scholarly journals Placental development during early pregnancy in sheep: Effects of embryo origin on fetal and placental growth and global methylation

2013 ◽  
Vol 79 (1) ◽  
pp. 94-102 ◽  
Author(s):  
Anna T. Grazul-Bilska ◽  
Mary Lynn Johnson ◽  
Pawel P. Borowicz ◽  
Loren Baranko ◽  
Dale A. Redmer ◽  
...  
Reproduction ◽  
2011 ◽  
Vol 141 (4) ◽  
pp. 529-540 ◽  
Author(s):  
Anna T Grazul-Bilska ◽  
Mary Lynn Johnson ◽  
Pawel P Borowicz ◽  
Megan Minten ◽  
Jerzy J Bilski ◽  
...  

To characterize early fetal placental development, gravid uterine tissues were collected from pregnant ewes every other day from day 16 to 30 after mating. Determination of 1) cell proliferation was based on Ki67 protein immunodetection; 2) global methylation was based on 5-methyl-cytosine (5mC) expression and mRNA expression for DNA methyltransferases (DNMTs)1,3a, and3b; and 3) vascular development was based on smooth muscle cell actin immunolocalization and on mRNA expression of several factors involved in the regulation of angiogenesis in fetal membranes (FMs). Throughout early pregnancy, the labeling index (proportion of proliferating cells) was very high (21%) and did not change. Expression of 5mC and mRNA forDNMT3bdecreased, but mRNA forDNMT1and3aincreased. Blood vessels were detected in FM on days 18–30 of pregnancy, and their number per tissue area did not change. The patterns of mRNA expression for placental growth factor, vascular endothelial growth factor, and their receptorsFLT1andKDR; angiopoietins 1 and 2 and their receptorTEK; endothelial nitric oxide synthase and the NO receptorGUCY13B; and hypoxia inducing factor 1 α changed in FM during early pregnancy. These data demonstrate high cellular proliferation rates, and changes in global methylation and mRNA expression of factors involved in the regulation of DNA methylation and angiogenesis in FM during early pregnancy. This description of cellular and molecular changes in FM during early pregnancy will provide the foundation for determining the basis of altered placental development in pregnancies compromised by environmental, genetic, or other factors.


Placenta ◽  
2016 ◽  
Vol 43 ◽  
pp. 77-80 ◽  
Author(s):  
K.E. Quinn ◽  
L.P. Reynolds ◽  
A.T. Grazul-Bilska ◽  
P.P. Borowicz ◽  
R.L. Ashley

2011 ◽  
Vol 1 (2) ◽  
pp. 22-29
Author(s):  
JJ Babu Geddam ◽  
Radhakrishna KV ◽  
Ramalaxmi BA ◽  
Balakrishna N ◽  
Qadri SSYH ◽  
...  

Reproduction ◽  
2010 ◽  
Vol 140 (1) ◽  
pp. 165-174 ◽  
Author(s):  
Anna T Grazul-Bilska ◽  
Pawel P Borowicz ◽  
Mary Lynn Johnson ◽  
Megan A Minten ◽  
Jerzy J Bilski ◽  
...  

Placental vascular development (angiogenesis) is critical for placental function and thus for normal embryonic/fetal growth and development. Specific environmental factors or use of assisted reproductive techniques may result in poor placental angiogenesis, which may contribute to embryonic losses and/or fetal growth retardation. Uterine tissues were collected on days 14, 16, 18, 20, 22, 24, 26, 28, and 30 after mating and on day 10 after estrus (nonpregnant controls) to determine vascular development and expression of several factors involved in the regulation of angiogenesis in the endometrium. Compared with controls, several measurements of endometrial vascularity increased (P<0.001) including vascular labeling index (LI; proportion of proliferating cells), the tissue area occupied by capillaries, area per capillary (capillary size), total capillary circumference per unit of tissue area, and expression of factor VIII (marker of endothelial cells), but capillary number decreased (P<0.001). Compared with controls, mRNA for placental growth factor, vascular endothelial growth factor receptors, angiopoietins (ANGPT) 1 and 2, ANGPT receptorTEK, endothelial nitric oxide synthase, and hypoxia-inducible factor 1α increased (P<0.05) during early pregnancy. Vascular LI was positively correlated (P<0.05) with several measurements of vascularity and with mRNA expression of angiogenic factors. These data indicate that endometrial angiogenesis, manifested by increased vascularity and increased expression of several factors involved in the regulation of angiogenesis, is initiated very early in pregnancy. This more complete description of early placental angiogenesis may provide the foundation for determining whether placental vascular development is altered in compromised pregnancies.


