Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young Mice

Background To assess embryos derived by the transfer of meiosis-II chromosomes (M-II-t) from aged mice oocytes into ooplasms from younger mice to overcome the problem of age-related decline in female fertility. Materials and methods The developmental capacity karyotype and ultrastructure of recons...

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Main Authors: Abdolhossein Shahverdi, Mansoureh Movahedin, Mojtaba Rezazadeh Valojerdi, Hossein Baharvand
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2010-02-01
Series:International Journal of Fertility and Sterility
Subjects:
Online Access:http://www.ijfs.ir/article_45794_e793c9b79a4707109057d2ebd1bd0071.pdf
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spelling doaj-4bb488c7bc824388890075ad9072a0fe2020-11-25T04:03:58ZengRoyan Institute (ACECR), TehranInternational Journal of Fertility and Sterility2008-076X2008-07782010-02-013416517010.22074/ijfs.2010.4579445794Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young MiceAbdolhossein Shahverdi0Mansoureh Movahedin1Mojtaba Rezazadeh Valojerdi2Hossein Baharvand3Embryology Department, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran Anatomy Department, Medical Science Faculty, Tarbiat Modares University, Tehran, IranEmbryology Department, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, IranEmbryology Department, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran Anatomy Department, Medical Science Faculty, Tarbiat Modares University, Tehran, IranStem Cells and Developmental Biology Department, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran Developmental Biology Department, University of Science and Culture, ACECR, Tehran, IranBackground To assess embryos derived by the transfer of meiosis-II chromosomes (M-II-t) from aged mice oocytes into ooplasms from younger mice to overcome the problem of age-related decline in female fertility. Materials and methods The developmental capacity karyotype and ultrastructure of reconstructed oocytes derived from meiosis-II chromosome transplantation from aged mice into the ooplasms of young mice by piezo-micromanipulation were assessed. Results The survival rate of enucleated young oocytes was 54% and the percent of fertilized reconstructed oocytes was 23%. The rate of embryo development to the two-cell stage after cultivation was 40%. Since 82.4% of the analyzed embryos derived from reconstructed oocytes had condensed nuclei it was not possible to analyze their chromosomal integrity. However 17.6% of analyzable reconstructed old oocyte derived embryos (old-ODEs) had normal diploid sets of chromosomes. Major structural differences were not observed between young old and M-II-t derived two-cell embryos. Conclusion Our findings suggested that ooplasms from younger mice may overcome ageassociated problems in older mice.http://www.ijfs.ir/article_45794_e793c9b79a4707109057d2ebd1bd0071.pdfagingchromosomenuclear transferoocyteultrastructure
collection DOAJ
language English
format Article
sources DOAJ
author Abdolhossein Shahverdi
Mansoureh Movahedin
Mojtaba Rezazadeh Valojerdi
Hossein Baharvand
spellingShingle Abdolhossein Shahverdi
Mansoureh Movahedin
Mojtaba Rezazadeh Valojerdi
Hossein Baharvand
Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young Mice
International Journal of Fertility and Sterility
aging
chromosome
nuclear transfer
oocyte
ultrastructure
author_facet Abdolhossein Shahverdi
Mansoureh Movahedin
Mojtaba Rezazadeh Valojerdi
Hossein Baharvand
author_sort Abdolhossein Shahverdi
title Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young Mice
title_short Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young Mice
title_full Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young Mice
title_fullStr Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young Mice
title_full_unstemmed Evaluation of Embryos Derived from in vitro Fertilized Oocytes Reconstructed by Meiosis-II Chromosome Transplantation from Aged Mice to Ooplasms of Young Mice
title_sort evaluation of embryos derived from in vitro fertilized oocytes reconstructed by meiosis-ii chromosome transplantation from aged mice to ooplasms of young mice
publisher Royan Institute (ACECR), Tehran
series International Journal of Fertility and Sterility
issn 2008-076X
2008-0778
publishDate 2010-02-01
description Background To assess embryos derived by the transfer of meiosis-II chromosomes (M-II-t) from aged mice oocytes into ooplasms from younger mice to overcome the problem of age-related decline in female fertility. Materials and methods The developmental capacity karyotype and ultrastructure of reconstructed oocytes derived from meiosis-II chromosome transplantation from aged mice into the ooplasms of young mice by piezo-micromanipulation were assessed. Results The survival rate of enucleated young oocytes was 54% and the percent of fertilized reconstructed oocytes was 23%. The rate of embryo development to the two-cell stage after cultivation was 40%. Since 82.4% of the analyzed embryos derived from reconstructed oocytes had condensed nuclei it was not possible to analyze their chromosomal integrity. However 17.6% of analyzable reconstructed old oocyte derived embryos (old-ODEs) had normal diploid sets of chromosomes. Major structural differences were not observed between young old and M-II-t derived two-cell embryos. Conclusion Our findings suggested that ooplasms from younger mice may overcome ageassociated problems in older mice.
topic aging
chromosome
nuclear transfer
oocyte
ultrastructure
url http://www.ijfs.ir/article_45794_e793c9b79a4707109057d2ebd1bd0071.pdf
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