Induction of chemokines and prostaglandin synthesis pathways in luteinized human granulosa cells: potential role of luteotropin withdrawal and prostaglandin F2α in regression of the human corpus luteum

Reprod Biol. 2015 Dec;15(4):247-56. doi: 10.1016/j.repbio.2015.10.003. Epub 2015 Oct 24.

Abstract

Our objective was to determine the effects of prostaglandin F2α (PGF2α) and withdrawal of luteotropic stimulants (forskolin or hCG) on expression of chemokines and prostaglandin-endoperoxide synthase 2 (PTGS2) in luteinized human granulosa cells. Human granulosa cells were collected from 12 women undergoing oocyte retrieval and were luteinized in vitro with forskolin or hCG. In first experiment, granulosa-lutein cells were treated with PGF2α, the primary luteolytic hormone in most species. In second experiment, granulosa cells that had been luteinized for 8 d had luteotropins withdrawn for 1, 2, or 3 d. Treatment with PGF2α induced mRNA for chemokine (c-x-c motif) ligand 2 (CXCL2) and CXC ligand 8 (CXCL8; also known as interleukin-8) in granulosa cells luteinized for 8 d but not in cells that were only luteinized for 2 d. Similarly, luteinization of human granulosa cells for 8 d with forskolin or hCG followed by withdrawal of luteotropic stimulants, not only decreased P4 production, but also increased mRNA concentrations for CXCL8, CXCL-2 (after forskolin withdrawal), and PTGS2. These results provide evidence for two key steps in differentiation of luteolytic capability in human granulosa cells. During 8 d of luteinization, granulosa cells acquire the ability to respond to luteolytic factors, such as PGF2α, with induction of genes involved in immune function and PG synthesis. Finally, a decline in luteotropic stimuli triggers similar pathways leading to induction of PTGS2 and possibly intraluteal PGF2α production, chemokine expression, leukocyte infiltration and activation, and ultimately luteal regression.

Keywords: Chemokines; Luteinized granulosa cells; Luteolysis; PGF(2α); PTGS2.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cells, Cultured
  • Chemokine CXCL2 / genetics
  • Chemokine CXCL2 / metabolism
  • Chemokines / biosynthesis*
  • Chorionic Gonadotropin / pharmacology
  • Colforsin / pharmacology
  • Corpus Luteum / physiology*
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Dinoprost / biosynthesis*
  • Female
  • Gene Expression Regulation / physiology
  • Humans
  • Interleukin-8 / genetics
  • Interleukin-8 / metabolism
  • Luteolysis / physiology*
  • Pituitary Hormones, Anterior / genetics
  • Pituitary Hormones, Anterior / metabolism*
  • Progesterone / metabolism
  • Prostaglandins / biosynthesis*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • CXCL2 protein, human
  • CXCL8 protein, human
  • Chemokine CXCL2
  • Chemokines
  • Chorionic Gonadotropin
  • Interleukin-8
  • Pituitary Hormones, Anterior
  • Prostaglandins
  • RNA, Messenger
  • Colforsin
  • Progesterone
  • luteotropin, decidual
  • Dinoprost
  • Cyclooxygenase 2
  • PTGS2 protein, human