及白细胞介素-8分泌的影响。通过刷状缘碱性磷酸酶活性来确定分化。通过吖啶橙和 Hoechst 染色评估凋亡。在贴壁细胞群和悬浮细胞群中分析分化和凋亡。在存在 NaB 的情况下,转化的 Caco-2 细胞并未保留其恶性表型。它们似乎经历了由 NaB 诱导的表型变化,表现为增殖减少、分化增强、凋亡受刺激导致细胞活力降低以及白细胞介素-8 分泌受刺激。考虑到上述所有事实和数据,我们推测在补充了 NaB 的培养基中培养的 Caco-2 细胞可以恢复产生 Caco-2 细胞系的亲代细胞表型的表型特征。