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  The trk tyrosine protein kinase mediates the mitogenic properties of nerve growth factor and neurotrophin-3

Cordon-Cardo, C., Tapley, P., Jing, S. Q., Nanduri, V., Orourke, E., Lamballe, F., et al. (1991). The trk tyrosine protein kinase mediates the mitogenic properties of nerve growth factor and neurotrophin-3. Cell, 66(1), 173-183. doi:10.1016/0092-8674(91)90149-s.

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Cordon-Cardo, C., Author
Tapley, P., Author
Jing, S. Q., Author
Nanduri, V., Author
Orourke, E., Author
Lamballe, F., Author
Kovary, K., Author
Klein, Rüdiger1, Author           
Jones, K. R., Author
Reichardt, L. F., Author
Barbacid, M., Author
Affiliations:
1Bristol-Myers Squibb, Princeton, NJ, USA, ou_persistent22              

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Free keywords: factor ngf receptors molecular-cloning factor family gene-transfer high-affinity pc12 cells pheochromocytoma cells differentiation expression oncogene Biochemistry & Molecular Biology Cell Biology
 Abstract: The product of the trk proto-oncogene encodes a receptor for nerve growth factor (NGF). Here we show that NGF is a powerful mitogen that can induce resting NIH 3T3 cells to enter S phase, grow in semisolid medium, and become morphologically transformed. These mitogenic effects are absolutely dependent on expression of gp140trk receptors, but do not require the presence of the previously described low affinity NGF receptor. gp140trk also serves as a receptor for the related factor neurotrophin-3 (NT-3), but not for brain-derived neurotrophic factor. Both NGF and NT-3 induce the rapid phosphorylation of gp140trk receptors and the transient expression of c-Fos proteins. However, NT-3 appears to elicit more limited mitogenic responses than NGF. These results indicate that the product of the trk proto-oncogene is sufficient to mediate signal transduction processes induced by NGF and NT-3, at least in proliferating cells.

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Language(s): eng - English
 Dates: 1991-07-12
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: Other: WOS:A1991FW91300019
DOI: 10.1016/0092-8674(91)90149-s
ISSN: 0092-8674
 Degree: -

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Title: Cell
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 66 (1) Sequence Number: - Start / End Page: 173 - 183 Identifier: ISSN: 0092-8674
CoNE: https://pure.mpg.de/cone/journals/resource/954925463183