Mechanisms of FSH- and Amphiregulin-Induced MAP Kinase 3/1 Activation in Pig Cumulus-Oocyte Complexes During Maturation In Vitro
Language English Country Switzerland Media electronic
Document type Journal Article
Grant support
CZ.02.1.01/0.0/0.0/15_003/0000460
The Operational Programme Research, Development and Education
QJ 1510138
The National Agency for Agricultural Research
PubMed
30866587
PubMed Central
PMC6429514
DOI
10.3390/ijms20051179
PII: ijms20051179
Knihovny.cz E-resources
- Keywords
- FSH, amphiregulin, cumulus cells, epidermal growth factor receptor, mitogen-activated protein kinase 3/1, signal transduction,
- MeSH
- Transcriptional Activation MeSH
- Amphiregulin metabolism MeSH
- ErbB Receptors metabolism MeSH
- Extracellular Signal-Regulated MAP Kinases genetics MeSH
- Follicle Stimulating Hormone pharmacology MeSH
- In Vitro Oocyte Maturation Techniques MeSH
- Cells, Cultured MeSH
- Cumulus Cells cytology drug effects metabolism MeSH
- Mitogen-Activated Protein Kinase 1 genetics MeSH
- Mitogen-Activated Protein Kinase 3 genetics MeSH
- Oocytes cytology drug effects metabolism MeSH
- Swine MeSH
- Signal Transduction drug effects MeSH
- src-Family Kinases metabolism MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Amphiregulin MeSH
- ErbB Receptors MeSH
- Extracellular Signal-Regulated MAP Kinases MeSH
- Follicle Stimulating Hormone MeSH
- Mitogen-Activated Protein Kinase 1 MeSH
- Mitogen-Activated Protein Kinase 3 MeSH
- src-Family Kinases MeSH
The maturation of mammalian oocytes in vitro can be stimulated by gonadotropins (follicle-stimulating hormone, FSH) or their intrafollicular mediator, epidermal growth factor (EGF)-like peptide-amphiregulin (AREG). We have shown previously that in pig cumulus-oocyte complexes (COCs), FSH induces expression and the synthesis of AREG that binds to EGF receptor (EGFR) and activates the mitogen-activated protein kinase 3/1 (MAPK3/1) signaling pathway. However, in this study we found that FSH also caused a rapid activation of MAPK3/1 in the cumulus cells, which cannot be explained by the de novo synthesis of AREG. The rapid MAPK3/1 activation required EGFR tyrosine kinase (TK) activity, was sensitive to SRC proto-oncogene non-receptor tyrosine kinase (SRC)-family and protein kinase C (PKC) inhibitors, and was resistant to inhibitors of protein kinase A (PKA) and metalloproteinases. AREG also induced the rapid activation of MAPK3/1 in cumulus cells, but this activation was only dependent on the EGFR TK activity. We conclude that in cumulus cells, FSH induces a rapid activation of MAPK3/1 by the ligand-independent transactivation of EGFR, requiring SRC and PKC activities. This rapid activation of MAPK3/1 precedes the second mechanism participating in the generation and maintenance of active MAPK3/1-the ligand-dependent activation of EGFR depending on the synthesis of EGF-like peptides.
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