We determined if we could transfer X-radiation resistance from CHO AA8
cells to their radiosensitive, mutant V3 cells by several methods. Th
ese methods include co-incubating the two cell lines for three days be
fore irradiation, adding heavily-irradiated AA8 to V3 cells following
irradiation of the latter and then co-incubating these cells for at le
ast eight days during the colony-forming assay and lastly, adding cond
itioned medium from unirradiated, subconfluent AA8 cells to V3 culture
s and incubating for two days before irradiation. None of these proced
ures enhanced the clonogenic survival of the V3 cells to a single dose
of 4 Gy X-radiation. Adding heavily-irradiated V3, instead of AA8, ce
lls did not increase the clonogenic survival of the 4 Gy-irradiated V3
cells either, indicating that there was no autocrine mode of action.
Moreover, adding conditioned medium from a related CHO cell line, K1,
to its own radiosensitive, mutant 5-11 and incubating for two days bef
ore irradiation did not enhance clonogenic survival of the latter to a
single dose of 3 Gy X-radiation. We therefore conclude that it is unl
ikely that CHO cells have the X-radiation resistance factor that has b
een reported in some mouse melanoma cell lines by other investigators.