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Molecular Approach in Understanding of Gametes and Embryos

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Biology".

Deadline for manuscript submissions: closed (31 July 2022) | Viewed by 6737

Special Issue Editors


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Guest Editor
Department of Human Reproduction, Division of Obstetrics and Gynecology, University Medical Center Ljubljana, 1000 Ljubljana, Slovenia
Interests: assisted reproduction; sperm; oocyte; embryo; ovary; testis; stem cells in reproduction; cryopreservation; blastocyst
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E-Mail Website
Guest Editor
1. Department of Human Reproduction, Division of Obstetrics and Gynecology, University Medical Center Ljubljana, 1000 Ljubljana, Slovenia
2. Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia
Interests: infertility; in vitro fertilization; assisted reproduction; oocyte; embryo; blastocyst; ovarian stimulation, endometriosis, fertility preservation, pregnancy, obesity

Special Issue Information

Dear Colleagues,

Gametes are highly specialized cells which undergo morphological and numerous complex molecular changes during development and differentiation. Changes in gametes on a molecular level can originate from the genetic code of these cells, but signals inducing development and behaviour of gametes can also be of extrinsic origin. For instance, gametes develop in close contact with somatic cells in various ways. Additionally, when gametes are used in IVF, extrinsic factors influencing their molecular state are culture media, handling approaches, and culture conditions. Recently, this aspect has received more attention, but there are still many gaps in understanding these conditions, and their importance is often overlooked in clinical practice. While gametes are special from a molecular aspect, the changes that these cells undergo after fertilization are even more profound. Two haploid cells merge and their genetic material has to find a way to start acting as one, which leads to dramatic and miraculous changes in the development of both embryos and organisms. The genetic status of embryos is often checked in IVF to select the most optimal embryo for transfer into uterus, but despite impressive development of such approach, it still faces many hurdles and is still a topic of controversy. While there is a focus on the genetics of embryos in IVF clinical practice, basic research on other levels, such as epigenetics, proteomics, metabolomics, secretomes, etc., has gained a mass of important data, helping to understand gametes and embryos on a molecular level. Thus, in the future, more attention should be paid to these approaches. On the one hand, this should be accomplished to improve our understanding of molecular state of gametes and embryos and, on the other hand, to improve clinical practice in IVF. While this Special Issue will be mainly focused on human reproduction, original papers and reviews of animal models are highly welcomed for submission.

Dr. Martin Stimpfel
Prof. Dr. Eda Vrtacnik-Bokal 
Guest Editors

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Keywords

  • in vitro fertilization
  • preimplantation genetic testing
  • aneuploidy
  • embryo
  • oocyte
  • sperm
  • meiosis
  • reproduction

Published Papers (2 papers)

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Research

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18 pages, 1408 KiB  
Article
Exopolysaccharide ID1 Improves Post-Warming Outcomes after Vitrification of In Vitro-Produced Bovine Embryos
by Erika Alina Ordóñez-León, Iris Martínez-Rodero, Tania García-Martínez, Manel López-Béjar, Marc Yeste, Elena Mercade and Teresa Mogas
Int. J. Mol. Sci. 2022, 23(13), 7069; https://doi.org/10.3390/ijms23137069 - 25 Jun 2022
Cited by 6 | Viewed by 1750
Abstract
This study aimed to assess the cryoprotectant role of exopolysaccharide (EPS) ID1, produced by Antarctic Pseudomonas sp., in the vitrification of in vitro-produced (IVP) bovine embryos. IVP day 7 (D7) and day 8 (D8) expanded blastocysts derived from cow or calf oocytes were [...] Read more.
This study aimed to assess the cryoprotectant role of exopolysaccharide (EPS) ID1, produced by Antarctic Pseudomonas sp., in the vitrification of in vitro-produced (IVP) bovine embryos. IVP day 7 (D7) and day 8 (D8) expanded blastocysts derived from cow or calf oocytes were vitrified without supplementation (EPS0) or supplemented with 10 µg/mL (EPS10) or 100 µg/mL (EPS100) EPS ID1. The effect of EPS ID1 was assessed in post-warming re-expansion and hatching rates, differential cell count, apoptosis rate, and gene expression. EPS100 re-expansion rates were significantly higher than those observed for the EPS0 and EPS10 treatments, regardless of culture length or oocyte source. EPS100 hatching rate was similar to the one of the fresh blastocysts except for those D7 blastocysts derived from calf oocytes. No differences were observed among EPS ID1 treatments when the inner cell mass, trophectoderm, and total cell number were assessed. Although apoptosis rates were higher (p ≤ 0.05) in vitrified groups compared to fresh embryos, EPS100 blastocysts had a lower number (p ≤ 0.05) of apoptotic nuclei than the EPS0 or EPS10 groups. No differences in the expression of BCL2, AQP3, CX43, and SOD1 genes between treatments were observed. Vitrification without EPS ID1 supplementation produced blastocysts with significantly higher BAX gene expression, whereas treatment with 100 µg/mL EPS ID1 returned BAX levels to those observed in non-vitrified blastocysts. Our results suggest that 100 µg/mL EPS ID1 added to the vitrification media is beneficial for embryo cryopreservation because it results in higher re-expansion and hatching ability and it positively modulates apoptosis. Full article
(This article belongs to the Special Issue Molecular Approach in Understanding of Gametes and Embryos)
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Review

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13 pages, 303 KiB  
Review
Non-Invasive Preimplantation Genetic Testing for Aneuploidy and the Mystery of Genetic Material: A Review Article
by Maja Tomic, Eda Vrtacnik Bokal and Martin Stimpfel
Int. J. Mol. Sci. 2022, 23(7), 3568; https://doi.org/10.3390/ijms23073568 - 25 Mar 2022
Cited by 11 | Viewed by 4567
Abstract
This review focuses on recent findings in the preimplantation genetic testing (PGT) of embryos. Different preimplantation genetic tests are presented along with different genetic materials and their analysis. Original material concerning preimplantation genetic testing for aneuploidy (PGT-A) was sourced by searching the PubMed [...] Read more.
This review focuses on recent findings in the preimplantation genetic testing (PGT) of embryos. Different preimplantation genetic tests are presented along with different genetic materials and their analysis. Original material concerning preimplantation genetic testing for aneuploidy (PGT-A) was sourced by searching the PubMed and ScienceDirect databases in October and November 2021. The searches comprised keywords such as ‘preimplantation’, ‘cfDNA’; ‘miRNA’, ‘PGT-A’, ‘niPGT-A’, ‘aneuploidy’, ‘mosaicism’, ‘blastocyst biopsy’, ‘blastocentesis’, ‘blastocoel fluid’, ‘NGS’, ‘FISH’, and ‘aCGH’. Non-invasive PGT-A (niPGT-A) is a novel approach to the genetic analysis of embryos. The premise is that the genetic material in the spent embryo culture media (SECM) corresponds to the genetic material in the embryo cells. The limitations of niPGT-A are a lower quantity and lesser quality of the cell-free genetic material, and its unknown origin. The concordance rate varies when compared to invasive PGT-A. Some authors have also hypothesized that mosaicism and aneuploid cells are preferentially excluded from the embryo during early development. Cell-free genetic material is readily available in the spent embryo culture media, which provides an easier, more economic, and safer extraction of genetic material for analysis. The sampling of the SECM and DNA extraction and amplification must be optimized. The origin of the cell-free media, the percentage of apoptotic events, and the levels of DNA contamination are currently unknown; these topics need to be further investigated. Full article
(This article belongs to the Special Issue Molecular Approach in Understanding of Gametes and Embryos)
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