Obliteration of alpha-melanocyte-stimulating hormone derived from POMC in pituitary and brains of PC2-deficient mice

J Neurochem. 2003 Aug;86(3):556-63. doi: 10.1046/j.1471-4159.2003.01856.x.

Abstract

Alpha-melanocyte-stimulating hormone (alpha-MSH) is a neuropeptide expressed in pituitary and brain that is known to regulate energy balance, appetite control, and neuroimmune functions. The biosynthesis of alpha-MSH requires proteolytic processing of the proopiomelanocortin (POMC) precursor. Therefore, this study investigated the in vivo role of the prohormone convertase 2 (PC2) processing enzyme for production of alpha-MSH in PC2-deficient mice. Specific detection of alpha-MSH utilized radioimmunoassay (RIA) that does not crossreact with the POMC precursor, and which does not crossreact with other adrenocorticotropin hormone (ACTH) and beta-endorphin peptide products derived from POMC. alpha-MSH in PC2-deficient mice was essentially obliterated in pituitary, hypothalamus, cortex, and other brain regions (collectively), compared to wild-type controls. These results demonstrate the critical requirement of PC2 for the production of alpha-MSH. The absence of alpha-MSH was accompanied by accumulation of ACTH, ACTH-containing imtermediates, and POMC precursor. ACTH was increased in pituitary and hypothalamus of PC2-deficient mice, evaluated by RIA and reversed-phase high pressure liquid chromatography (RP-HPLC). Accumulation of ACTH demonstrates its role as a PC2 substrate that can be converted for alpha-MSH production. Further analyses of POMC-derived intermediates in pituitary, conducted by denaturing western blot conditions, showed accumulation of ACTH-containing intermediates in pituitaries of PC2-deficient mice, which implicate participation of such intermediates as PC2 substrates. Moreover, accumulation of POMC was observed in PC2-deficient mice by western blots with anti-ACTH and anti-beta-endorphin. In addition, increased beta-endorphin1-31 was observed in pituitary and hypothalamus of PC2-deficient mice, suggesting beta-endorphin1-31 as a substrate for PC2 in these tissues. Overall, these studies demonstrated that the PC2 processing enzyme is critical for the in vivo production of alpha-MSH in pituitary and brain.

Publication types

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

MeSH terms

  • Adrenocorticotropic Hormone / analysis
  • Adrenocorticotropic Hormone / metabolism
  • Animals
  • Blotting, Western
  • Brain / metabolism*
  • Brain Chemistry
  • Cerebral Cortex / chemistry
  • Cerebral Cortex / metabolism
  • Hypothalamus / chemistry
  • Hypothalamus / metabolism
  • Mice
  • Mice, Knockout
  • Peptide Fragments / analysis
  • Peptide Fragments / metabolism
  • Pituitary Gland / metabolism*
  • Pro-Opiomelanocortin / analysis
  • Pro-Opiomelanocortin / metabolism*
  • Proprotein Convertase 2
  • Radioimmunoassay
  • Subtilisins / deficiency*
  • Subtilisins / genetics
  • alpha-MSH / analysis
  • alpha-MSH / deficiency*
  • beta-Endorphin / analysis
  • beta-Endorphin / metabolism

Substances

  • Peptide Fragments
  • alpha-MSH
  • beta-Endorphin
  • Pro-Opiomelanocortin
  • Adrenocorticotropic Hormone
  • Subtilisins
  • Proprotein Convertase 2