Lonai P, Declève A, Kaplan H S
Proc Natl Acad Sci U S A. 1974 May;71(5):2008-12. doi: 10.1073/pnas.71.5.2008.
Short-term lymphocyte cultures from mouse thymus, spleen, or lymph nodes were studied for the presence of murine leukemia virus group-specific antigens with an immunofluorescence test using rat immune sera against syngeneic cells infected with the radiation leukemia virus or its pseudotype of murine sarcoma virus and goat and rabbit antisera against purified murine leukemia virus group-specific antigen. Antigens reacting with these sera appeared in the cultured lymphocytes within 24 hr, and the proportion of immunofluorescent-positive cells increased to 25-80% by the second or third day of cultivation, concomitantly with a decrease in cell viability. The appearance of these antigens can be suppressed by inhibitors of DNA (mitomycin-C), RNA (actinomycin-D, cordycepin, and polyadenylic acid), and protein (cycloheximide) synthesis. No infectious virus could be detected by the immunofluorescence and XC-cell tests. The observed phenomenon appears to represent the spontaneous partial derepression of endogenous murine leukemia virus replication in lymphocytes during short-term in vitro cultivation.
利用大鼠免疫血清针对感染辐射白血病病毒或其鼠肉瘤病毒假型的同基因细胞,以及山羊和兔抗血清针对纯化的鼠白血病病毒群特异性抗原,通过免疫荧光试验研究了来自小鼠胸腺、脾脏或淋巴结的短期淋巴细胞培养物中鼠白血病病毒群特异性抗原的存在情况。与这些血清发生反应的抗原在培养的淋巴细胞中于24小时内出现,到培养的第二天或第三天,免疫荧光阳性细胞的比例增加到25% - 80%,与此同时细胞活力下降。这些抗原的出现可被DNA(丝裂霉素-C)、RNA(放线菌素-D、虫草素和聚腺苷酸)和蛋白质(环己酰亚胺)合成抑制剂所抑制。通过免疫荧光和XC细胞试验未检测到感染性病毒。观察到的现象似乎代表了在短期体外培养期间淋巴细胞内源性鼠白血病病毒复制的自发部分去抑制。