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      Mimicking Mother Nature in the Field of Human Reproduction?

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          Abstract

          Dear Editor, Although humans have made significant progress in understanding reproductive events, nature still has more information to reveal. Towards the end of the 19 th century, humans started studying reproductive processes such as gametogenesis, fertilization, and embryo development. 1 Since sperm and egg roles in fertilization were introduced in 1870 for the first time, reproductive biologists tried to emulate the natural reproductive processes despite the significant lack of knowledge regarding in vivo reproductive mechanisms. In the quest to mimic or overcome natural reproduction processes, numerous attempts have been made to produce embryos from non-germ cells. 2 3 These trials ultimately culminated in the birth of Dolly the sheep 4 as a result of somatic cell nuclear transfer, starting a new era of cloning or asexual reproduction. Though not fully understood at the time (1959), the work of Chang 5 regarding the fertilization of rabbit ova in vitro , paved the way for the application of artificial reproductive techniques (ART) in humans. Ever since then, it has always been considered that the best evidence for these technologies to be accepted is that the progeny derived from ART are capable of reproducing naturally, especially those conceived by in vitro fertilization (IVF). Researchers have tried to ensure in vitro maturation of the spermatogonial stem cells transplanted in testes, separated into small pieces, and cultured on agarose, which migrated towards the basal membrane and settled on it, as in the in vivo process. 6 On the other hand, have reported that after ovary tissue cryopreservation and orthotopic transplantation result in a 76% spontaneous pregnancy live baby rate in 119 human females 13 out 119 of these patients need also in vitro maturation of the oocytes, 7 which allows to postulate that the cryopreservation of ovarian tissue could be a promising method to preserve fertility in humans. However, transformation of the experience and data obtained from animals to humans has been failing. Researchers hope that during these in vitro processes, all the cellular events occur in exactly the same fashion as to mimic the in vivo scenario, ultimately resulting in new births. Hence, the importance of demonstrating that Dolly could produce offspring through natural mating. Consequently, the potential for humans to produce offspring from gametes generated in vitro is exciting, but in some way rather pretentious as it assumes that the events that happen in vitro are the same as those that occur in vivo . It is undeniable that all these reproductive developments have amazed society. Although there is plenty of literature supporting the possibility, there are still many key questions to be resolved, such as “What minimum number of cells to obtain a blastocyst to obtain a pregnancy, what is the relationship between the number of cells required to obtain a favorable result?”, “In case of cloning how many nuclei are needed to be injected to produce an embryo?” or the efficiency and scalability of such methods to produce enough gametes for assisted conception treatments and will they be safe to use? Undeniably it appears as if Mother Nature is reminding humans that we are still far from replicating the efficiency of natural reproduction. Louise Brown, the first human born through IVF (test-tube baby), is currently 43 years old and has two living children of her own from natural birth. However, more research is required to obtain better success rates and ensure these in vitro processes are safe in all aspects. 8 In cattle, procedures involving in vitro oocyte maturation and embryo production find it difficult to achieve 40 births from 100 embryos. Furthermore, to create 100 embryos, it is necessary to start with about 400 oocytes 9 ; thus, a 10-fold reduction is experienced: 400 oocytes leading to 40 births. Considering the inefficiency of in vitro produced embryos and the response of gametes it is about one-hundredth of that obtained by naturally produced gametes and conditions. 10 An explanation could be associated with the fact that bovine blastocysts obtained in vitro have fewer cells than their in vivo counterparts. 9 On the other hand, another example, is the need to use thousands of parental cells to obtain few colonies with spermatogenesis inside the testis, although systems should allow the generation of a larger number every day. 3 It would seem very obvious to believe that researchers have been appropriating step by step every event that nature allows them to know. Two works were recently published on the generation of embryo-like structures “the first synthetic embryo" going over the interaction between intergametes: spermatozoa and oocytes. 11 12 The living structures are expected to further a deep understanding of embryogenesis. Finally, once the problem is fully understood, as described earlier (i.e. all events contributing as a unit in its entirety), it can be concluded that nature shows plasticity on a daily basis. In the end, nature will reveal its answers progressively as knowledge translates into understanding. Ultimately it is almost as if we were to engage in dialogue with Mother Nature and asked her to reveal her secrets based on our knowledge and understanding of live births, matured eggs, spermatozoa, and oocytes potentially derived from different cell types. However, nature always has the upper hand and it is as if she would respond with: "Only when you are capable of matching some of my processes, I will let you in on the next secret step. However, it is clear that there is still a long way to go because your way of thinking possibly is not correct. Once you understand all the possibilities, you will increase the efficiency of each process you are interested in”. The advances in knowledge and control of reproductive events during the preceding 100 years are undeniable, but to try and mimic nature and expect similar results and outcomes we have to make a fundamental paradigm shift in how we approach the problem at hand. When it comes to interventions and reproduction processes in humans and other species, acceptable milestones have been achieved but that does not imply that all are acceptable and good.

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          Viable offspring derived from fetal and adult mammalian cells.

