Faculty Research 1990 - 1999
The combination of epidermal growth factor and transforming growth factor-beta induces novel phenotypic changes in mouse liver stem cell lines.
Document Type
Article
Publication Date
1997
Keywords
Cell-Line, Epidermal-Growth-Factor, Kinetics, Liver, Mice, Mitogens, Phenotype, Signal-Transduction, Stem-Cells, Transforming-Growth-Factor-beta
First Page
3117
Last Page
3129
JAX Source
J Cell Sci 1997 Dec; 110(pt24):3117-29.
Abstract
Mouse liver stem cell (oval cell) lines were investigated in order to determine the role which two families of growth and differentiation factors (GDFs), epidermal growth factor (EGF) family and transforming growth factor beta (TGF-beta) family, play in liver regeneration. EGF family members, including EGF, amphiregulin, betacellulin, heparin-binding epidermal growth factor, and TGF-alpha, were mitogenic for oval cell lines while TGF-beta family members, including TGF-beta1, TGF-beta2 and TGF-beta3, inhibited mitogenesis and induced apoptosis in oval cell lines. Surprisingly, the combination of EGF family members and TGF-ss family members resulted in neither proliferation nor apoptosis but instead in a novel cellular response, cellular scattering in tissue culture and morphological differentiation in Matrigel. Analysis of the signal transduction pathways activated by exposure of oval cell lines to either EGF, EGF+TGF-beta, or TGF-beta indicated that novel combinations of intracellular signals result following stimulation of the cells with the combination of EGF+TGF-beta. These data reveal that the dynamics of synergistic GDF action following tissue injury and regeneration results in a new level of complexity not obvious from the study of individual GDFs.
Recommended Citation
Isfort RJ,
Cody DB,
Stuard SB,
Randall CJ,
Miller C,
Ridder GM,
Doersen CJ,
Richards WG,
Yoder BK,
Wilkinson JE,
Woychik RP.
The combination of epidermal growth factor and transforming growth factor-beta induces novel phenotypic changes in mouse liver stem cell lines. J Cell Sci 1997 Dec; 110(pt24):3117-29.