Abstract:
:Immortalized retinal neurons have been established in tissue culture from retinal tumors arising in transgenic mice. The mice carry the SV40 T-antigen 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 proliferation population of T-antigen-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.
journal_name
Neuronjournal_title
Neuronauthors
Hammang JP,Baetge EE,Behringer RR,Brinster RL,Palmiter RD,Messing Adoi
10.1016/0896-6273(90)90204-ssubject
Has Abstractpub_date
1990-05-01 00:00:00pages
775-82issue
5eissn
0896-6273issn
1097-4199pii
0896-6273(90)90204-Sjournal_volume
4pub_type
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