91 Invivo- and invitro-produced bovine embryos have different microRNA profiles after invitro individual culture

2020 ◽  
Vol 32 (2) ◽  
pp. 171
Author(s):  
A. Bridi ◽  
I. Motta ◽  
G. Andrade ◽  
M. Del Collado ◽  
A. Ávila ◽  
...  

Invivo- and invitro-produced bovine embryos have different metabolic characteristics, embryonic development, and gene transcription. Additionally, pregnancy rates at 30 days (on average 51% and 34% when using fixed-time AI and invitro production, respectively) are different in beef cattle. Between Days 8 and 17 of the oestrous cycle, concurrent with embryo-maternal recognition, is when 40% of embryonic losses occur. These losses may occur due to altered embryo-maternal cross-talk. MicroRNA (miRNA) can be involved in this communication; however, its potentially regulated pathways in invivo and invitro embryos on Day 9 are unknown. Our hypothesis is that bovine embryos produced invivo and invitro contain different miRNA profiles, even after invivo bovine embryo were invitro cultured. Cows had the follicular wave synchronized and were superovulated to produce invivo or invitro bovine embryos. For the invitro group, on Day −8 of the protocol, the dominant follicles were recovered by ovum pickup, and invitro embryo production was performed to obtain embryos. For the invivo group, on Day −8, the cows were inseminated 12 and 24h after GnRH analogue application and on Day 7 after expected oestrus, uterine flushing was performed to obtain the embryos. Embryos from both groups were individually cultured for 48h. Three pools (of 5 embryos each) per group were used for reverse transcription of miRNAs from total RNA using miScript II RT Kit (Qiagen). Relative levels of 383 bovine miRNAs were determined using the geometric mean of miR-99b, RNU43 snoRNA, and Hm/Ms/Rt U1 snRNA by RT-qPCR. Differences in relative levels of miRNAs were determined by Student's t-test. A total of 210 miRNAs were detected in invivo and invitro embryos, and 13 out of 210 were differently identified between the groups. In invivo embryos, 6 miRNAs were up-regulated, whereas 7 miRNAs were up-regulated in invitro embryos. TARGETSCAN software was used to identify genes predicted as modulated by each miRNA. The top 100 genes predicted were used to identify enriched pathways according to DAVID Bioinformatics Resources. The miRNAs (miR-129, miR-132, miR-155, miR-192, miR-215, and miR-377) up-regulated in invivo embryos modulated pathways that include signaling pathways regulating pluripotency of stem cells (16 genes), TGF-β (11), hippo (10), oestrogen (8), and cell cycle (7). Moreover, miR-23a, miR-338, miR-34a, miR-491, miR-92b, miR-940, and miR-1271, which were increased in invitro embryos, regulate PI3K-Akt (17 genes), signaling pathways regulating pluripotency of stem cells (10), oestrogen (9), toll-like receptor (9), Wnt (9), and HIF-1 (7). The results demonstrate that even after 48h of invitro culture, bovine embryos produced invivo and invitro have different miRNA profiles that modulate pathways associated with embryonic development on Day 9. Furthermore, these results suggest that bioactive molecules, such as miRNAs, can modify embryo-maternal cross-talk, depending on the environment where the embryos are produced. Funding was provided by FAPESP 2017/19681-9, 2014/22887-0, and 2018/13155-6.

2016 ◽  
Vol 28 (4) ◽  
pp. 482 ◽  
Author(s):  
Qi-En Yang ◽  
Manabu Ozawa ◽  
Kun Zhang ◽  
Sally E. Johnson ◽  
Alan D. Ealy

Protein kinase C (PKC) delta (PRKCD) is a member of the novel PKC subfamily that regulates gene expression in bovine trophoblast cells. Additional functions for PRKCD in early embryonic development in cattle have not been fully explored. The objectives of this study were to describe the expression profile of PRKCD mRNA in bovine embryos and to examine its biological roles during bovine embryo development. Both PRKCD mRNA and protein are present throughout early embryo development and increases in mRNA abundance are evident at morula and blastocyst stages. Phosphorylation patterns are consistent with detection of enzymatically active PRKCD in bovine embryos. Exposure to a pharmacological inhibitor (rottlerin) during early embryonic development prevented development beyond the eight- to 16-cell stage. Treatment at or after the 16-cell stage reduced blastocyst development rates, total blastomere numbers and inner cell mass-to-trophoblast cell ratio. Exposure to the inhibitor also decreased basal interferon tau (IFNT) transcript abundance and abolished fibroblast growth factor-2 induction of IFNT expression. Furthermore, trophoblast adhesion and proliferation was compromised in hatched blastocysts. These observations provide novel insights into PRKCD mRNA expression profiles in bovine embryos and provide evidence for PRKCD-dependent regulation of embryonic development, gene expression and post-hatching events.


2006 ◽  
Vol 18 (2) ◽  
pp. 195 ◽  
Author(s):  
J. H. Pryor ◽  
K. R. Bondioli ◽  
S. K. Wood ◽  
M. D. Givens ◽  
C. R. Looney

