Progesterone-regulated cyclic modulation of membrane metalloendopeptidase (enkephalinase) in human endometrium

J Biol Chem. 1991 Dec 5;266(34):23041-7.

Abstract

Membrane metalloendopeptidase (MMEP; EC 3.4.24.11; enkephalinase) catalyzes the degradation of endothelins, enkephalins, atrial natriuretic factor, substance P, and other small bioactive peptides. We found that MMEP is present in human endometrium, localized primarily in stromal cells of this tissue, and that the specific activity of MMEP (and immunoreactive MMEP protein) in endometrial tissue is correlated in a highly significant positive manner with the concentration of progesterone in plasma. In estrogen-treated, human endometrial stromal cells in monolayer culture, the specific activity of MMEP increases in response to treatment with progestin; and, this increase is accompanied by increases in immunoreactive MMEP protein, newly synthesized MMEP, and MMEP mRNA.

Publication types

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

MeSH terms

  • Adult
  • Blotting, Northern
  • Cell Membrane / enzymology
  • Cells, Cultured
  • Endometrium / cytology
  • Endometrium / enzymology*
  • Endometrium / ultrastructure
  • Female
  • Humans
  • Immunoblotting
  • Kinetics
  • Menstrual Cycle
  • Metalloendopeptidases / genetics
  • Metalloendopeptidases / metabolism*
  • Organ Specificity
  • Pregnancy
  • Progesterone / blood
  • Progesterone / physiology*
  • RNA, Messenger / metabolism

Substances

  • RNA, Messenger
  • Progesterone
  • Metalloendopeptidases