A negative feedback system between oocyte bone morphogenetic protein 15 and granulosa cell kit ligand: its role in regulating granulosa cell mitosis

Proc Natl Acad Sci U S A. 2002 Jun 11;99(12):8060-5. doi: 10.1073/pnas.122066899. Epub 2002 Jun 4.

Abstract

Although the existence of a regulatory paracrine feedback system between oocytes and follicular somatic cells has been postulated for some time, there has not yet been any definitive evidence that such a communication system exists. Herein we present a previously undescribed oocyte-granulosa cell (GC) feedback communication system involving an oocyte-derived factor, bone morphogenetic protein-15 (BMP-15) and a GC-derived factor, kit ligand (KL), both of which have been shown to be crucial regulators of female reproduction. We used a coculture system of rat oocytes and GCs and found that BMP-15 stimulates KL expression in GCs, whereas KL inhibits BMP-15 expression in oocytes, thus forming a negative feedback loop. Moreover, KL, like BMP-15, exhibited mitotic activity on GCs in the presence of oocytes. Because c-kit (KL receptor) is expressed in oocytes but not GCs, the oocytes must be involved in mediating the KL-induced GC mitosis. Furthermore, the blockage of c-kit signaling in oocytes by using a c-kit neutralizing antibody markedly suppressed BMP-15-induced GC mitosis, suggesting that the oocyte must play a role in the GC responses to BMP-15. In contrast, the c-kit antibody had no effect on the mitotic activities of two other known GC mitogens, activin-A and BMP-7. Altogether, this study presents direct evidence of a negative feedback system governed by oocyte-derived BMP-15 and GC-derived KL, and demonstrates that the mitotic activities of BMP-15 and KL for GCs depend on this oocyte-GC communication system. We hypothesize that the negative feedback system most likely plays a pivotal role in early folliculogenesis.

Publication types

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

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 15
  • Bone Morphogenetic Proteins / physiology
  • DNA Replication / drug effects
  • Diethylstilbestrol / pharmacology
  • Feedback
  • Female
  • Granulosa Cells / cytology*
  • Granulosa Cells / drug effects
  • Granulosa Cells / physiology
  • Growth Differentiation Factor 9
  • Growth Substances / genetics
  • Growth Substances / physiology*
  • Intercellular Signaling Peptides and Proteins*
  • Mitosis / drug effects
  • Mitosis / physiology*
  • Models, Biological
  • Oocytes / cytology
  • Oocytes / drug effects
  • Oocytes / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cell Factor / genetics
  • Stem Cell Factor / physiology*

Substances

  • Bmp15 protein, rat
  • Bone Morphogenetic Protein 15
  • Bone Morphogenetic Proteins
  • Gdf9 protein, rat
  • Growth Differentiation Factor 9
  • Growth Substances
  • Intercellular Signaling Peptides and Proteins
  • Stem Cell Factor
  • Diethylstilbestrol