Fraser H
Food Chem Toxicol. 1986 Feb;24(2):105-11. doi: 10.1016/0278-6915(86)90344-3.
In a survey of 75,000 brains from 23 inbred mouse strains studied during research work on scrapie, astrocytoma was by far the commonest neuroectodermal tumour. It occurred in VM and BRVR mice at a 1% incidence, but was virtually absent from other strains. In VM mice it occurred nearly twice as often in males as in females, sometimes causing neurological signs of circling, depression or spinal paralysis, but more often showing no clinical effects and being discovered only during routine neuropathology carried out for other purposes. Astrocytomas occurred in mice in the spinal cord or in the brain, with equal frequency in the fore-, mid- and hindbrain. A dual origin has never been confirmed, but astrocytomas occasionally co-existed with other central nervous system tumours. Macroscopically they cause no distortion of the brain; this contrasts with the rare oligodendroglioma, in cases of which the brain is sometimes swollen and misshapen. Astrocytomas characteristically spread through white-matter tracts, but in some grey-matter localities neoplastic astrocytes can co-exist with viable neurons, suggesting that they may subserve some functions of normal astrocytes. The astrocytomas found in this study often co-existed with scrapie lesions. Scrapie-induced vacuolation penetrated some astrocytomas in grey matter, and the specific scrapie-associated argyrophilic (amyloid) plaques occurred in the middle of an astrocytoma in several mice. However, there is no relationship between the occurrence of astrocytoma and scrapie infection, and the neoplasm also occurs independently both of the Sinc gene, which controls the pathogenesis of scrapie, and of the histocompatibility type of the strains concerned. The spontaneous VM astrocytoma is transplantable intracerebrally and, in the early series of in vivo subpassages, it only grew in the brains of mice of the strain of origin and its crosses. The age occurrence of astrocytoma and the incidence of other CNS tumours in mice are discussed in this paper.
在对23种近交系小鼠进行羊瘙痒病研究工作期间所检测的75000个大脑中,星形细胞瘤是迄今为止最常见的神经外胚层肿瘤。它在VM和BRVR小鼠中的发生率为1%,但在其他品系中几乎不存在。在VM小鼠中,雄性的发生率几乎是雌性的两倍,有时会引起转圈、抑郁或脊髓麻痹等神经症状,但更常见的是没有临床症状,仅在为其他目的进行的常规神经病理学检查中被发现。星形细胞瘤发生在小鼠的脊髓或大脑中,在前脑、中脑和后脑的发生率相同。虽然从未证实其具有双重起源,但星形细胞瘤偶尔会与其他中枢神经系统肿瘤同时存在。从宏观上看,它们不会导致大脑变形;这与罕见的少突胶质细胞瘤形成对比,在少突胶质细胞瘤病例中,大脑有时会肿胀且形状异常。星形细胞瘤的特征是通过白质束扩散,但在一些灰质区域,肿瘤性星形胶质细胞可以与存活的神经元共存,这表明它们可能承担了正常星形胶质细胞的一些功能。在本研究中发现的星形细胞瘤通常与羊瘙痒病病变同时存在。羊瘙痒病引起的空泡化穿透了一些灰质中的星形细胞瘤,并且在几只小鼠的星形细胞瘤中间出现了与羊瘙痒病相关的特异性嗜银(淀粉样)斑块。然而,星形细胞瘤的发生与羊瘙痒病感染之间没有关系,并且这种肿瘤也独立于控制羊瘙痒病发病机制的Sinc基因以及相关品系的组织相容性类型而发生。自发性VM星形细胞瘤可在脑内移植,在早期的体内传代系列中,它只在起源品系及其杂交后代的小鼠脑中生长。本文讨论了小鼠星形细胞瘤的年龄分布情况以及其他中枢神经系统肿瘤的发生率。