Vallee Sebastien, Laforest Sullivan, Fouchier Francis, Montero Marie Pierre, Penel Claude, Champion Serge
Laboratoire de Biochimie Cellulaire, Faculté de Pharmacie, UMR 6032 CNRS, FR-13385 Marseille Cedex, France.
Exp Cell Res. 2004 Jul 1;297(1):165-85. doi: 10.1016/j.yexcr.2004.03.007.
As described for a long time, carcinoma-derived Caco-2 cells form a polarized epithelium in culture, whereas HT29-D4 cells are nonpolarized and undifferentiated but can form a polarized monolayer when cultured in a galactose-supplemented medium. Using NF-kappaB translocation and IL-8 and ICAM-1 gene activation as an index, we have studied the relationship between the differentiation state and the cell response to cytokines. We found that differentiated Caco-2 and HT29-D4 cells were responsive to both cytokines TNFalpha- and IL-1beta-mediated activation of NF-kappaB but that undifferentiated HT29-D4 cells were unresponsive to IL-1beta. However, the expression of endogenous ICAM-1 and IL-8 genes was upregulated by these cytokines in either cell lines differentiated or not. Upregulation of ICAM-1 gene occurred when IL-1beta or TNFalpha was added to the basal, but not apical surface of the differentiated epithelia. Finally, it appeared that in polarized HT29-D4 cells, the IL-1beta-induced translocation of NF-kappaB was connected to PKCdelta translocation.
长期以来的研究表明,源自癌细胞的Caco-2细胞在培养中形成极化上皮,而HT29-D4细胞是非极化且未分化的,但在补充半乳糖的培养基中培养时可形成极化单层。以NF-κB易位以及IL-8和ICAM-1基因激活为指标,我们研究了分化状态与细胞对细胞因子反应之间的关系。我们发现,分化的Caco-2和HT29-D4细胞对细胞因子TNFα和IL-1β介导的NF-κB激活均有反应,但未分化的HT29-D4细胞对IL-1β无反应。然而,这些细胞因子在已分化或未分化的细胞系中均上调了内源性ICAM-1和IL-8基因的表达。当将IL-1β或TNFα添加到分化上皮的基底表面而非顶端表面时,ICAM-1基因发生上调。最后看来,在极化的HT29-D4细胞中,IL-1β诱导的NF-κB易位与PKCδ易位有关。