Seregina T M, Mekshenkov M I
Ontogenez. 1986 Sep-Oct;17(5):494-9.
The cells of the lymphoblastoid strain, RPMI-6410t (from the blood of a patient suffering an acute myeloblast leukemia), were shown to synthesize constitutively and secrete into the culture medium a growth factor that maintains the reproduction of these cells. The 6410t cells were shown to bind specifically this factor and react to it by proliferation in the conditions of rarefied inoculation. The utilization of a medium conditioned by the 6410t cells provided almost 100% cloning of these cells when using the method of limiting dilutions in 96-well microplates at a density of one cell per well. The cloning of the 6410t cells without the conditioned medium with feeder cells (mouse splenocytes and peritoneal cells) failed. It is suggested that as a result of the second stage of malignant transformation the immortalized cell still requires an exogenous growth factor, unlike was considered earlier, but acquires the ability of producing an endogenous growth factor and, hence, escapes the environmental control.
淋巴母细胞系RPMI - 6410t(源自一名急性髓母细胞白血病患者的血液)的细胞被证明可组成性合成一种生长因子,并分泌到培养基中,该生长因子能维持这些细胞的增殖。6410t细胞被证明可特异性结合这种因子,并在低密度接种条件下对其产生增殖反应。当在96孔微孔板中使用有限稀释法,以每孔一个细胞的密度接种时,利用6410t细胞条件培养基可使这些细胞几乎100%克隆。没有条件培养基和饲养细胞(小鼠脾细胞和腹腔细胞)时,6410t细胞的克隆失败。有人提出,与之前所认为的不同,作为恶性转化第二阶段的结果,永生化细胞仍然需要外源性生长因子,但获得了产生内源性生长因子的能力,因此摆脱了环境控制。