Interleukin-6-induced tyrosine phosphorylation of phospholipase C-gamma1 in PC12 cells

Mol Cells. 2000 Aug 31;10(4):469-74.

Abstract

Phospholipase C (PLC)-gamma1 plays a pivotal role in the signal transduction pathway mediated by growth factors. In this study, we found that neurite outgrowth of pheochromocytoma (PC12) cells was significantly induced by interleukin-6 (IL-6). Stimulation of PC12 cells with IL-6 led to tyrosine phosphorylation of PLC-gamma1 in a dose- and time-dependent manner. IL-6 stimulation also increased the hydrolysis of phosphatidylinositol 4,5-bisphosphate. Accumulation of total inositol phosphate as well as tyrosine phosphorylation of PLC-gamma1 was inhibited by the pretreatment of protein kinase inhibitors such as genistein and staurosporine. These results suggest that PLC-gamma1 may be involved in the signal transduction pathway of IL-6-induced PC12 cell differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Genistein / pharmacology
  • Inositol Phosphates / metabolism
  • Interleukin-6 / pharmacology*
  • Isoenzymes / metabolism
  • Isoenzymes / physiology*
  • Neurites / drug effects
  • Neurites / metabolism
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism*
  • PC12 Cells
  • Phospholipase C gamma
  • Phosphorylation
  • Phosphotyrosine / drug effects
  • Phosphotyrosine / metabolism*
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Rats
  • Signal Transduction
  • Type C Phospholipases / metabolism
  • Type C Phospholipases / physiology*

Substances

  • Inositol Phosphates
  • Interleukin-6
  • Isoenzymes
  • Phosphotyrosine
  • Genistein
  • Protein-Tyrosine Kinases
  • Type C Phospholipases
  • Phospholipase C gamma