A PREGNANCY-ASSOCIATED GLYCOPROTEIN (PAG) UNIQUE TO THE ROE DEER (CAPREOLUS CAPREOLUS) AND ITS ROLE IN THE TERMINATION OF EMBRYONIC DIAPAUSE AND MATERNAL RECOGNITION OF PREGNANCY

2005 ◽  
Vol 51 (1) ◽  
pp. 1-11 ◽  
Author(s):  
ROGER T. LAMBERT
2019 ◽  
Vol 1 (4) ◽  
pp. 158-167 ◽  
Author(s):  
Vera A. Van der Weijden ◽  
Anna-Katharina Hankele ◽  
Anna B. Rüegg ◽  
Marion Schmicke ◽  
Karoline Rehm ◽  
...  

Progesterone (P4) plays a pivotal role in maintenance of pregnancy in many mammalian species. Species-specific P4 metabolites have been shown to function as primary acting progestogen and the receptor binding capacity varies between species. The European roe deer (Capreolus capreolus) displays a 4-5 month period of embryonic diapause, which decouples fertilization from implantation. The majority of roe deer have two corpora lutea that secrete P4. No changes in P4 concentrations have been observed during pre-implantation embryo development. As 5α-DHP is known to play a major role during pregnancy in elephants and horses, we hypothesized that 5α-DHP functions as additional progestogen facilitating embryo reactivation. The profile of 11 progestogens was quantified in roe deer plasma over the course of diapause and resumption of embryo development including P4, 3α- and 3β-DHP, 20α- and 20β-DHP, 5α- and 5β-DHP, 3α,5α- and 3α,5β-THP, as well as 3β,5α- and 3β,5β-THP. While P4 was most abundant during diapause and resumption of development, 20α-DHP was the most abundant P4 metabolite. This is different than in pregnant elephants, where 5α-DHP was most abundant, and the luteal phase in cattle, where 3α,5α-THP was most abundant. With the exception of a weak correlation of 3β,5α-THP, none of the progestogens significantly correlated with embryonic development in the roe deer. Thus, plasma 5α-DHP does not seem to play a role in embryo reactivation. We propose that progestogens might contribute to priming the endometrium for supporting embryo development and preparation for implantation.


1995 ◽  
Vol 7 (3) ◽  
pp. 313 ◽  
Author(s):  
AP Flint

Ruminant and non-ruminant members of the Artiodactyla appear to use different mechanisms for the maternal recognition of pregnancy. In ruminants, the trophoblast of the developing blastocyst produces a characteristic Type I interferon of the interferon-tau family; this acts by blocking endometrial synthesis of the oxytocin receptor. A similar mechanism applies to domestic ruminants (sheep, cow, goat) and deer. In roe deer, which have embryonic diapause and are monoestrus, there is no requirement for a pre-implantation blastocyst signal to ensure maternal recognition of pregnancy. This paper compares the mechanisms leading to the maternal recognition of pregnancy in ruminants with that suggested to occur in a non-ruminant (the domestic pig).


2021 ◽  
Vol 33 (2) ◽  
pp. 76
Author(s):  
Vera A. van der Weijden ◽  
Anna B. Rüegg ◽  
Sandra M. Bernal-Ulloa ◽  
Susanne E. Ulbrich

In species displaying embryonic diapause, the developmental pace of the embryo is either temporarily and reversibly halted or largely reduced. Only limited knowledge on its regulation and the inhibition of cell proliferation extending pluripotency is available. In contrast with embryos from other diapausing species that reversibly halt during diapause, embryos of the roe deer Capreolus capreolus slowly proliferate over a period of 4–5 months to reach a diameter of approximately 4mm before elongation. The diapausing roe deer embryos present an interesting model species for research on preimplantation developmental progression. Based on our and other research, we summarise the available knowledge and indicate that the use of embryonic stem cells (ESCs) would help to increase our understanding of embryonic diapause. We report on known molecular mechanisms regulating embryonic diapause, as well as cellular dormancy of pluripotent cells. Further, we address the promising application of ESCs to study embryonic diapause, and highlight the current knowledge on the cellular microenvironment regulating embryonic diapause and cellular dormancy.


2017 ◽  
Vol 46 (6) ◽  
pp. 582-591
Author(s):  
M. Beyes ◽  
N. Nause ◽  
M. Bleyer ◽  
F.-J. Kaup ◽  
S. Neumann

Rangifer ◽  
1999 ◽  
Vol 19 (1) ◽  
pp. 41 ◽  
Author(s):  
Roger T. Lambert

<p>Abstract: Roe deer blastocysts exhibit obligate embryonic diapause between early August and late December. The blastocyst then expands and elongates rapidly before implantation. The objective of this study was to ascertain the cues for reactivation of the diapausing blastocyst. Blood samples and reproductive tracts were collected from roe does during diapause, blastocyst expansion and subsequent implantation. Peripheral concentrations of oestradiol-17/3, progesterone and prolactin were measured by radioimmunoassay. Luteal progesterone release was determined following in vitro incubation. Conceptuses and endometrial tissue were cultured with 3H-leucine for 24 hours to measure de novo synthesis of secretory proteins. Endometrial secretory proteins were separated by two-dimensional electrophoresis. Results showed that peripheral progesterone concentrations declined by 55% just prior to expansion and did not rise until a 3-fold increase after implantation. Luteal progesterone release remained constant until expansion when it declined by 50% before increasing 2-fold at elongation and implantation. Concentrations of oestradiol-17/3 remained at a consistently low level during diapause and expansion until a 30-fold increase at elongation with concentrations remaining elevated after implantation. Plasma prolactin levels remained at basal concentrations during late diapause and then increased marginally at reactivation before decreasing again at elongation and implantation. Incorporation of radiolabel into both conceptus and endometrial secretory proteins was low during diapause, but incorporation in the conceptus increased 4&not;fold at expansion and by 24-fold at the expanded trophoblast stage. Incorporation into endometrial secretoty proteins remained constant until the expanded trophoblast stage and implantation when a 2-fold increase was recorded. Furthermore, the profile of endometrial secretory proteins was constant during diapause and expansion but changed qualitatively following implantation. These data indicate that both endometrial protein synthesis and sectetion did not change during late diapause and early expansion. The increase in conceptus protein synthesis not only precedes that of the endometrium but consistently low luteal progesterone release, peripheral progesterone and oestradioi-17/J concentrations at early expansion suggests that reactivation is not in response to a maternal uterine trigger.</p>


2020 ◽  
Vol 68 (1) ◽  
pp. 100
Author(s):  
Jan Demesko ◽  
Marta Kurek ◽  
Patrycja Podlaszczuk ◽  
Janusz Markowski

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