Sonobe H
Acta Med Okayama. 1976 Jun;30(3):163-79.
Human adenovirus type 12 (Ad 12) was inoculated through subtentorial route into inbred newborn mice (C3H/BifB/Ki), and sequential changes of the brain and tumor induction were examined by histological and immunofluorescent methods. Two days after virus inoculation, Ad 12 specific tumor antigen (fluorescent T-antigen) appeared in the cells of ependymal and subventricular matrix layers, choroid plexuses and leptomeninges in the subtentorial as well as the supratentorial brains. After 10 days, these fluorescent positive cells decreased gradually in number but still remained focally beneath the ependyma. Sixty days later, early tumor nodules were detected in the same regions in which remained the fluorescent cells. After 107 days, neurological signs and well-developed tumors were noted in 25 of 63 (30.1%) mice examined. In the cerebellum, both of T-antigens and tumors were limited around the IVth ventricle, but not in the granular layers. Histomorphologically, the tumors were of primitive neuroectodermal origin and consisted of the cells resembling immature matrix cells in the subventricular zone. These findings strongly suggest that the virus has a selective affinity to the remaining matrix cells, but not to cerebellar granular cells, at least, in newborn mice.
将12型人腺病毒(Ad 12)经幕下途径接种到近交系新生小鼠(C3H/BifB/Ki)体内,通过组织学和免疫荧光方法检查脑的连续变化和肿瘤诱导情况。病毒接种两天后,Ad 12特异性肿瘤抗原(荧光T抗原)出现在幕下和幕上脑室内的室管膜和室下基质层、脉络丛和软脑膜的细胞中。10天后,这些荧光阳性细胞数量逐渐减少,但仍局部保留在室管膜下方。60天后,在仍保留荧光细胞的相同区域检测到早期肿瘤结节。107天后,在检查的63只小鼠中有25只(30.1%)出现神经症状和发育良好的肿瘤。在小脑中,T抗原和肿瘤都局限于第四脑室周围,但颗粒层未出现。组织形态学上,肿瘤起源于原始神经外胚层,由类似于室下区未成熟基质细胞的细胞组成。这些发现强烈表明,至少在新生小鼠中,该病毒对残留的基质细胞具有选择性亲和力,而对小脑颗粒细胞没有亲和力。