TY - JOUR
T1 - Analysis of STAT1 expression and biological activity reveals interferon-tau-dependent STAT1-regulated SOCS genes in the bovine endometrium
AU - Carvalho, A. Vitorino
AU - Eozenou, C.
AU - Healey, G. D.
AU - Forde, N.
AU - Reinaud, P.
AU - Chebrout, M.
AU - Gall, L.
AU - Rodde, N.
AU - Padilla, A. Lesage
AU - Delville, C. Giraud
AU - Leveugle, M.
AU - Richard, C.
AU - Sheldon, I. M.
AU - Lonergan, P.
AU - Jolivet, G.
AU - Sandra, O.
N1 - Funding Information:
We are grateful to M. Pannetier, S. Kennedy and his team (INRA, Jouy-enJosas, France) for the ChIP experiment support as well as V. Loux and J-F. Gibra for promoter analyses (INRA). We thank G. Charpigny (INRA) for supplying recombinant ovine IFNT. We also thank the PICT platform (INRA) for access to the Agilent analyser, the MIMA2 platform (INRA) for access to confocal microscopy and the staff of INRA experimental units (Avord, France; Saint-Genès-Champanelle, France; Nouzilly, France) for animal management and tissue collection. A. Vitorino Carvalho is a PhD recipient from the French Ministry for Teaching and Research – Doctoral School ED419 Université Paris Sud. This work was partially supported by the European Network of Excellence ''Embryo Implantation Control'' (EMBIC; LSHN-CT-2004–512040; coordinator: G. Chaouat, INSERM), ANR-08-GENM-037, AIP Bioressources CHIPSTRAFFIC, Science Foundation Ireland and the Higher Education Authority Irish Centre for High-End Computing (ICHEC) and the UK Biotechnology and Biological Sciences Research Council (BBSRC; BB/I017240/1).
Funding Information:
We are grateful to M. Pannetier, S. Kennedy and his team (INRA, Jouy-enJosas, France) for the ChIP experiment support as well as V. Loux and J-F. Gibra for promoter analyses (INRA). We thank G. Charpigny (INRA) for supplying recombinant ovine IFNT. We also thank the PICT platform (INRA) for access to the Agilent analyser, the MIMA2 platform (INRA) for access to confocal microscopy and the staff of INRA experimental units (Avord, France; Saint-Gen?s-Champanelle, France; Nouzilly, France) for animal management and tissue collection. A. Vitorino Carvalho is a PhD recipient from the French Ministry for Teaching and Research ? Doctoral School ED419 Universit? Paris Sud. This work was partially supported by the European Network of Excellence ''Embryo Implantation Control'' (EMBIC; LSHN-CT-2004?512040; coordinator: G. Chaouat, INSERM), ANR-08-GENM-037, AIP Bioressources CHIPSTRAFFIC, Science Foundation Ireland and the Higher Education Authority Irish Centre for High-End Computing (ICHEC) and the UK Biotechnology and Biological Sciences Research Council (BBSRC; BB/I017240/1).
Publisher Copyright:
© CSIRO 2016.
PY - 2016
Y1 - 2016
N2 - Signal transducer and activator of transcription (STAT) proteins are critical for the regulation of numerous biological processes. In cattle, microarray analyses identified STAT1 as a differentially expressed gene in the endometrium during the peri-implantation period. To gain new insights about STAT1 during the oestrous cycle and early pregnancy, we investigated STAT1 transcript and protein expression, as well as its biological activity in bovine tissue and cells of endometrial origin. Pregnancy increased STAT1 expression on Day 16, and protein and phosphorylation levels on Day 20. In cyclic and pregnant females, STAT1 was located in endometrial cells but not in the luminal epithelium at Day 20 of pregnancy. The expression of STAT1 during the oestrous cycle was not affected by progesterone supplementation. In vivo and in vitro, interferon-tau (IFNT) stimulated STAT1 mRNA expression, protein tyrosine phosphorylation and nuclear translocation. Using chromatin immunoprecipitation in IFNT-stimulated endometrial cells, we demonstrated an increase of STAT1 binding on interferon regulatory factor 1 (IRF1), cytokine-inducible SH2-containing protein (CISH), suppressor of cytokine signaling 1 and 3 (SOCS1, SOCS3) gene promoters consistent with the induction of their transcripts. Our data provide novel molecular insights into the biological functions of STAT1 in the various cells composing the endometrium during maternal pregnancy recognition and implantation.
AB - Signal transducer and activator of transcription (STAT) proteins are critical for the regulation of numerous biological processes. In cattle, microarray analyses identified STAT1 as a differentially expressed gene in the endometrium during the peri-implantation period. To gain new insights about STAT1 during the oestrous cycle and early pregnancy, we investigated STAT1 transcript and protein expression, as well as its biological activity in bovine tissue and cells of endometrial origin. Pregnancy increased STAT1 expression on Day 16, and protein and phosphorylation levels on Day 20. In cyclic and pregnant females, STAT1 was located in endometrial cells but not in the luminal epithelium at Day 20 of pregnancy. The expression of STAT1 during the oestrous cycle was not affected by progesterone supplementation. In vivo and in vitro, interferon-tau (IFNT) stimulated STAT1 mRNA expression, protein tyrosine phosphorylation and nuclear translocation. Using chromatin immunoprecipitation in IFNT-stimulated endometrial cells, we demonstrated an increase of STAT1 binding on interferon regulatory factor 1 (IRF1), cytokine-inducible SH2-containing protein (CISH), suppressor of cytokine signaling 1 and 3 (SOCS1, SOCS3) gene promoters consistent with the induction of their transcripts. Our data provide novel molecular insights into the biological functions of STAT1 in the various cells composing the endometrium during maternal pregnancy recognition and implantation.
KW - cattle
KW - chromatin immunoprecipitation
KW - implantation
KW - transcription factor
KW - uterus.
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U2 - 10.1071/RD14034
DO - 10.1071/RD14034
M3 - Article
C2 - 25116692
AN - SCOPUS:84959352300
VL - 28
SP - 459
EP - 474
JO - Reproduction, Fertility and Development
JF - Reproduction, Fertility and Development
SN - 1031-3613
IS - 4
ER -