Ryder E F, Snyder E Y, Cepko C L
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
J Neurobiol. 1990 Mar;21(2):356-75. doi: 10.1002/neu.480210209.
Neural cell lines were produced by retroviral vector-mediated transduction of the avian myc oncogene. Target cells were mitotic progenitor cells of postnatal mouse olfactory bulb and cerebellum, and postnatal rat cerebral cortex. Infection of the first two areas, where neurogenesis and gliogenesis occur postnatally, produced multipotent clonal lines that exhibited phenotypes of both neuronal and glial cells, and one line with a stable neuronal phenotype. Infection of cerebral cortex, where gliogenesis, but not neurogenesis, occurs postnatally, generated mortal clones that exhibited cells of glial phenotype. These lines should prove valuable for both in vitro and in vivo studies aimed at understanding the control of cell fate and differentiation of neural progenitors.
通过逆转录病毒载体介导的禽源myc癌基因转导产生了神经细胞系。靶细胞是出生后小鼠嗅球和小脑以及出生后大鼠大脑皮层的有丝分裂祖细胞。对出生后发生神经发生和胶质发生的前两个区域进行感染,产生了表现出神经元和胶质细胞两种表型的多能克隆系,以及一个具有稳定神经元表型的细胞系。对出生后发生胶质发生但不发生神经发生的大脑皮层进行感染,产生了表现出胶质细胞表型细胞的有限克隆。这些细胞系对于旨在了解神经祖细胞的细胞命运控制和分化的体外和体内研究都应具有重要价值。