Involvement of ras p21 protein in signal-transduction pathways from interleukin 2, interleukin 3, and granulocyte/macrophage colony-stimulating factor, but not from interleukin 4.
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- T Satoh
- DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, CA 94304-1104.
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- M Nakafuku
- DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, CA 94304-1104.
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- A Miyajima
- DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, CA 94304-1104.
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- Y Kaziro
- DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, CA 94304-1104.
抄録
<jats:p>The protooncogene ras acts as a component of signal-transduction networks in many kinds of cells. The ras gene product (p21) is a GTP-binding protein, and the activity of the protein is regulated by bound GDP/GTP. Recent studies have shown that a certain class of growth factors stimulates the formation of active p21-GTP complexes in fibroblasts and that oncogene products with enhanced tyrosine kinase activities have a similar effect on ras p21. We have measured the ratio of active GTP-bound p21 to total p21 in several lymphoid and myeloid cell lines in order to understand the role of ras in the proliferation of these cells. Interleukin 2 (IL-2), IL-3, and granulocyte/macrophage colony-stimulating factor (GM-CSF) enhance the formation of the active p21.GTP, whereas IL-4 has no effect on p21-bound GDP/GTP. These results strongly suggest that ras p21 acts as a transducer of signals from IL-2, IL-3, and GM-CSF, but not from IL-4.</jats:p>
収録刊行物
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- Proceedings of the National Academy of Sciences
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Proceedings of the National Academy of Sciences 88 (8), 3314-3318, 1991-04-15
Proceedings of the National Academy of Sciences
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詳細情報 詳細情報について
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- CRID
- 1361981470745709824
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- NII論文ID
- 80005845868
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- ISSN
- 10916490
- 00278424
- http://id.crossref.org/issn/00278424
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