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Expression of renin-angiotensin system components in the early bovine embryo.
Pijacka, Wioletta; Hunter, Morag G; Broughton Pipkin, Fiona; Luck, Martin R.
Affiliation
  • Pijacka W; School of Biosciences University of Nottingham Sutton Bonington Campus, Loughborough, Leicestershire, LE12 5RD UK.
Endocr Connect ; 1(1): 22-30, 2012 Jul 01.
Article in En | MEDLINE | ID: mdl-23781300
ABSTRACT
The renin-angiotensin system (RAS), mainly associated with the regulation of blood pressure, has been recently investigated in female reproductive organs and the developing foetus. Angiotensin II (Ang II) influences oviductal gamete movements and foetal development, but there is no information about RAS in the early embryo. The aim of this study was to determine whether RAS components are present in the pre-implantation embryo, to determine how early they are expressed and to investigate their putative role at this stage of development. Bovine embryos produced in vitro were used for analysis of RAS transcripts (RT-PCR) and localisation of the receptors AGTR1 and AGTR2 (immunofluorescent labelling). We also investigated the effects of Ang II, Olmesartan (AGTR1 antagonist) and PD123319 (AGTR2 antagonist) on oocyte cleavage, embryo expansion and hatching. Pre-implanted embryos possessed AGTR1 and AGTR2 but not the other RAS components. Both receptors were present in the trophectoderm and in the inner cell mass of the blastocyst. AGTR1 was mainly localised in granular-like structures in the cytoplasm, suggesting its internalisation into clathrin-coated vesicles, and AGTR2 was found mainly in the nuclear membrane and in the mitotic spindle of dividing trophoblastic cells. Treating embryos with PD123319 increased the proportion of hatched embryos compared with the control. These results, the first on RAS in the early embryo, suggest that the pre-implanted embryo responds to Ang II from the mother rather than from the embryo itself. This may be a route by which the maternal RAS influences blastocyst hatching and early embryonic development.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Endocr Connect Year: 2012 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Endocr Connect Year: 2012 Document type: Article
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