Expression of the chicken GDNF family receptor α-1 as a marker of spermatogonial stem cells
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24060137
DOI
10.1016/j.anireprosci.2013.08.006
PII: S0378-4320(13)00236-4
Knihovny.cz E-resources
- Keywords
- Chicken spermatogonial stem cell, GFRα1, Male germ line transplantation,
- MeSH
- Biomarkers MeSH
- Adult Stem Cells physiology MeSH
- Genotype MeSH
- Cloning, Molecular MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Molecular Sequence Data MeSH
- Antibodies blood MeSH
- Glial Cell Line-Derived Neurotrophic Factor Receptors genetics metabolism MeSH
- Gene Expression Regulation physiology MeSH
- Amino Acid Sequence MeSH
- Testis cytology MeSH
- Stem Cell Transplantation veterinary MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- Antibodies MeSH
- Glial Cell Line-Derived Neurotrophic Factor Receptors MeSH
The identification, enrichment and subsequent isolation of spermatogonial stem cells (SSCs) are integral to the success of SCC transplants between fertile donor and sterilized recipient males. In birds generally and particularly in chicken, SSC-specific has yet to be identified. The receptor for glial cell-derived neurotrophic factor (GDNF), i.e. GDNF family receptor alpha-1 (GFRα1), has been identified as a potential marker for different mouse spermatogonial subtypes. In the present study, we characterized the chicken cGFRα1 receptor and compared its predicted amino-acid sequence with mouse, rat and human GFRα1 proteins. Using specific polyclonal mouse anti-cGFRα1 serum, a total of 2.8% cells were recognized as cGFRα1-positive among isolated testicular cells recovered from sexually mature cockerels. The percentages of cGFRα1-positive testicular cells with haploid, diploid, tetraploid and SP DNA content were 1.6%, 2.5%, 39.3% and 76.8%, respectively. The presence of cGFRα1 protein on the surfaces of all cells of the seminiferous epithelium was confirmed by immunocytochemical and immunohistochemical analyses. Tissue specificity of cGFRα1 mRNA expression was significantly higher in adult testes compared to brain tissue which itself was several times higher than tissues prepared from the spleen, liver and heart. No expression was observed in muscular tissue. At last, we demonstrated the successful repopulation of sterilized recipient's testes with transplanted cGFRα1-positive donor testicular cells. Recipient males subsequently produced functional heterologous spermatozoa capable of fertilizing an ovum and obtaining chicks with donor cell genotypes.
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