Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro Maturation

SUMMARY: Vitrification is a physical process in which the concentrated cryoprotectant solution after exposure to extreme cold without ice crystal formation in living cells to be converted glassing state. In this study, maturation rate and ultrastructure of mouse oocytes followed by vitrification bef...

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Autores principales: Izadi,Maryam, Eftekhar-Vaghefi,Seyed Hassan, Akbari,Hakimeh, Asadi-Shekari,Majid, Mokhtari,Tahmineh
Lenguaje:English
Publicado: Sociedad Chilena de Anatomía 2018
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022018000100180
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spelling oai:scielo:S0717-950220180001001802019-09-16Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro MaturationIzadi,MaryamEftekhar-Vaghefi,Seyed HassanAkbari,HakimehAsadi-Shekari,MajidMokhtari,Tahmineh Vitrification Fertility preservation Cryopreservation In Vitro Maturation Ultrastructure SUMMARY: Vitrification is a physical process in which the concentrated cryoprotectant solution after exposure to extreme cold without ice crystal formation in living cells to be converted glassing state. In this study, maturation rate and ultrastructure of mouse oocytes followed by vitrification before or after in-virto maturation (IVM) were evaluated. A total of 373 germinal vesicle oocytes were obtained from ovaries and divided into three fresh IVM, IVM vitrified, vitrified IVM groups. Ten metaphase II oocytes were obtained from uterine tubes and considered as the control group. Oocytes in vitrified groups were vitrified by Cryotop using vitrification medium and kept in liquid nitrogen. The maturation media was a-MEM supplemented with rFSH + hCG. After 24-48 h of incubation, the oocytes were investigated for nuclear maturation and ultrastructural changes using transmission electron microscopy (TEM). The oocyte maturation rate in vIVM group was significantly lower than IVMv group, when the two groups were compared with vIVM had the highest maturity. The evaluation ultrastructure of the four groups showed that the number of cortical granules, microvilli and mitochondria-SER aggregates in vIVM group were lowest and the highest amongst the number of vacuoles. Zona pellucida was darker than the control group in two freeze groups vIVM and IVMv. Most similar groups to the control group were group vIVM, Group IVMv and ultimately vIVM group, respectively. According to the results, IVM procedure is more efficient when it is performed before oocyte vitrification.info:eu-repo/semantics/openAccessSociedad Chilena de AnatomíaInternational Journal of Morphology v.36 n.1 20182018-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022018000100180en10.4067/S0717-95022018000100180
institution Scielo Chile
collection Scielo Chile
language English
topic Vitrification
Fertility preservation
Cryopreservation
In Vitro Maturation
Ultrastructure
spellingShingle Vitrification
Fertility preservation
Cryopreservation
In Vitro Maturation
Ultrastructure
Izadi,Maryam
Eftekhar-Vaghefi,Seyed Hassan
Akbari,Hakimeh
Asadi-Shekari,Majid
Mokhtari,Tahmineh
Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro Maturation
description SUMMARY: Vitrification is a physical process in which the concentrated cryoprotectant solution after exposure to extreme cold without ice crystal formation in living cells to be converted glassing state. In this study, maturation rate and ultrastructure of mouse oocytes followed by vitrification before or after in-virto maturation (IVM) were evaluated. A total of 373 germinal vesicle oocytes were obtained from ovaries and divided into three fresh IVM, IVM vitrified, vitrified IVM groups. Ten metaphase II oocytes were obtained from uterine tubes and considered as the control group. Oocytes in vitrified groups were vitrified by Cryotop using vitrification medium and kept in liquid nitrogen. The maturation media was a-MEM supplemented with rFSH + hCG. After 24-48 h of incubation, the oocytes were investigated for nuclear maturation and ultrastructural changes using transmission electron microscopy (TEM). The oocyte maturation rate in vIVM group was significantly lower than IVMv group, when the two groups were compared with vIVM had the highest maturity. The evaluation ultrastructure of the four groups showed that the number of cortical granules, microvilli and mitochondria-SER aggregates in vIVM group were lowest and the highest amongst the number of vacuoles. Zona pellucida was darker than the control group in two freeze groups vIVM and IVMv. Most similar groups to the control group were group vIVM, Group IVMv and ultimately vIVM group, respectively. According to the results, IVM procedure is more efficient when it is performed before oocyte vitrification.
author Izadi,Maryam
Eftekhar-Vaghefi,Seyed Hassan
Akbari,Hakimeh
Asadi-Shekari,Majid
Mokhtari,Tahmineh
author_facet Izadi,Maryam
Eftekhar-Vaghefi,Seyed Hassan
Akbari,Hakimeh
Asadi-Shekari,Majid
Mokhtari,Tahmineh
author_sort Izadi,Maryam
title Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro Maturation
title_short Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro Maturation
title_full Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro Maturation
title_fullStr Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro Maturation
title_full_unstemmed Assessment of Mouse Oocytes Ultrastructure Following Vitrification Before and After in vitro Maturation
title_sort assessment of mouse oocytes ultrastructure following vitrification before and after in vitro maturation
publisher Sociedad Chilena de Anatomía
publishDate 2018
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022018000100180
work_keys_str_mv AT izadimaryam assessmentofmouseoocytesultrastructurefollowingvitrificationbeforeandafterinvitromaturation
AT eftekharvaghefiseyedhassan assessmentofmouseoocytesultrastructurefollowingvitrificationbeforeandafterinvitromaturation
AT akbarihakimeh assessmentofmouseoocytesultrastructurefollowingvitrificationbeforeandafterinvitromaturation
AT asadishekarimajid assessmentofmouseoocytesultrastructurefollowingvitrificationbeforeandafterinvitromaturation
AT mokhtaritahmineh assessmentofmouseoocytesultrastructurefollowingvitrificationbeforeandafterinvitromaturation
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