IMMORTALIZED RETINAL NEURONS DERIVED FROM SV40 T-ANTIGEN-INDUCED TUMORS IN TRANSGENIC MICE

被引:79
作者
HAMMANG, JP
BAETGE, EE
BEHRINGER, RR
BRINSTER, RL
PALMITER, RD
MESSING, A
机构
[1] BRISTOL MYERS SQUIBB CO,CNS BIOL,WALLINGFORD,CT 06492
[2] UNIV PENN,SCH VET MED,REPROD PHYSIOL LAB,PHILADELPHIA,PA 19104
[3] UNIV WASHINGTON,HOWARD HUGHES MED INST,DEPT BIOCHEM,SEATTLE,WA 98195
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0896-6273(90)90204-S
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Immortalized retinal neurons have been established in tissue culture from retinal tumors arising in transgenic mice. The mice carry the SV40 Tantigen under the control of 5′ flanking sequences from the human phenylethanolamine N-methyltransferase (PNMT) gene in order to target oncogene expression to adrenergic cell types. The retinal cultures contain a proliferating population of Tantigen-positive cells with a neuronal morphology that includes formation of extensive neuritic processes. We identified the cells as amacrine-derived neurons by immunofluorescence using the cell-specific monoclonal antibodies VC1.1 and HPC-1. The cells also express all three neurofilament subunits and GAP-43. These results indicate that CNS neurons can be transformed in transgenic animals to generate cultured cells with many properties of mature neurons. © 1990.
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页码:775 / 782
页数:8
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