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Regulation of the differentiation of PC12 pheochromocytoma cells.
Author(s) -
Kanna Fujita,
Philip Lazarovici,
Gordon Guroff
Publication year - 1989
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.8980127
Subject(s) - nerve growth factor , adrenal medulla , pheochromocytoma , microbiology and biotechnology , cytoplasm , transcription factor , biology , clone (java method) , cellular differentiation , nucleus , cell culture , gene expression , gene , neuroscience , endocrinology , receptor , genetics , catecholamine
The PC12 clone, developed from a pheochromocytoma tumor of the rat adrenal medulla, has become a premiere model for the study of neuronal differentiation. When treated in culture with nanomolar concentrations of nerve growth factor, PC12 cells stop dividing, elaborate processes, become electrically excitable, and will make synapses with appropriate muscle cells in culture. The changes induced by nerve growth factor lead to cells that, by any number of criteria, resemble mature sympathetic neurons. These changes are accompanied by a series of biochemical alterations occurring in the membrane, the cytoplasm, and the nucleus of the cell. Some of these events are independent of changes in transcription, while others clearly involve changes in gene expression. A number of the alterations seen in the cells involve increases or decreases in the phosphorylation of key cellular proteins. The information available thus far allows the construction of a hypothesis regarding the biochemical basis of PC12 differentiation.

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