Schellekens H, De Wilde G A, Weimar W
J Gen Virol. 1980 Jan;46(1):243-7. doi: 10.1099/0022-1317-46-1-243.
Rat interferon of relatively high specific activity (about 10(6) units/mg protein) was produced in embryonic rat cells treated with Newcastle disease virus at a high m.o.i. The cells were cultured in serum-free medium and the interferon was precipitated and concentrated with 0.02 M-zinc acetate or with ammonium sulphate at 85% saturation. With both methods the increase in interferon activity was greater than the concentration factor. The rat interferon activity was stable on treatment with 0.15 M-perchloric acid or three cycles of freezing and thawing, but incubation at 37 degrees C for 1 h resulted in a 50% loss in activity. It had no cross activity in human or mouse cells. The sensitivity of different types of rat cells for rat interferon differed widely and was dependent on the challenge virus. Human interferons had no detectable antiviral activity on rat cells and did not block the activity of rat interferon.
在高感染复数下用新城疫病毒处理的胚胎大鼠细胞中产生了具有相对较高比活性(约10⁶单位/毫克蛋白质)的大鼠干扰素。细胞在无血清培养基中培养,干扰素用0.02M乙酸锌或85%饱和度的硫酸铵沉淀并浓缩。两种方法中,干扰素活性的增加都大于浓缩系数。大鼠干扰素活性在用0.15M高氯酸处理或三个冻融循环后稳定,但在37℃孵育1小时导致活性损失50%。它在人或小鼠细胞中无交叉活性。不同类型的大鼠细胞对大鼠干扰素的敏感性差异很大,并且取决于攻击病毒。人干扰素在大鼠细胞上没有可检测到的抗病毒活性,也不阻断大鼠干扰素的活性。