Spatial distribution and receptor specificity of zebrafish Kit system--evidence for a Kit-mediated bi-directional communication system in the preovulatory ovarian follicle

PLoS One. 2013;8(2):e56192. doi: 10.1371/journal.pone.0056192. Epub 2013 Feb 8.

Abstract

Consisting of Kit ligand and receptor Kit, the Kit system is involved in regulating many ovarian functions such as follicle activation, granulosa cell proliferation, and oocyte growth and maturation. In mammals, Kit ligand is derived from the granulosa cells and Kit receptor is expressed in the oocyte and theca cells. In the zebrafish, the Kit system contains two ligands (Kitlga and Kitlgb) and two receptors (Kita and Kitb). Interestingly, Kitlga and Kitb are localized in the somatic follicle cells, but Kitlgb and Kita are expressed in the oocyte. Using recombinant zebrafish Kitlga and Kitlgb, we demonstrated that Kitlga preferentially activated Kita whereas Kitlgb specifically activated Kitb by Western analysis for receptor phosphorylation. In support of this, Kitlgb triggered a stronger and longer MAPK phosphorylation in follicle cells than Kitlga, whereas Kitlga but not Kitlgb activated MAPK in the denuded oocytes, in agreement with the distribution of Kita and Kitb in the follicle and their specificity for Kitlga and Kitlgb. Further analysis of the interaction between Kit ligands and receptors by homology modeling showed that Kitlga-Kita and Kitlgb-Kitb both have more stable electrostatic interaction than Kitlgb-Kita or Kitlga-Kitb. A functional study of Kit involvement in final oocyte maturation showed that Kitlga and Kitlgb both suppressed the spontaneous maturation significantly; in contrast, Kitlgb but not Kitlga significantly promoted 17α, 20β-dihydroxy-4-pregnen-3-one (DHP) -induced oocyte maturation. Our results provided strong evidence for a Kit-mediated bi-directional communication system in the zebrafish ovarian follicle, which could be part of the complex interplay between the oocyte and the follicle cells in the development of follicles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • COS Cells
  • Cell Communication*
  • Chlorocebus aethiops
  • Cricetinae
  • Cricetulus
  • Enzyme Activation
  • Female
  • Male
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism
  • Oocytes / cytology
  • Oocytes / metabolism
  • Ovarian Follicle / cytology*
  • Ovarian Follicle / metabolism
  • Ovarian Follicle / physiology*
  • Ovulation*
  • Phosphorylation
  • Protein Transport
  • Proto-Oncogene Proteins c-kit / metabolism*
  • Species Specificity
  • Stem Cell Factor / metabolism*
  • Substrate Specificity
  • Zebrafish Proteins / metabolism
  • Zebrafish*

Substances

  • Stem Cell Factor
  • Zebrafish Proteins
  • Proto-Oncogene Proteins c-kit
  • Mitogen-Activated Protein Kinases

Grants and funding

The work was substantially supported by grants from the Research Grants Council (CUHK464707, 464308 and 464409) and the Areas of Excellence (AoE) Scheme on Marine Environmental Research and Innovative Technology (MERIT) of the Hong Kong Special Administrative Region to W. Ge. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.