Levy R L, Lerner R A, Dixon F J
Cancer Res. 1976 Jun;36(6):2090-5.
Infection of adult BALB/c mice with murine leukemia virus (MuLV) induces thymic lymphomas histologically indistinguishable from those caused by neonatal infection. X-irradiation permitted early and high levels of viral expression when given before or after MuLV administration and hastened the development of lymphomas. Expression of virus was assayed by using a radioimmune assay for murine p30, a virion core protein. Seventeen to 21 days after injection of MuLV into adult mice, there was 0.3 mug p30 per ml serum, approximately 5 times normal. Seventeen to 21 days after injection of MuLV into X-irradiated (600R) adult mice, there were 2.7 mug p30 per ml serum. The virus produced by infected adult mice was infectious and oncogenic when given to newborn mice.
用鼠白血病病毒(MuLV)感染成年BALB/c小鼠可诱发组织学上与新生小鼠感染所致淋巴瘤无法区分的胸腺淋巴瘤。在给予MuLV之前或之后进行X射线照射可使病毒早期高水平表达,并加速淋巴瘤的发展。通过针对鼠p30(一种病毒体核心蛋白)的放射免疫测定法检测病毒表达。将MuLV注射到成年小鼠体内17至21天后,血清中每毫升有0.3微克p30,约为正常水平的5倍。将MuLV注射到经X射线照射(600伦琴)的成年小鼠体内17至21天后,血清中每毫升有2.7微克p30。感染成年小鼠产生的病毒在给予新生小鼠时具有传染性和致癌性。