Pollack V, Scheiber K, Pfaller W, Schramek H
Department of Physiology, University of Innsbruck, Austria.
Biochem Biophys Res Commun. 1997 Dec 18;241(2):541-7. doi: 10.1006/bbrc.1997.7837.
MDCK-C7 cells dedifferentiated either by transient alkaline stress (C7F cells) or by transfection with a constitutively active mutant of the mitogen-activated protein kinase kinase MEK1 (C7caMEK1 cells) were analyzed by western blot and immunofluorescence microscopy to compare the expression of different cytokeratins, vimentin, and alpha-smooth muscle actin. Expression of all cytokeratins tested, the type II-neutral and basic cytokeratins CK5, CK7, CK8 as well as the type I-acidic keratins CK17 and CK19, was substantially reduced in dedifferentiated cell lines C7F and C7caMEK1 when compared with epithelial wild-type MDCK-C7 cells or mock-transfected MDCK-C7 cells. While vimentin expression was detected in all of the four MDCK-C7 cell lines examined, only the dedifferentiated cell lines C7F and C7caMEK1, which have been reported to express highly active ERK2, exhibited formation of alpha-smooth muscle actin-containing stress fibers. Taken together our results show that, associated with an increase in ERK2 activity, an epithelial to mesenchymal dedifferentiation occurred in both MDCK-C7F cells and caMEK1-transfected MDCK-C7 cells.
通过瞬时碱性应激去分化的MDCK - C7细胞(C7F细胞)或通过转染有丝分裂原活化蛋白激酶激酶MEK1的组成型活性突变体的MDCK - C7细胞(C7caMEK1细胞),采用蛋白质免疫印迹法和免疫荧光显微镜技术进行分析,以比较不同细胞角蛋白、波形蛋白和α - 平滑肌肌动蛋白的表达情况。与上皮野生型MDCK - C7细胞或mock转染的MDCK - C7细胞相比,在去分化细胞系C7F和C7caMEK1中,所有检测的细胞角蛋白,即II型中性和碱性细胞角蛋白CK5、CK7、CK8以及I型酸性角蛋白CK17和CK19的表达均显著降低。虽然在所检测的所有四种MDCK - C7细胞系中均检测到波形蛋白表达,但只有去分化细胞系C7F和C7caMEK1(据报道表达高活性ERK2)表现出含有α - 平滑肌肌动蛋白的应力纤维形成。综合我们的结果表明,与ERK2活性增加相关,MDCK - C7F细胞和caMEK1转染的MDCK - C7细胞均发生了上皮向间充质的去分化。