Back to Search Start Over

Use of pregnancy-associated plasma protein-A during oocyte in vitro maturation increases IGF-1 and affects the transcriptional profile of cumulus cells and embryos from Nelore cows.

Authors :
Giroto AB
Fontes PK
Franchi FF
Dos Santos PH
Razza EM
Nogueira MFG
Maioli MA
Nogueira GP
Nunes GB
Mingoti GZ
Mareco EA
Castilho ACS
Source :
Molecular reproduction and development [Mol Reprod Dev] 2019 Nov; Vol. 86 (11), pp. 1694-1704. Date of Electronic Publication: 2019 Aug 29.
Publication Year :
2019

Abstract

Insulin-like growth factor 1 (IGF-1) activity is established by the regulation of IGF binding protein activity, which blocks IGF-1 functions, whereas pregnancy-associated plasma protein-A (PAPP-A) improves IGF-1 bioavailability and facilitates binding to IGF receptors. To further extend our understanding of the effect of exogenous PAPP-A on bovine embryo production, we added this protein during in vitro maturation of cumulus-oocyte complexes (COCs); moreover, we assessed its effects on IGF-1 quantity in the maturation medium, embryonic yield and postwarming survival, blastocyst quality, and transcript abundance. Bovine COCs were matured in a serum-free medium, either with PAPP-A supplementation (100 ng/ml) or without (control). The treatment group produced higher IGF-1 concentrations in the maturation medium; however, showed no difference on cleavage, blastocysts rates, and embryonic survival 3 and 24 hr postcryopreservation. Regarding gene expression, VNN1 was upregulated, whereas AGPAT9, FASN, EGFR, HAS2, and IMPDH1 were downregulated in PAPP-A treated. PAPP-A treated, CPT2, DNMT3A, and TFAM were upregulated, whereas ATF4 and IFITM3 were downregulated. We concluded that although the addition of PAPP-A did not affect embryo yield and blastocyst survival, higher IGF-1 levels may affect embryo competence through differential expression of genes involved in lipid metabolism, oocyte competence, and mitochondrial function.<br /> (© 2019 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1098-2795
Volume :
86
Issue :
11
Database :
MEDLINE
Journal :
Molecular reproduction and development
Publication Type :
Academic Journal
Accession number :
31468638
Full Text :
https://doi.org/10.1002/mrd.23259