The time-course of cyclic AMP signaling is critical for leukemia U-937 cell differentiation

Biochem Biophys Res Commun. 2004 Feb 13;314(3):798-804. doi: 10.1016/j.bbrc.2003.12.166.

Abstract

The regulation of the cAMP signaling is intimately involved in several cellular processes, including cell differentiation. Here, we provide strong evidence supporting that the time-course of cAMP signal is critical for leukemia U-937 cell differentiation. Three stimulating-cAMP agents were used to analyze the correlation between cAMP time-course and cell differentiation. All three agents denoted similar cAMP maximal responses in dose-response experiments. The kinetic of desensitization showed differential characteristics, while H2 receptor desensitized homologously without affecting PGE2 or forskolin effect, PGE2 response showed mixed desensitization characterized by a homologous initial phase followed by a heterologous phase. Regarding forskolin, long-term stimuli attenuated PGE2 and H2 agonist response without affecting adenylyl cyclase activity. In the absence of phosphodiesterase inhibitors, the three agents induced similar maximal cAMP levels after 5 min, but only that induced by the H2 agonist returned to basal levels. Consistent with this observation, H2 agonist was not able to induce U-937 cell maturation in contrast to PGE2 and forskolin, supporting the importance of time-course signaling in the determination of cell behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / analysis
  • Calcium / metabolism
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Division / drug effects
  • Colforsin / pharmacology
  • Complement C5a / genetics
  • Complement C5a / pharmacology
  • Cyclic AMP / physiology*
  • Dinoprostone / pharmacology
  • Dose-Response Relationship, Drug
  • Humans
  • Proto-Oncogene Proteins c-fos / analysis
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Proto-Oncogene Proteins c-myc / analysis
  • Proto-Oncogene Proteins c-myc / biosynthesis
  • Receptors, Histamine H2 / drug effects
  • Receptors, Prostaglandin E / drug effects
  • Recombinant Proteins / pharmacology
  • Signal Transduction / physiology
  • Thiazoles / pharmacology
  • Time Factors
  • U937 Cells

Substances

  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-myc
  • Receptors, Histamine H2
  • Receptors, Prostaglandin E
  • Recombinant Proteins
  • Thiazoles
  • amthamine
  • Colforsin
  • Complement C5a
  • Cyclic AMP
  • Dinoprostone
  • Calcium