Smith T J, Wagner R R
J Exp Med. 1967 Apr 1;125(4):579-93. doi: 10.1084/jem.125.4.579.
Antiviral factors present in cultures of rabbit peritoneal macrophages or rabbit kidney (RK) cells infected with Newcastle disease virus (NDV) and those in cultures of uninfected macrophages all fulfilled the biological and physicochemical criteria for classification as interferons. Virus-induced macrophage and RK interferons were slightly more stable to heat or acid than "spontaneously produced" or endotoxin-induced macrophage interferon. Interferon activity in serum of NDV-infected rabbits was decidedly more labile than NDV-induced macrophage interferon. However, these differences in lability were too slight to serve as a useful basis for distinguishing one rabbit interferon from another. Rabbit interferons from various sources could be differentiated by filtration through Sephadex G-100 and their molecular weights estimated by comparison with elution profiles of a series of marker proteins of known molecular weight. Each of four different preparations of rabbit interferons was found to contain more than one molecular component. Elution peaks for three NDV-induced interferons were equivalent to the following molecular weights: RK approximately 44,000-45,000 and > 134,000 (variable and < 1% when present); macrophage approximately 37,000, 44,000-45,000, and > 134,000 (variable and <1% when present); and serum approximately 50,000-52,000 and > 134,000 ( approximately 10% and heat labile). NDV-induced serum interferon may also contain another molecular component of mol wt approximately 45,000 represented by a trailing shoulder from the major 51,000 mol wt peak. Endotoxin-induced macrophage interferon proved to be polydisperse. Sephadex filtration of this interferon did not reveal clear and consistent elution patterns, partially owing to its low initial titer and lability. However, variable peaks of biological activity could be detected in Sephadex fractions equivalent to approximate molecular weight values of > 134,000, 72,000-78,000, 33,000-38,000, 28,000-30,000, and possibly a component of 42,000-45,000. A major component of mol wt approximately 37,000 was present in all samples of endotoxin-induced macrophage interferon. The other constituents may be biologically active subunits or polymers. These data indicate that rabbit macrophages produce two primary kinds of interferon: (a) an RK-like component of mol wt approximately 45,000 that is synthesized in greatest amount after viral induction, and (b) a different species of mol wt approximately 37,000 that can also be synthesized in the absence of viral induction. The presence of major interferon constituents of mol wt approximately 51,000 and > 134,000 in rabbit serum after viral induction suggests that macrophages are not the principal interferon-producing cells that respond to intravenous injection of NDV.
感染新城疫病毒(NDV)的兔腹膜巨噬细胞或兔肾(RK)细胞培养物中存在的抗病毒因子,以及未感染巨噬细胞培养物中的抗病毒因子,均符合作为干扰素分类的生物学和物理化学标准。病毒诱导的巨噬细胞和RK干扰素比“自发产生的”或内毒素诱导的巨噬细胞干扰素对热或酸的稳定性略高。感染NDV的兔血清中的干扰素活性比NDV诱导的巨噬细胞干扰素明显更不稳定。然而,这些稳定性的差异太小,无法作为区分一种兔干扰素与另一种兔干扰素的有用依据。来自各种来源的兔干扰素可以通过Sephadex G - 100过滤进行区分,并通过与一系列已知分子量的标记蛋白的洗脱图谱比较来估计其分子量。发现四种不同的兔干扰素制剂中的每一种都含有不止一种分子成分。三种NDV诱导的干扰素的洗脱峰相当于以下分子量:RK约为44,000 - 45,000和> 134,000(存在时可变且<1%);巨噬细胞约为37,000、44,000 - 45,000和> 134,000(存在时可变且<1%);血清约为50,000 - 52,000和> 134,000(约10%且对热不稳定)。NDV诱导的血清干扰素可能还含有另一种分子量约为45,000的分子成分,由主要的51,000分子量峰的拖尾峰表示。内毒素诱导的巨噬细胞干扰素被证明是多分散的。这种干扰素的Sephadex过滤未显示出清晰一致的洗脱模式,部分原因是其初始滴度低且不稳定。然而,在相当于分子量> 134,000、72,000 - 78,000、33,000 - 38,000、28,000 - 30,000以及可能42,000 - 45,000的Sephadex级分中可以检测到可变的生物活性峰。内毒素诱导的巨噬细胞干扰素的所有样品中都存在一种分子量约为37,000的主要成分。其他成分可能是生物活性亚基或聚合物。这些数据表明兔巨噬细胞产生两种主要类型的干扰素:(a)一种分子量约为45,000的类似RK的成分,在病毒诱导后合成量最大,以及(b)一种不同的分子量约为37,000的类型,在没有病毒诱导的情况下也可以合成。病毒诱导后兔血清中存在分子量约为51,000和> 134,000的主要干扰素成分,这表明巨噬细胞不是对静脉注射NDV作出反应的主要干扰素产生细胞。