Summary
Cells were isolated from tissue fragments of the Harding-Passey-melanoma of a NMRI-mouse and cultivated in monolayer cell culture since 3 years. These cells have maintained the capability to produce melanin. The culture medium consisted of Eagle’s basal medium supplemented with 10% fetal calf serum. The cells were subcultivated 30 times, so far. The average population doubling-time was about 100 hours.
29 out of 75 inoculated mice developed solid, not-metastasizing, melanotic tumors after subcutaneous injection of culture cells.
Proliferating cell-cultures contained little melanin; however the melanin content strongly increased with increasing cell density and decreasing cell proliferation-rate.
Possible relationships between inhibition of cell multiplication and “initiation” of a specific cell function (melanin-synthesis) were discussed.
Zusammenfassung
Aus Gewebefragmenten eines Harding-Passey-Melanoms einer NMRI-Maus wurden Zellen isoliert und seit 3 Jahren in Monolayer-Zellkultur unter Erhalt der Fähigkeit zur Melaninsynthese weitergezüchtet. Als Nährmedium diente Eagle’s Basal-medium, welches mit 10% fetalem Kalbsserum ergänzt wurde. Die Zellen wurden bisher 30mal subkultiviert. Die durchschnittliche Verdopplungszeit betrug etwa 100 Std.
Nach subcutaner Injektion von Kulturzellen entwickelten sich bei 29 von 75 inoculierten Mäusen solide, nicht-metastasierende, melanotische Tumoren.
Kulturen von proliferierenden Zellen enthielten wenig Melanin; dagegen stieg der Melaningehalt bei zunehmender Zelldichte und verminderter Vermehrungsgeschwindigkeit stark an.
Mögliche Zusammenhänge zwischen Hemmung der Zellvermehrung und Ausprägung einer spezifischen Zellfunktion (Melaninsynthese) wurden diskutiert.
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Mit Untersützung der Deutschen Forschungsgemeinschaft (Scha 176/1 und 176/2).
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Schachtschabel, D. Spezifische Zellfunktionen von Zell- und Gewebekulturen. Virchows Arch. Abt. B Zellpath. 7, 27–36 (1971). https://doi.org/10.1007/BF02892076
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DOI: https://doi.org/10.1007/BF02892076