Requirement of phospholipase C-catalyzed hydrolysis of phosphatidylcholine for maturation of Xenopus laevis oocytes in response to insulin and ras p21

J Biol Chem. 1991 Apr 15;266(11):6825-9.

Abstract

Recent studies have demonstrated the activation of phospholipase C-mediated hydrolysis of phosphatidylcholine both by growth factors and by the product of ras oncogene, ras p21. Also, evidence has been presented indicating that the stimulation of this phospholipid-degradative pathway is sufficient to activate mitogenesis in fibroblasts. In Xenopus laevis oocytes, microinjection of transforming ras p21 is a potent inducer of maturation, whereas microinjection of a neutralizing anti-ras p21 antibody specifically inhibits maturation induced by insulin but not by progesterone. The results presented here demonstrated that microinjection of phosphatidylcholine-hydrolyzing phospholipase C is sufficient to induce maturation of Xenopus laevis oocytes. Furthermore, microinjection of a neutralizing anti-phosphatidylcholine-hydrolyzing phospholipase C specifically blocks the maturation program induced by ras p21/insulin but not by progesterone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diglycerides / metabolism
  • Female
  • Genes, ras*
  • Hydrolysis
  • Insulin / pharmacology*
  • Kinetics
  • Oocytes / drug effects
  • Oocytes / physiology*
  • Phosphatidic Acids / metabolism
  • Phosphatidylcholines / metabolism*
  • Progesterone / pharmacology
  • Propranolol / pharmacology
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Proto-Oncogene Proteins p21(ras) / physiology*
  • Type C Phospholipases / metabolism*
  • Xenopus laevis

Substances

  • Diglycerides
  • Insulin
  • Phosphatidic Acids
  • Phosphatidylcholines
  • Progesterone
  • Propranolol
  • Type C Phospholipases
  • Proto-Oncogene Proteins p21(ras)