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      Comparison of the rates for reaching the blastocyst stage between normal and abnormal pronucleus embryos monitored by a time-lapse system in IVF patients

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          Abstract

          Objective:

          To compare the rates of blastocyst stage development between embryos fertilized after one (MPN) or more than two pronucleus (PN) (3PN, 4PN-multiPN) with those after 2PN in the same patients.

          Material and Methods:

          The embryos of patients who had both abnormal PN (MPN, 3PN or 4PN) and normal fertilized (2PN) embryos after intracytoplasmic sperm injection (ICSI) fertilization, were followed with a time-lapse system following the ICSI procedure. The rates of reaching the blastocyst stage were compared between normal and abnormally fertilized embryos.

          Results:

          One thousand eight hundred and twenty oocytes were collected from 140 patients and 1280 (70.3%) of them were fertilized. MPN, 2PN and 3PN, 4PN (multiPN) ratios of the embryos in the pronuclear stage were 11.4%, 83.13% and 5.47%, respectively. The rates of reaching the blastocyst stage among these embryos were 17.1%, 60.8% and 42.8% for MPN, 2PN and multiPN, respectively. The proportion reaching blastocyst development was significantly higher following 2PN compared to those after MPN and multiPN (p<0.05). Embryos developing after multiPN had significantly higher rates of reaching the blastocyst stage compared to those after MPN (p<0.01).

          Conclusion:

          The majority of abnormally pronucleated embryos arrest without reaching the blastocyst stage. MultiPN embryos have a higher rate of blastocyst development than MPN embryos.

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          Most cited references38

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          Embryonic stem cell lines from human blastocysts: somatic differentiation in vitro.

          We describe the derivation of pluripotent embryonic stem (ES) cells from human blastocysts. Two diploid ES cell lines have been cultivated in vitro for extended periods while maintaining expression of markers characteristic of pluripotent primate cells. Human ES cells express the transcription factor Oct-4, essential for development of pluripotential cells in the mouse. When grafted into SCID mice, both lines give rise to teratomas containing derivatives of all three embryonic germ layers. Both cell lines differentiate in vitro into extraembryonic and somatic cell lineages. Neural progenitor cells may be isolated from differentiating ES cell cultures and induced to form mature neurons. Embryonic stem cells provide a model to study early human embryology, an investigational tool for discovery of novel growth factors and medicines, and a potential source of cells for use in transplantation therapy.
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            Cell death in the mammalian blastocyst.

            Cell death is a widespread feature in the blastocysts of many mammals. Isolated cells in both the inner cell mass and the trophectoderm undergo cell death. These dying cells appear morphologically to be undergoing apoptosis. In mouse blastocysts, a wave of cell death is seen in vivo, suggesting that it plays an important role in normal development. However, cell death is increased under suboptimal culture conditions. There is evidence that levels of cell death are regulated by 'survival' factors produced both by the embryo itself and by the maternal reproductive tract. The role of cell death in development is unknown, but could involve the elimination of abnormal cells, or a sublineage of cells with an inappropriate developmental potential. Work in other systems has demonstrated that cell death is regulated by the activity of apoptosis genes. Whether these genes are implicated in blastocyst cell death, and the reasons for apoptosis in the early embryo, remain to be determined.
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              Fertilization failures and abnormal fertilization after intracytoplasmic sperm injection.

              This study addresses the incidence of failed (0%) and suboptimal ( 50% fertilization in every cycle. Only 26% of the couples had 50% variation. The causes of failed and abnormal fertilization were studied in unfertilized and abnormally fertilized oocytes after staining with Hoechst 33342. In total, 1005 unfertilized oocytes were studied, of which 828 (82%) were still at metaphase II and 177 (18%) were activated. Most of the oocytes (83%) contained a spermatozoon and, in the majority of these oocytes, the sperm head was partially or completely decondensed. Hence, failure of oocyte activation was the principal cause of fertilization failure. A similar pattern was observed in activated, unfertilized oocytes, although there was a higher incidence of intact spermatozoa in these oocytes compared with metaphase II, unfertilized oocytes. Interestingly, 56% of the activated oocytes contained a decondensed sperm head which was not processed into a male pronucleus. A total of 169 abnormally fertilized oocytes was also studied. Two anomalies were found: digyny due to retention of the second polar body and its subsequent transformation into a third pronucleus, and abnormal pronuclear size and number.
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                Author and article information

                Journal
                J Turk Ger Gynecol Assoc
                J Turk Ger Gynecol Assoc
                JTGGA
                Journal of the Turkish German Gynecological Association
                Galenos Publishing
                1309-0399
                1309-0380
                June 2021
                28 May 2021
                : 22
                : 2
                : 120-126
                Affiliations
                [1 ]PhD Student, Institute of Health Sciences, İstanbul Medipol University, İstanbul, Turkey
                [2 ]Department of Histology and Embryology, Maltepe University Faculty of Medicine, İstanbul, Turkey
                [3 ]Department of Obstetrics and Gynecology, Acıbadem Mehmet Ali Aydınlar University Faculty of Medicine, İstanbul, Turkey
                [4 ]Unit of ART, Acıbadem Altunizade Hospital, İstanbul, Turkey
                Author notes
                * Address for Correspondence: E-mail: bselam@ 123456hotmail.com
                Author information
                https://orcid.org/0000-0001-6440-0984
                https://orcid.org/0000-0002-0717-1756
                https://orcid.org/0000-0003-4478-7514
                https://orcid.org/0000-0002-3397-7980
                https://orcid.org/0000-0001-7870-3687
                Article
                41604
                10.4274/jtgga.galenos.2020.2020.0033
                8187983
                33041260
                bd56a799-06bb-4d7d-a8c6-44a338d9ad9e
                © Copyright 2021 by the Turkish-German Gynecological Education and Research Foundation

                Journal of the Turkish-German Gynecological Association published by Galenos Publishing House.

                History
                : 12 March 2020
                : 20 July 2020
                Categories
                Original Investigation

                blastocyst,icsi,mpn,multipn,time-lapse
                blastocyst, icsi, mpn, multipn, time-lapse

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