TrypLE™Express (1X; GIBCO, Grand Island, NY, USA) is a recombinant fungal trypsin-like protease that may provide an alternative to animal-origin trypsin for inactivation of embryo-associated virus. This experiment was designed as an embryo safety study to determine if different exposure times of TrypLE™Express on 7-day bovine in vitro-fertilized (IVF) embryos would inhibit normal embryonic development in vitro. Good quality oocytes were harvested from ovaries of slaughtered animals and matured in vitro (Looney et al. 1994 Theriogenology 41, 67). Oocytes were fertilized (Day 0) with frozen-thawed, Percoll-separated Brangus spermatozoa in TALP-fertilization medium for 18 h. Presumptive zygotes were cultured in 0.5 mL of G1.3/G2.3 medium (Lane et al. 2003 Theriogenology 60, 407) supplemented with 8 mg/mL of Pentex BSA (Serologicals Corporation, Norcorss, GA, USA) under oil for 3 days in a 5% CO2, 5% O2, 90% N2 humidified modular incubator (Billups-Rothenberg, Inc., Del Mar, CA, USA) at 38.5°C. On Day 4, embryos were washed and moved to new culture wells containing G2.3 medium. Cleavage rates of 74% (750/1014) from three replicates produced 322 viable embryos on Day 7 which were then evenly distributed by grade and stage into three treatment groups (1-, 5-, and 10-minute exposure times to TrypLE™Express). Embryos were washed in accordance with International Embryo Transfer Society standards (Stringfellow, IETS Manual, 1998, 79–84) substituting TrypLE™Express with phenol red for the porcine-origin trypsin. Washed embryos were cultured in G2.3 medium with hatched rates assessed at 24, 48, and 72 h. Hatched embryos were fixed and stained using a modified Hoechst method (Damiani et al. 1996 Mol. Reprod. Dev. 45, 521–534) to count cells. The results are presented in Table 1. There were no significant differences (P < 0.05, chi-square analysis) between treatment groups for hatched rates or average cell counts. The results indicate that exposure to TrypLE™Express did not inhibit normal embryonic development. The efficacy of TrypLE™Express to remove or inactivate certain embryo-associated viruses is being investigated. Establishing an appropriate protocol for treatment of bovine embryos with TrypLE™Express will depend on the safety and efficacy of exposing embryos to this recombinant protease. Table 1. Comparison of hatched IVF bovine embryo rates and average cell counts after exposure to TrypLE™Express This work was funded by Invitrogen Corporation.


1998 ◽  
Vol 10 (8) ◽  
pp. 627 ◽  
Author(s):  
Teija T. Peura ◽  
Alan O. Trounson

The terms recycling and serial transfer refer to the use of cells from nuclear transfer embryos as a source of donor nuclei for a subsequent round of nuclear transfer. This approach has two benefits: improved reprogramming of the donor nucleus and an increase in absolute numbers of identical offspring. The beneficial effect of sequential exposure of donor nuclei to the early cytoplasm has been proven in several species, including amphibia, mice and cattle. Transferable embryos and live offspring have also been obtained from cattle and goat embryos produced by three and five rounds of nuclear transfer respectively. Although the limits to recycling have not been determined, embryonic development has been obtained from up to 10 cycles of nuclear transfer. Our results do not indicate differences in the embryonic developmental competence between clones from three generations in bovine embryo recycling. Although one live offspring from the second generation and pregnancies from third generation clones have been obtained, overall lower pregnancy rates and higher fetal losses than from first generation clones have been observed. Application of a novel vitrification method to nuclear transfer recycling removes many of the practical limitations of the technology.


Author(s):  
Yasemin Basbinar ◽  
Tugba Uysal ◽  
Caner Karaca ◽  
Ezgi Daskin ◽  
Hanife Ecenur Meco ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
M. Cenariu ◽  
E. Pall ◽  
C. Cernea ◽  
I. Groza

The purpose of this research was to evaluate three embryo biopsy techniques used for preimplantation genetic diagnosis (PGD) in cattle and to recommend the least invasive one for current use, especially when PGD is followed by embryo cryopreservation. Three hundred bovine embryos were biopsied by either one of the needle, aspiration or microblade method, and then checked for viability by freezing/thawing and transplantation to recipient cows. The number of pregnancies obtained after the transfer of biopsied frozen/thawed embryos was assessed 30 days later using ultrasounds. The results were significantly different between the three biopsy methods: the pregnancy rate was of 57% in cows that received embryos biopsied by needle, 43% in cows that received embryos biopsied by aspiration, and 31% in cows that received embryos biopsied by microblade. Choosing an adequate biopsy method is therefore of great importance in embryos that will undergo subsequent cryopreservation, as it significantly influences their viability after thawing.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Karina Cañón-Beltrán ◽  
Yulia N. Cajas ◽  
Serafín Peréz-Cerezales ◽  
Claudia L. V. Leal ◽  
Ekaitz Agirregoitia ◽  
...  

AbstractIn vitro culture can alter the development and quality of bovine embryos. Therefore, we aimed to evaluate whether nobiletin supplementation during EGA improves embryonic development and blastocyst quality and if it affects PI3K/AKT signaling pathway. In vitro zygotes were cultured in SOF + 5% FCS (Control) or supplemented with 5, 10 or 25 µM nobiletin (Nob5, Nob10, Nob25) or with 0.03% dimethyl-sulfoxide (CDMSO) during minor (2 to 8-cell stage; MNEGA) or major (8 to 16-cell stage; MJEGA) EGA phase. Blastocyst yield on Day 8 was higher in Nob5 (42.7 ± 1.0%) and Nob10 (44.4 ± 1.3%) for MNEGA phase and in Nob10 (61.0 ± 0.8%) for MJEGA phase compared to other groups. Mitochondrial activity was higher and lipid content was reduced in blastocysts produced with nobiletin, irrespective of EGA phase. The mRNA abundance of CDK2, H3-3B, H3-3A, GPX1, NFE2L2 and PPARα transcripts was increased in 8-cells, 16-cells and blastocysts from nobiletin groups. Immunofluorescence analysis revealed immunoreactive proteins for p-AKT forms (Thr308 and Ser473) in bovine blastocysts produced with nobiletin. In conclusion, nobiletin supplementation during EGA has a positive effect on preimplantation bovine embryonic development in vitro and corroborates on the quality improvement of the produced blastocysts which could be modulated by the activation of AKT signaling pathway.


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