Growth/differentiation factor-15 is an abundant cytokine in human seminal plasma
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20884666
DOI
10.1093/humrep/deq264
PII: deq264
Knihovny.cz E-resources
- MeSH
- Semen Analysis MeSH
- Apoptosis drug effects MeSH
- CD4-Positive T-Lymphocytes metabolism MeSH
- Adult MeSH
- Epithelial Cells metabolism MeSH
- Forkhead Transcription Factors biosynthesis MeSH
- Leukocytes, Mononuclear drug effects MeSH
- Middle Aged MeSH
- Humans MeSH
- Cell Proliferation drug effects MeSH
- Interleukin-2 Receptor alpha Subunit metabolism MeSH
- Growth Differentiation Factor 15 physiology MeSH
- Semen metabolism MeSH
- Spermatozoa MeSH
- Cell Survival drug effects MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Forkhead Transcription Factors MeSH
- FOXP3 protein, human MeSH Browser
- IL2RA protein, human MeSH Browser
- Interleukin-2 Receptor alpha Subunit MeSH
- Growth Differentiation Factor 15 MeSH
BACKGROUND: Transforming growth factor-β cytokines have various biological effects in female reproductive tissue, including modulation of inflammatory response and induction of immune tolerance to seminal antigens in the reproductive tract. However, no studies have analyzed the presence of growth/differentiation factor-15 (GDF-15/macrophage inhibitory cytokine-1) in seminal fluid or demonstrated the quantity and form of GDF-15, its possible role or the relationship between its concentration and semen quality. METHODS: The form and the concentration of GDF-15 were determined in 53 seminal plasma samples of both fertile and infertile men by ELISA and western blot. The sperm cells of three volunteers were treated with recombinant GDF-15, and cell viability and apoptosis were assessed by flow cytometry. The effect of GDF-15 on vaginal epithelial cells and peripheral blood mononuclear cells (PBMCs) was analyzed by quantitative RT-PCR. RESULTS: The GDF-15 concentration in seminal plasma ranged from 0.2 to 6.6 μg/ml as determined by ELISA. Western blot analysis revealed that GDF-15 is present in the active form. In vitro cultivation of sperm cells with GDF-15 did not affect their viability or rates of apoptosis; however, it did inhibit proliferation of PBMCs and induce expression of FOXP3 in CD4+CD25+ cells. CONCLUSIONS: To the best of our knowledge, this is the first demonstration that GDF-15 is an abundant cytokine in seminal plasma, although its concentration is not associated with semen quality or the fertility/infertility status of the donors. Moreover, our data show that GDF-15 displays immunosuppressive characteristics.
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