Email updates

Keep up to date with the latest news and content from BMC Genomics and BioMed Central.

Open Access Highly Accessed Research article

Gene expression profiling of rat spermatogonia and Sertoli cells reveals signaling pathways from stem cells to niche and testicular cancer cells to surrounding stroma

Stephan Ryser16, Dominique Glauser2, Michelle Vigier3, Yong Qiang Zhang1, Philippe Tachini4, Werner Schlegel2, Philippe Durand35 and Irmgard Irminger-Finger1*

Author Affiliations

1 Molecular Gynecology and Obstetrics Laboratory, Geneva University Hospitals, Geneva, Switzerland

2 Fondation pour Recherches Médicales, Geneva, Switzerland

3 INSERM, UMR 418; INRA, UMR 1245, Debrousse Hospital, Lyon, France

4 EDEL Therapeutics, Lausanne, Switzerland

5 Institut de Génomique Fonctionnelle de Lyon, Université de Lyon; Université Lyon 1; CNRS; INRA; Ecole Normale Supérieure de Lyon, Lyon, France

6 Lausanne University Hospital, Lausanne, Switzerland

For all author emails, please log on.

BMC Genomics 2011, 12:29  doi:10.1186/1471-2164-12-29

Published: 13 January 2011

Abstract

Background

Stem cells and their niches are studied in many systems, but mammalian germ stem cells (GSC) and their niches are still poorly understood. In rat testis, spermatogonia and undifferentiated Sertoli cells proliferate before puberty, but at puberty most spermatogonia enter spermatogenesis, and Sertoli cells differentiate to support this program. Thus, pre-pubertal spermatogonia might possess GSC potential and pre-pubertal Sertoli cells niche functions. We hypothesized that the different stem cell pools at pre-puberty and maturity provide a model for the identification of stem cell and niche-specific genes. We compared the transcript profiles of spermatogonia and Sertoli cells from pre-pubertal and pubertal rats and examined how these related to genes expressed in testicular cancers, which might originate from inappropriate communication between GSCs and Sertoli cells.

Results

The pre-pubertal spermatogonia-specific gene set comprised known stem cell and spermatogonial stem cell (SSC) markers. Similarly, the pre-pubertal Sertoli cell-specific gene set comprised known niche gene transcripts. A large fraction of these specifically enriched transcripts encoded trans-membrane, extra-cellular, and secreted proteins highlighting stem cell to niche communication. Comparing selective gene sets established in this study with published gene expression data of testicular cancers and their stroma, we identified sets expressed genes shared between testicular tumors and pre-pubertal spermatogonia, and tumor stroma and pre-pubertal Sertoli cells with statistic significance.

Conclusions

Our data suggest that SSC and their niche specifically express complementary factors for cell communication and that the same factors might be implicated in the communication between tumor cells and their micro-enviroment in testicular cancer.