SOCS genes expression during physiological and perturbed implantation in bovine endometrium.

Reproduction

INRAUMR1198 Biologie du Développement et Reproduction, F-78350 Jouy-en-Josas, FranceSchool of Agriculture and Food ScienceUniversity College Dublin, Dublin, IrelandCentre for Reproductive ImmunologyInstitute of Life Science, College of Medicine, Swansea University, Swansea SA28PP, UKDepartment of Pathology and ImmunologyBaylor College of Medicine, Houston, Texas, USASchool of Veterinary Medicine and ScienceUniversity of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, Leicestershire, UK

Published: December 2014

In mammals, suppressor of cytokine signalling (CISH, SOCS1 to SOCS7) factors control signalling pathways involved in the regulation of numerous physiological processes including pregnancy. In order to gain new insights into the biological functions of SOCS in the endometrium, a comprehensive analysis of SOCS gene expression was carried out in bovine caruncular (CAR) and intercaruncular (ICAR) tissues collected i) during the oestrous cycle, ii) at the time of maternal recognition of pregnancy and at implantation in inseminated females, iii) following uterine interferon-tau (IFNT) infusion at day 14 post-oestrus, iv) following a period of controlled intravaginal progesterone release and v) following transfer of embryos by somatic-cell nuclear transfer (SCNT). The regulatory effects of IFNT on in vitro cultured epithelial and stromal cells were also examined. Altogether, our data showed that CISH, SOCS4, SOCS5 and SOCS7 mRNA levels were poorly affected during luteolysis and pregnancy. In contrast, SOCS1, SOCS2, SOCS3 and SOCS6 mRNA levels were strongly up-regulated at implantation (day 20 of pregnancy). Experimental in vitro and in vivo models demonstrated that only CISH, SOCS1, SOCS2 and SOCS3 were IFNT-induced genes. Immunohistochemistry showed an intense SOCS3 and SOCS6 staining in the nucleus of luminal and glandular epithelium and of stromal cells of pregnant endometrium. Finally, SOCS3 expression was significantly increased in SCNT pregnancies in keeping with the altered immune function previously reported in this model of compromised implantation. Collectively, our data suggest that spatio-temporal changes in endometrial SOCS gene expression reflect the acquisition of receptivity, maternal recognition of pregnancy and implantation.

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Source
http://dx.doi.org/10.1530/REP-14-0214DOI Listing

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