Blalock J E
Infect Immun. 1979 Feb;23(2):496-501. doi: 10.1128/iai.23.2.496-501.1979.
The rate and degree of interferon action on mouse embryo (ME), mouse L, and human amnion (WISH) cells were found to be dependent on the cell density. The most precipitous drop in interferon action occurred just below cell confluency. This effect was shown with both vesicular stomatitis virus and Sindbis virus and at both constant and variable input multiplicities of infection. At both "high" and "low" cell densities, cells attached to a surface develop viral resistance faster than suspended cells. These data indicate that either cell contact or close cell proximity is required for maximal interferon activity. These results are discussed in relation to interferon-induced transfer of viral resistance.
研究发现,干扰素对小鼠胚胎(ME)细胞、小鼠L细胞和人羊膜(WISH)细胞的作用速率和程度取决于细胞密度。干扰素作用最急剧的下降发生在细胞接近汇合时。无论是水泡性口炎病毒还是辛德毕斯病毒,在恒定和可变的感染输入复数下均显示出这种效应。在“高”和“低”细胞密度下,贴附于表面的细胞比悬浮细胞更快产生抗病毒抗性。这些数据表明,最大干扰素活性需要细胞接触或细胞紧密相邻。结合干扰素诱导的抗病毒抗性转移对这些结果进行了讨论。