Nicolson M O, Gilden R V, Charman H, Rice N, Heberling R, McAllister R M
Int J Cancer. 1978 Jun 15;21(6):700-6. doi: 10.1002/ijc.2910210606.
DNA was extracted from two human sarcoma cell lines, TE-32 and TE-418, and the leukemic cells from five children with acute myelocytic leukemia, three children with acute lymphocytic leukemia and four adults with acute myelocytic leukemia. The DNAs, assayed for infectivity by transfection techniques, induced no measurable virus by methods which would detect known mammalian C-type antigens or RNA-directed DNA polymerase in TE-32, D-17 dog cells and other indicator cells, nor did they recombine with or rescue endogenous human or exogenous murine or baboon type-C virus. Model systems used as controls were human sarcoma cells, TE-32 and HT-1080, and human lymphoma cells TE-543, experimentally infected with KiMuLV, GaLV or baboon type-C virus, all of which released infectious virus and whose DNAs were infectious for TE-32 and D-17 dog cells. Other model systems included two baboon placentas and one embryonic cell strain spontaneously releasing infectious endogenous baboon virus and yielding DNAs infectious for D-17 dog cells but not for TE-32 cells. Four other baboon embryonic tissues and two embryonic cell strains, releasing either low levels of virus or no virus, did not yield infectious DNA.
从两个人类肉瘤细胞系TE - 32和TE - 418以及五名急性髓细胞白血病儿童、三名急性淋巴细胞白血病儿童和四名急性髓细胞白血病成人的白血病细胞中提取了DNA。通过转染技术检测感染性的这些DNA,在TE - 32、D - 17狗细胞和其他指示细胞中,用能检测已知哺乳动物C型抗原或RNA指导的DNA聚合酶的方法未检测到可测量的病毒,它们也未与内源性人类或外源性鼠类或狒狒C型病毒重组或拯救这些病毒。用作对照的模型系统是用人肉瘤细胞TE - 32和HT - 1080以及人淋巴瘤细胞TE - 543,它们经实验感染了KiMuLV、GaLV或狒狒C型病毒,所有这些细胞都释放出感染性病毒,且其DNA对TE - 32和D - 17狗细胞具有感染性。其他模型系统包括两个狒狒胎盘和一个自发释放感染性内源性狒狒病毒并产生对D - 17狗细胞具有感染性但对TE - 32细胞无感染性的DNA的胚胎细胞系。另外四个狒狒胚胎组织和两个胚胎细胞系,要么释放低水平的病毒,要么不释放病毒,未产生感染性DNA。