Investigative ophthalmology & visual science · 1994
Photoreceptor cell tumors in transgenic mice.
СтатьяПоддержка исследования: вне правительства СШАПоддержка службы здравоохранения СШАНазвание и аннотация: Перевод пока не подготовлен
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Howes K A, Lasudry J G, Albert D M, Windle J J
Аннотация
PURPOSE: To produce transgenic mice that express the SV40 T-antigen oncogene specifically in photoreceptor cells, giving rise to retinoblastoma tumors of photoreceptor cell origin; to characterize the mice with regard to transgene expression and pathology and to characterize the resulting tumors histologically.
METHODS: Transgenic mice were generated that express T-antigen under the control of the murine interstitial retinol binding protein promoter.
RESULTS: All mice produced developed either ocular or intracranial tumors, or both, at an early age. One line of mice was generated, and all mice of this line develop both retinal photoreceptor cell and pineal tumors by as early as 2 weeks of age. Cell lines have been established from both tumor types.
CONCLUSIONS: These mice represent an animal model system for human trilateral retinoblastoma, in which retinoblastomas are accompanied by pineal tumors.
METHODS: Transgenic mice were generated that express T-antigen under the control of the murine interstitial retinol binding protein promoter.
RESULTS: All mice produced developed either ocular or intracranial tumors, or both, at an early age. One line of mice was generated, and all mice of this line develop both retinal photoreceptor cell and pineal tumors by as early as 2 weeks of age. Cell lines have been established from both tumor types.
CONCLUSIONS: These mice represent an animal model system for human trilateral retinoblastoma, in which retinoblastomas are accompanied by pineal tumors.
Предметные рубрики MeSH
AnimalsAntigens, Polyomavirus TransformingBlotting, NorthernBrain NeoplasmsDisease Models, AnimalEye NeoplasmsEye ProteinsFemaleGene ExpressionMaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicPhotoreceptor CellsPineal GlandRetinoblastomaRetinol-Binding ProteinsTumor Cells, CulturedRetinol-Binding Proteins, Interstitial