Rapamycin-FKBP12 blocks proliferation, induces differentiation, and inhibits cdc2 kinase activity in a myogenic cell line

J Biol Chem. 1993 Dec 5;268(34):25385-8.

Abstract

Rapamycin is a potent immunosuppressant that binds to the cytosolic protein, FKBP12, and blocks T cell activation. Here we report that rapamycin also blocks myogenic proliferation and induces differentiation, associated with a decrease in p34cdc2 activity and cyclin A levels. In yeast and mammals, rapamycin blocks cell cycle progression by causing G1 arrest, arguing for a conserved signaling pathway governing the G1 to S transition. p34cdc2 has been shown to play a role in both the transition from G1 to S and from G2 to M in yeast. In higher eukaryotes the role of p34cdc2 in G1 to S transition is less clear. Rapamycin and the structurally related macrolide antibiotic FK506 both bind to a cytosolic protein, the FK506-binding protein (FKBP12). We show that inhibition of myogenic proliferation is achieved at low doses of rapamycin (< 1 ng/ml) and is competed by a molar excess of FK506, indicating specificity for FKBP12. The distinct FK506-calcineurin pathway did not affect myogenic proliferation, differentiation, or p34cdc2 kinase activity. Thus, the rapamycin-FKBP12 signaling pathway involves a specific and direct effect on p34cdc2 kinase activity at the G1 to S transition and identifies a regulatory step during myogenic differentiation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • CDC2 Protein Kinase / antagonists & inhibitors*
  • Carrier Proteins / metabolism*
  • Cell Cycle / drug effects
  • Cell Differentiation / drug effects
  • Cell Division / drug effects
  • Cell Line
  • Cyclins / antagonists & inhibitors
  • Cyclins / biosynthesis
  • Heat-Shock Proteins / metabolism*
  • Immunosuppressive Agents / pharmacology*
  • Kinetics
  • Mice
  • Muscles / cytology*
  • Muscles / drug effects
  • Muscles / enzymology
  • Polyenes / metabolism
  • Polyenes / pharmacology*
  • Sirolimus
  • Tacrolimus / metabolism
  • Tacrolimus Binding Proteins

Substances

  • Carrier Proteins
  • Cyclins
  • Heat-Shock Proteins
  • Immunosuppressive Agents
  • Polyenes
  • CDC2 Protein Kinase
  • Tacrolimus Binding Proteins
  • Sirolimus
  • Tacrolimus