Signaling by the Extracellular Matrix Protein Reelin Promotes Granulosa Cell Proliferation in the Chicken Follicle*

  1. Johannes Nimpf2
  1. From the Department of Medical Biochemistry, Max F. Perutz Laboratories, Medical University of Vienna, 1030 Vienna, Austria
  1. 2 To whom correspondence should be addressed: Max F. Perutz Laboratories, Dept. of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9/2, 1030 Vienna, Austria. Tel.: 43-1-4277-61808; Fax: 43-1-4277-9618; E-mail: Johannes.Nimpf{at}meduniwien.ac.at.
  • 1 Present address: Austrian Institute of Technology, Dept. of Health and Environment, Bioresources, Konrad Lorenz Str. 24, 3430 Tulln, Austria.

Background: The control of rapid proliferation of granulosa cells during chicken oocyte growth is unknown.

Results: Reelin is expressed in theca cells and triggers disabled-1 phosphorylation in granulosa cells via ApoER2 and the VLDL receptor.

Conclusion: The Reelin signaling pathway stimulates granulosa cell proliferation during folliculogenesis.

Significance: This work demonstrates a novel function of Reelin.

Abstract

Chicken oocytes develop in follicles and reach an enormous size because of a massive uptake of yolk precursors such as very low density lipoprotein and vitellogenin. Oocyte growth is supported by theca cells and granulosa cells, which establish dynamic and highly organized cell layers surrounding the oocyte. The signaling processes orchestrating the development of these layered structures are largely unknown. Here we demonstrate that the Reelin pathway, which determines the development of layered neuronal structures in the brain, is also active in chicken follicles. Reelin, which is expressed in theca cells, triggers a signal in granulosa cells via apolipoprotein E receptor 2 and the very low density lipoprotein receptor, resulting in the phosphorylation of disabled-1 and consecutive activation of the phosphatidylinositol 3-kinase/Akt pathway. This signaling pathway supports the proliferation of differentiated granulosa cells to keep up with the demand of cells to cover the rapidly increasing surface of the giant germ cell.

Footnotes

  • * This work was supported by Austrian Science Fund (FWF) Grant P 24767-B21 (to J. N.).

  • Received November 7, 2013.
  • Revision received February 25, 2014.
Table of Contents

This Article

  1. The Journal of Biological Chemistry 289, 10182-10191.
  1. All Versions of this Article:
    1. M113.533489v1
    2. 289/14/10182 (most recent)

Article Usage Stats

Submit your work to JBC.

You'll be in good company.