作者: Robert Langenbach , Carol Heckman , Eliezer Huberman
DOI:
关键词: Chemistry 、 Cellular differentiation 、 Phorbol 、 Stimulation 、 Cell growth 、 Molecular biology 、 Glucosamine 、 Cell culture 、 Biochemistry 、 Ganglioside 、 Dimethyl sulfoxide
摘要: Treatment of cultured human HO melanoma cells with the mouse skin tumor promoter phorbol-12-myristate-13-acetate (PMA) at 5 x 10/sup -10/ to -7/ M resulted in a dose-related inhibition growth and stimulation differentiated functions. These included melanin synthesis formation dendrite-like structues. Higher doses phorbol dibutyrate, less potent promoter, were required produce an effect comparable that PMA for dendrite induction. Phorbol two other phorbal esters, which lack tumor-promoting activity, either inactive or elicited poor response. In addition morphological changes, treatment altered glucosamine incorporation into membrane gangliosides. After treatment, increased 8- 10 fold G/sub m3/ ganglioside decreased 2-fold m1/ ganglioside, as compared untreated control. Inhibition cell also observed after dimethyl sulfoxide. Unlike agents, sulfoxide did not induce structures cells. findings indicate can be stimulated terminally agents such diesters.