Variant (MDCK) kidney epithelial cells altered in response to inducers of dome formation and differentiation
- 1 January 1985
- journal article
- research article
- Published by Wiley in Journal of Cellular Physiology
- Vol. 122 (1), 45-52
- https://doi.org/10.1002/jcp.1041220108
Abstract
Confluent cultures of the MDCK kidney epithelial cell line exhibit dome formation, a result of transepithelial fluid transport influenced by cell-cell and cell-substratum interaction. Dome formation was inducible by hexamethylene bisacetamide (HMBA) or dimmethylformamide (DMF), compounds known as inducers of cell differentiation (Lever, 1979b). Analysis of the incidence of the dome-forming phenotype in colonies derived nonselectively from the MDCK cell line suggested that inducers recruit an increased fraction of the cell population to express dome formation. Variant MDCK cell lines were isolated which differed from the parental line in response to inducers while retaining cuboidal epithelial morphology. In five independently isolated and cloned MDCK variants, dome formation was not inducible by DMF and only marginally increased by HMBA. This phenotype was also associated with increased cell adhesiveness to a plastic substratum. Results from cocultivation experiments suggested that the DMF-unresponsive phenotype of variant cells may be partially overcome by cell-cell contact with wild-type cells. Sodium pump transport activity assessed by ouabain-sensitive Rb+ uptake was partially inhibited by HMBA and by DMF in a “wild-type” inducer-responsive clone. By contrast, DMF did not inhibit ouabain-sensitive Rb+ uptake in DMF-unresponsive variant clones, and sodium pump inhibition by HMBA was greatly diminished. This close correspondence between altered sodium pump modulation by inducers in variant clones and their altered dome-forming response reinforces our previous conclusions (Kennedy and Lever, 1984) that sodium pump modulation is closely associated with mechanisms of inducer action. Taken together, these findings implicate cell-cell interaction, cell-substratum interaction and sodium pump modulation in regulation of the differentiated phenotype of this cell line.This publication has 32 references indexed in Scilit:
- Regulation of Na+, K+‐ATPase activity in MDCK kidney epithelial cell cultures: Role of growth state, cyclic AMP, and chemical inducers of dome formation and differentiationJournal of Cellular Physiology, 1984
- PGE1-independent MDCK cells have elevated intracellular cyclic AMP but retain the growth stimulatory effects of glucagon and epidermal growth factor in serum-free mediumJournal of Cellular Physiology, 1984
- Loss of the PGE1 requirement for MDCK cell growth associated with a defect in cyclic AMP phosphodiesteraseJournal of Cellular Physiology, 1983
- Stimulation of dome formation in MDCK kidney epithelial cultures by inducers of differentiation: Dissociation from effects on transepithelial resistance and cyclic AMP levelsJournal of Cellular Physiology, 1982
- The MDCK epithelial cell line expresses a cell surface antigen of the kidney distal tubule.The Journal of cell biology, 1982
- MORPHOLOGICAL SIMILARITIES BETWEEN THE DOG KIDNEY CELL LINE MDCK AND THE MAMMALIAN CORTICAL COLLECTING TUBULE*Annals of the New York Academy of Sciences, 1981
- Ion transport in ‘tight’ epithelial monolayers of MDCK cellsThe Journal of Membrane Biology, 1981
- Alterations in growth requirements of kidney epithelial cells in defined medium associated with malignant transformationJournal of Supramolecular Structure and Cellular Biochemistry, 1981
- Distribution and characteristics of the occluding junctions in a monolayer of a cell line (MDCK) derived from canine kidneyThe Journal of Membrane Biology, 1978
- The program of friend cell erythroid differentiation: Early changes in Na+/K+ ATPase functionJournal of Supramolecular Structure, 1978