Stone L B, Takemoto K K
J Virol. 1970 Nov;6(5):621-7. doi: 10.1128/JVI.6.5.621-627.1970.
Studies were undertaken to prove that simian virus 40 (SV40) can transform the mouse macrophage, a cell type naturally restricted from deoxyribonucleic acid (DNA) replication. Balb/C macrophages infected with SV40 demonstrated T-antigen production and induced DNA synthesis simultaneously. In the absence of apparent division, these cells remained T antigen-positive for at least 45 days. SV40 could be rescued from nondividing, unaltered macrophages during the T antigen-producing period. Proliferating transformants appeared at an average of 66 days post-SV40 infection. Established cell lines were T antigen-positive and were negative for infectious virus, but yielded SV40 after fusion with African green monkey kidney cells. Their identity as transformed macrophages was substantiated by evaluation of cellular morphology, phagocytosis, acid phosphatase, beta(1c) synthesis, and aminoacridine incorporation.
开展了多项研究以证明猿猴病毒40(SV40)能够转化小鼠巨噬细胞,这是一种天然受限于脱氧核糖核酸(DNA)复制的细胞类型。感染SV40的Balb/C巨噬细胞表现出T抗原的产生并同时诱导DNA合成。在没有明显分裂的情况下,这些细胞在至少45天内保持T抗原阳性。在产生T抗原的时期,可以从未分裂、未改变的巨噬细胞中拯救出SV40。增殖性转化体平均在SV40感染后66天出现。建立的细胞系T抗原呈阳性且对传染性病毒呈阴性,但与非洲绿猴肾细胞融合后可产生SV40。通过对细胞形态、吞噬作用、酸性磷酸酶、β(1c)合成和氨基吖啶掺入的评估,证实了它们作为转化巨噬细胞的身份。