2020 ◽  
Vol 319 (3) ◽  
pp. E557-E561 ◽  
Author(s):  
Henry C. Ezechukwu ◽  
Cornelius A. Diya ◽  
Nirajan Shrestha ◽  
Deanne H. Hryciw

The endocannabinoid system (ECS) is associated with several physiological processes, including reproduction. This system consists of the cannabinoid receptors, endocannabinoid ligands, and enzymes that metabolize and degrade these fatty acids. Recent evidence shows that cannabinoid receptors are expressed in cells of the reproductive system, including endometrial stromal cells, ovaries, and sperm cells. Emerging and recent research suggests that the ECS may play a significant role in reproduction. The endocannabinoid ligands anandamide and 2-arachidonoylglycerol are crucial for successful endometrium decidualization, placental development, and embryo implantation. Alteration in cannabinoid receptor expression or in endocannabinoid homeostasis by excessive intake of cannabis during pregnancy is associated with negative pregnancy outcomes, including preterm birth. The use of medicinal cannabis is becoming more widespread in Western countries, especially in people of reproductive age. Cannabis contains phytocannabinoids, which modulate the ECS, and emerging evidence suggests that phytocannabinoids, through their action on cannabinoid receptors, may have a negative impact on fertility, pregnancy outcome, and fetal health. In this mini-review, we highlight the recent advances in the field, which explore the role of endocannabinoids in early pregnancy and the effects of excessive intake of phytocannabinoids in pregnancy outcomes.


2008 ◽  
Vol 12 (6a) ◽  
pp. 2295-2296 ◽  
Author(s):  
Karen Forbes ◽  
Lucy M. Hurst ◽  
J. Martin Gibson ◽  
John D. Aplin ◽  
Melissa Westwood

1981 ◽  
Vol 96 (1) ◽  
pp. 187-194 ◽  
Author(s):  
I. McDonald ◽  
J. J. Robinson ◽  
C. Fraser

SUMMARYThe weights of 44 twin foetuses, 99 triplets and 44 quadruplets, varying in gestational age from 55 to 145 days, were studied in relation to age, sex, litter size, uterine position, placental structure and weight, and ovulation rate. Triplet and quadruplet foetuses were more variable in weight, within litters, than were twins. The difference increased with foetal age and was attributed to increased competition between foetuses which were located within the same horn of the uterus. The effect was largely associated with differences in placental development, i.e. numbers of cotyledons and weight, but those differences did not entirely account for the reduction in foetal weight with increasing litter size. Differences in placental development, arising from embryo mortality, also accounted for the reduction in foetal weight when ovulation rate exceeded litter size. In contrast, differences in foetal weight associated with the sex of the foetuses were only partly mediated by differences in cotyledon weight. Foetuses in the larger litters are thus not only lighter in weight but are more variable in weight, the increased variability being controlled by events in early pregnancy.


