Whyte P F, Subramaniam R, Hudson J B
Division of Medical Microbiology, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
Arch Virol. 1987;96(3-4):169-83. doi: 10.1007/BF01320958.
Murine cytomegalovirus infection in spleen cultures resulted in the production of a soluble factor, VISF (virus-induced suppressive factor), which inhibited concanavalin A mitogenesis in fresh spleen cells. Its production was specific for MCMV, since infection of spleen cultures by Sindbis virus, or bacteriophages PM 2 and T 4, and the phagocytosis of latex beads, all failed to elicit VISF. Maximum appearance of the factor occurred within 24 hours p.i. in spleen cultures, and its source was identified as the population of spleen cells which adhered to a plastic culture dish within two hours at 37 degrees C. Non-adherent cells did not produce the factor. Its production was not inhibited by indomethacin. VISF could be concentrated by ultrafiltration on a YM 2 membrane filter, and it was readily fractionated by chromatography on sephadex G-25. In relation to peptides of known molecular weight it appeared to be smaller than 1,400 daltons. Its ability to suppress concanavalin A mitogenesis was largely removed by digestion with proteinase K. Thus VISF appears to be a relatively small peptide or peptide-containing substance. It was purified further by HPLC.
脾脏培养物中的小鼠巨细胞病毒感染导致产生一种可溶性因子,即病毒诱导抑制因子(VISF),它能抑制新鲜脾细胞中伴刀豆球蛋白A的有丝分裂。它的产生是巨细胞病毒特有的,因为辛德毕斯病毒、噬菌体PM 2和T 4感染脾脏培养物以及乳胶珠的吞噬作用均未能引发VISF。该因子在感染后24小时内在脾脏培养物中达到最大量,其来源被确定为在37摄氏度下两小时内附着于塑料培养皿的脾细胞群体。未附着的细胞不产生该因子。消炎痛不抑制其产生。VISF可通过在YM 2膜过滤器上超滤进行浓缩,并且很容易通过在葡聚糖G - 25上进行色谱分离。与已知分子量的肽相比,它似乎小于1400道尔顿。用蛋白酶K消化后,其抑制伴刀豆球蛋白A有丝分裂的能力基本丧失。因此,VISF似乎是一种相对较小的肽或含肽物质。它通过高效液相色谱法进一步纯化。