Potassium channel induction by the Ras/Raf signal transduction cascade

• Published in: The Journal of biological chemistry Vol. 269; no. 49; pp. 31183 - 31189
• Main Authors: Huang, Y, Rane, S G
• Format: Journal Article
• Language: English
• Published: United States American Society for Biochemistry and Molecular Biology 09.12.1994
• Subjects: 3T3 Cells; Animals; Cell Division; Cell Line, Transformed; Charybdotoxin; Cyclic AMP-Dependent Protein Kinases - metabolism; Epidermal Growth Factor - physiology; Mice; Mice, Inbred C3H; Platelet-Derived Growth Factor - physiology; Potassium Channel Blockers; Potassium Channels - drug effects; Potassium Channels - physiology; Protein Kinase C - metabolism; Protein-Serine-Threonine Kinases - physiology; Proto-Oncogene Proteins - physiology; Proto-Oncogene Proteins c-raf; Quaternary Ammonium Compounds - pharmacology; ras Proteins - physiology; Scorpion Venoms - pharmacology; Signal Transduction
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(18)47407-8

p21ras plays a critical role in cell growth, differentiation, and oncogenic transformation. However, the final physiological effectors of p21ras-mediated signal transduction remain to be determined. We have used patch clamp electrophysiology, pharmacological agents, and transfection with specific Ras or Raf plasmids, to demonstrate that induction of a unique Ca(2+)-activated K+ channel in murine fibroblast cell lines depends on p21ras and its immediate downstream target, the Raf kinase. The importance of this channel in mitogenic signaling is further indicated by its induction in nontransformed cells by epidermal growth factor and platelet-derived growth factor and the ability of K+ channel blockers to inhibit cell proliferation. We suggest that this Ca(2+)-activated K+ channel is one ultimate physiological target of p21ras-mediated signal transduction and that it may play a role in cell proliferation and ras transformation.