Okano H, Nishiyama T
Biomedicine. 1976 Dec 5;25(9):321-4.
Leukaemia cells of C12/0 line, derived from Gross virus-induced W/Fu rat thymoma, have been successfully maintained in a completely synthetic, serum-free RPMI 1640 medium. The cells propagated as good as in serum-supplemented medium, though they could not grow from a low cell density. Cells adhered to the substratum and did not survive. This problem was overcome by use of silicone-coated substratum, or of microexudate from C12/0 cells adsorbed on the substratum. The cells underwent degeneration soon after they reached their maximum density. C12/0 cells released macromolecules might possibly have both growth-promoting and toxic effect on the cell itself.
源自格罗斯病毒诱导的W/Fu大鼠胸腺瘤的C12/0系白血病细胞,已成功在完全合成的无血清RPMI 1640培养基中维持培养。这些细胞的增殖情况与在添加血清的培养基中一样好,不过它们无法从低密度状态开始生长。细胞会附着于基质但无法存活。通过使用硅酮包被的基质,或吸附在基质上的C12/0细胞的微分泌物,这一问题得到了克服。细胞在达到最大密度后不久就会发生退化。C12/0细胞释放的大分子可能对细胞自身既有促进生长的作用,也有毒性作用。