alpha 1-Adrenergic receptor subtypes differentially control the cell cycle of transfected CHO cells through a cAMP-dependent mechanism involving p27Kip1

J Biol Chem. 2003 Jan 3;278(1):672-8. doi: 10.1074/jbc.M201375200. Epub 2002 Oct 29.

Abstract

Three distinct subtypes of alpha(1)-adrenergic receptors (alpha(1)A-, alpha(1)B-, and alpha(1)D-AR) play a prominent role in cell growth. However, little is known about subtype-specific effects on cell proliferation. The activation of alpha(1)A- or alpha(1)B-AR inhibits serum-promoted cell proliferation, whereas alpha(1)D-AR activation does not show such an inhibitory effect. Notably, cell-cycle progression was blocked at G(1)/S transition after activation of alpha(1)A/alpha(1)B-AR but not of alpha(1)D-AR. In agreement with the differential cell proliferation effect, cAMP production was increased after activation of alpha(1)A/alpha(1)B-AR but not alpha(1)D-AR, whereas all alpha(1)-AR subtypes are associated with inositol 1,4,5-trisphosphate production and mitogen-activated protein kinase activation in a similar fashion. Furthermore, the serum-induced reduction in the levels of the cyclin-dependent kinase inhibitor, p27(Kip1), was blocked after activation of alpha(1)A/alpha(1)B-AR but not alpha(1)D-AR. These results show that alpha(1)-AR subtypes differentially activate the cAMP/p27(Kip1) pathway and thereby have differential inhibitory effects on cell proliferation. Subtype-dependent effects should be taken into consideration when assessing the physiological response of native cells where alpha(1)-AR subtypes are generally co-expressed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cell Cycle / physiology*
  • Cell Cycle Proteins / metabolism*
  • Cricetinae
  • Culture Media
  • Cyclic AMP / metabolism*
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases / antagonists & inhibitors
  • Flow Cytometry
  • Humans
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism*
  • Receptors, Adrenergic, alpha-1 / genetics
  • Receptors, Adrenergic, alpha-1 / metabolism*
  • Signal Transduction / physiology
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Cell Cycle Proteins
  • Culture Media
  • Protein Isoforms
  • Receptors, Adrenergic, alpha-1
  • Tumor Suppressor Proteins
  • Cyclin-Dependent Kinase Inhibitor p27
  • Inositol 1,4,5-Trisphosphate
  • Cyclic AMP
  • Cyclin-Dependent Kinases
  • Mitogen-Activated Protein Kinases