Alpha 2-adrenergic stimulation promotes preadipocyte proliferation. Involvement of mitogen-activated protein kinases

J Biol Chem. 1994 Dec 2;269(48):30254-9.

Abstract

Primary cultures of rat preadipocytes were shown to express alpha 2- and beta-adrenoreceptors when maintained in serum-deprived medium. alpha 2-Adrenoreceptor stimulation led to an increase in cell number, whereas beta-adrenoreceptor stimulation was without effect. On 3T3-F442A clones stably transfected with the human alpha 2-C10 gene and expressing a physiologically related number of alpha 2-adrenoreceptors to overexpression, the proliferative effect of alpha 2-adrenoreceptor agonist UK14304 was proportional to the level of alpha 2-adrenoreceptor expressed in individual clones and required alpha-2 adrenoreceptor stimulation. Analysis of the signaling pathway linked to alpha 2-adrenoreceptor activation showed that the mitogenic effect was adenylyl cyclase- and protein kinase C-independent. It was pertussis toxin-sensitive, implying the involvement of pertussis toxin-sensitive G proteins. The activation of the mitogen-activated protein kinase pathway was increased after alpha 2-adrenoreceptor stimulation in both 3T3-F442 clones and rat preadipocytes and inhibited by pertussis toxin treatment. So, catecholamines are involved in the control of white preadipocyte proliferation through the alpha 2-adrenoreceptor activation, linked to the mitogen-activated protein kinase pathway.

MeSH terms

  • 3T3 Cells
  • Adenylate Cyclase Toxin
  • Adenylyl Cyclases / metabolism
  • Adipocytes / cytology*
  • Adipocytes / drug effects
  • Adipose Tissue / cytology
  • Adipose Tissue / drug effects
  • Adipose Tissue / physiology*
  • Adrenergic alpha-Agonists / pharmacology*
  • Adrenergic alpha-Antagonists / metabolism
  • Animals
  • Brimonidine Tartrate
  • Bucladesine / pharmacology
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
  • Cell Division / drug effects
  • Cells, Cultured
  • Clone Cells
  • Clonidine / pharmacology*
  • Cyclic AMP / metabolism
  • Dioxanes / metabolism
  • Humans
  • Idazoxan / analogs & derivatives
  • Kinetics
  • Male
  • Mice
  • Pertussis Toxin
  • Quinolizines / metabolism
  • Quinoxalines / pharmacology*
  • Rats
  • Rats, Wistar
  • Receptors, Adrenergic, alpha-2 / drug effects
  • Receptors, Adrenergic, alpha-2 / metabolism
  • Receptors, Adrenergic, alpha-2 / physiology*
  • Recombinant Proteins / drug effects
  • Recombinant Proteins / metabolism
  • Transfection
  • Virulence Factors, Bordetella / pharmacology

Substances

  • Adenylate Cyclase Toxin
  • Adrenergic alpha-Agonists
  • Adrenergic alpha-Antagonists
  • Dioxanes
  • Quinolizines
  • Quinoxalines
  • Receptors, Adrenergic, alpha-2
  • Recombinant Proteins
  • Virulence Factors, Bordetella
  • L 657743
  • Brimonidine Tartrate
  • Bucladesine
  • Cyclic AMP
  • 2-methoxyidazoxan
  • Pertussis Toxin
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Adenylyl Cyclases
  • Clonidine
  • Idazoxan