          Fertilization of mammalian eggs is followed by successive cell divisions and progressive differentiation, first into the early embryo and subsequently into all of the cell types that make up the adult animal. Transfer of a single nucleus at a specific stage of development, to an enucleated unfertilized egg, provided an opportunity to investigate whether cellular differentiation to that stage involved irreversible genetic modification. The first offspring to develop from a differentiated cell were born after nuclear transfer from an embryo-derived cell line that had been induced to become quiescent. Using the same procedure, we now report the birth of live lambs from three new cell populations established from adult mammary gland, fetus and embryo. The fact that a lamb was derived from an adult cell confirms that differentiation of that cell did not involve the irreversible modification of genetic material required for development to term. The birth of lambs from differentiated fetal and adult cells also reinforces previous speculation that by inducing donor cells to become quiescent it will be possible to obtain normal development from a wide variety of differentiated cells.
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            Reconstitution of the mouse germ cell specification pathway in culture by pluripotent stem cells.

            The generation of properly functioning gametes in vitro requires reconstitution of the multistepped pathway of germ cell development. We demonstrate here the generation of primordial germ cell-like cells (PGCLCs) in mice with robust capacity for spermatogenesis. PGCLCs were generated from embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) through epiblast-like cells (EpiLCs), a cellular state highly similar to pregastrulating epiblasts but distinct from epiblast stem cells (EpiSCs). Reflecting epiblast development, EpiLC induction from ESCs/iPSCs is a progressive process, and EpiLCs highly competent for the PGC fate are a transient entity. The global transcription profiles, epigenetic reprogramming, and cellular dynamics during PGCLC induction from EpiLCs meticulously capture those associated with PGC specification from the epiblasts. Furthermore, we identify Integrin-β3 and SSEA1 as markers that allow the isolation of PGCLCs with spermatogenic capacity from tumorigenic undifferentiated cells. Our findings provide a paradigm for the first step of in vitro gametogenesis. Copyright © 2011 Elsevier Inc. All rights reserved.
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              Embryo model completes gastrulation to neurulation and organogenesis

              Embryonic stem (ES) cells can undergo many aspects of mammalian embryogenesis in vitro 1 – 5 , but their developmental potential is substantially extended by interactions with extraembryonic stem cells, including trophoblast stem (TS) cells, extraembryonic endoderm stem (XEN) cells and inducible XEN (iXEN) cells 6 – 11 . Here we assembled stem cell-derived embryos in vitro from mouse ES cells, TS cells and iXEN cells and showed that they recapitulate the development of whole natural mouse embryo in utero up to day 8.5 post-fertilization. Our embryo model displays headfolds with defined forebrain and midbrain regions and develops a beating heart-like structure, a trunk comprising a neural tube and somites, a tail bud containing neuromesodermal progenitors, a gut tube, and primordial germ cells. This complete embryo model develops within an extraembryonic yolk sac that initiates blood island development. Notably, we demonstrate that the neurulating embryo model assembled from Pax6 -knockout ES cells aggregated with wild-type TS cells and iXEN cells recapitulates the ventral domain expansion of the neural tube that occurs in natural, ubiquitous Pax6 -knockout embryos. Thus, these complete embryoids are a powerful in vitro model for dissecting the roles of diverse cell lineages and genes in development. Our results demonstrate the self-organization ability of ES cells and two types of extraembryonic stem cells to reconstitute mammalian development through and beyond gastrulation to neurulation and early organogenesis. Synthetic mouse embryos assembled from embryonic stem cells, trophoblast stem cells and induced extraembryonic endoderm stem cells closely recapitulate the development of wild-type and mutant natural mouse embryos up to embryonic day 8.5.
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                Author and article information

                Journal
                Rev Bras Ginecol Obstet
                Rev Bras Ginecol Obstet
                10.1055/s-00030576
                RBGO Gynecology & Obstetrics
                Thieme Revinter Publicações Ltda. (Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil )
                0100-7203
                1806-9339
                27 April 2023
                March 2023
                1 April 2023
                : 45
                : 3
                : 159-160
                Affiliations
                [1 ]Universidad Nacional de Colombia, Sede Orinoquia, Arauca, Colombia
                [2 ]Reproduction Group, Department of Microbiology and Parasitology, Medical School, University of Antioquia, Antioquia, Colombia
                [3 ]Nuffield Department of Women's & Reproductive Health, University of Oxford, Women's Centre, Level 3, John Radcliffe Hospital, Oxford
                [4 ]Department of Basic Sciences, College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates
                [5 ]Division of Medical Physiology, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa
                Author notes
                Address for correspondence Walter D. Cardona Maya, PhD Reproduction Group, Department of Microbiology and Parasitology, Medical School, University of Antioquia AntioquiaColombia wdario.cardona@ 123456udea.edu.co
                Author information
                http://orcid.org/0000-0002-1556-6387
                http://orcid.org/0000-0002-0001-1821
                http://orcid.org/0000-0003-4617-4367
                http://orcid.org/0000-0003-0062-6444
                Article
                220341
                10.1055/s-0043-1768460
                10139770
                37105200
                bced108a-7ec7-4f84-92a5-9c8d6258e379
                Federação Brasileira de Ginecologia e Obstetrícia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ )

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 November 2022
                : 02 December 2022
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