2020 ◽  
Vol 27 (5) ◽  
pp. 411-418 ◽  
Author(s):  
Meiyu Qiu ◽  
Tao Li ◽  
Binhu Wang ◽  
Hongbin Gong ◽  
Tao Huang

Background: microRNAs (miRNAs) are a small, endogenous non-coding RNAs that are involved in post-transcriptional gene regulation of many biological processes, including embryo implantation and placental development. In our previous study, miR-146a-5p was found expressed higher in the serum exosomes of pregnant sows than non-pregnant. The research on miR-146a-5p has been mainly related to human diseases, but there are few studies on its effects on the reproduction of sows in early pregnancy. Objective: In this article, our motivation is to study the role of miR-146a-5p in the early pregnancy of sows on the cell proliferetion and apoptosis by targeting SMAD3 and SMAD4. Methods: Bioinformatics software was used to identify the target genes of miR-146a-5p. The wildtype and mutant-type recombinant plasmids of dual-luciferase reporter with 3'-UTR of Smad3 or 3'- UTR of Smad4 were constructed, and co-transfected in porcine kidney cell (PK-15 cell) with miR- 146a-5p mimic, mimic-NC(M-NC), inhibitor and inhibitor-NC(IN-NC), then dual-luciferase activity analysis, qRT-PCR and Western blot were performed to verify the target genes. After the transfection of BeWo choriocarcinoma cell (BeWo cell) with miR-146a-5p mimic, M-NC, inhibitor and IN-NC, the mRNA expression of Caspase-3, BAX and Bcl-2 was measured using qRT-PCR, and the cell proliferation was measured using CCK-8 kit. Results: The luciferase, mRNA and protein expression of Smad3 in PK-15 cells treated by Smad3- 3'-UTR-W co-transfected with miR-146a-5p mimic were significantly lower than that with miR- 146a-5p M-NC, and the results of Smad4 were similar to Smad3, but the protein expression had a trend to lower in mimic group. The expression level of Bcl-2 in the miR-146a-5p mimic group was significantly lower than that in the miR-146a-5p M-NC group, but the expression pattern of Caspase-3 was just opposite. The mimic of miR-146a-5p reduced the proliferation of BeWo cells, however the inhibitor increased. Conclusion: Smad3 and Smad4 are the direct target genes of miR-146a-5p. The expression of Smad3 and Smad4 were affected by the mimic and inhibitor of miR-146a-5p. miR-146a-5p affects cell apoptosis and proliferation by regulating their target genes. This study provided new data to understand the regulation mechanism of early pregnancy in sows.


Reproduction ◽  
2021 ◽  
Author(s):  
Veronika Tandl ◽  
Denise Hoch ◽  
Julia Bandres-Meriz ◽  
Sanela Nikodijevic ◽  
Gernot Desoye ◽  
...  

Endoplasmic reticulum (ER)-stress activates the unfolded protein response (UPR), which plays a (patho)physiological role in the placenta. Oxygen and hyperinsulinemia are major regulators of placental development. Thus, we hypothesized that oxygen, insulin and their interplay modulate ER-stress in early pregnancy. Using the human first trimester trophoblast cell line ACH-3P, we quantified mRNA and protein of several members of UPR by RT-qPCR and Western blotting, respectively. ER-stress induction using tunicamycin and brefeldin A resulted in increased CHOP (4.6-fold change; P ≤ 0.001), XBP1 expression (1.7- and 1.3-fold change, respectively; P ≤ 0.001 and P < 0.05) and XBP1 splicing (7.9- and 12.8-fold change, respectively; P ≤ 0.001). We subsequently analyzed the effect of oxygen (6.5%, 2.5%), insulin (0.1-10 nM) and their interaction using ANCOVA adjusted for cell passage as co-variate. Although GRP78 protein remained unaffected, low oxygen (2.5% O2) increased IRE1α phosphorylation (+52%; P < 0.05) and XBP1 splicing (1.8-fold change; P ≤ 0.001) after 24h, while eIF2α protein and CHOP expression were downregulated (–28%; P < 0.05 and –24%; P ≤ 0.001; respectively). eIF2α phosphorylation was also reduced after 48h by low oxygen (–61%; P < 0.05), but increased in the presence of insulin (+46%; P ≤ 0.01). These changes were not PERK-mediated, since PERK phosphorylation and total protein were not altered. Overall, our results suggest that IRE1α and eIF2α UPR-pathways are differentially regulated by oxygen and insulin in early pregnancy.


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