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Human exhaled air can efficiently support in vitro maturation of porcine oocytes and subsequent early embryonic development
Air phase is an indispensable environmental factor affecting oocyte maturation and early embryo development. Human exhaled air was previously proved to be a reliable and inexpensive atmosphere that sustains normal early development of mouse and bovine embryos. However, whether human exhaled air can...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Colégio Brasileiro de Reprodução Animal
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746221/ https://www.ncbi.nlm.nih.gov/pubmed/33365092 http://dx.doi.org/10.21451/1984-3143-AR2017-0027 |
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author | Cao, Zubing Gao, Di Xu, Tengteng Tong, Xu Wang, Yiqing Li, Yunsheng Fang, Fugui Ding, Jianping Zhang, Xiaorong Zhang, Yunhai |
author_facet | Cao, Zubing Gao, Di Xu, Tengteng Tong, Xu Wang, Yiqing Li, Yunsheng Fang, Fugui Ding, Jianping Zhang, Xiaorong Zhang, Yunhai |
author_sort | Cao, Zubing |
collection | PubMed |
description | Air phase is an indispensable environmental factor affecting oocyte maturation and early embryo development. Human exhaled air was previously proved to be a reliable and inexpensive atmosphere that sustains normal early development of mouse and bovine embryos. However, whether human exhaled air can support in vitro maturation (IVM) of porcine oocytes is not yet known. To evaluate the feasibility of maturing oocytes in human exhaled air, we examined oocyte morphology, BMP15 expression, nuclear and cytoplasmic maturation. We found that cumulus expansion status, expression levels of BMP15 important for cumulus expansion and the rate of first polar body emission were similar among human exhaled air, 5% O(2) or 20% O(2) in air after IVM of 44 h. Furthermore, the percentage of metaphase II (MII) oocytes showing normal cortical and sub-membranous localization of cortical granules and diffused mitochondrial distribution patterns is comparable among groups. The cleavage, blastocyst rate and total cell number were not apparently different for parthenogenetic activated and somatic cloned embryos derived from MII oocytes matured in three air phases, suggesting oocytes matured in human exhaled air obtain normal developmental competence. Taken together, human exhaled air can efficiently support in vitro maturation of porcine oocytes and subsequent early embryonic development. |
format | Online Article Text |
id | pubmed-7746221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Colégio Brasileiro de Reprodução Animal |
record_format | MEDLINE/PubMed |
spelling | pubmed-77462212020-12-22 Human exhaled air can efficiently support in vitro maturation of porcine oocytes and subsequent early embryonic development Cao, Zubing Gao, Di Xu, Tengteng Tong, Xu Wang, Yiqing Li, Yunsheng Fang, Fugui Ding, Jianping Zhang, Xiaorong Zhang, Yunhai Anim Reprod Original Article Air phase is an indispensable environmental factor affecting oocyte maturation and early embryo development. Human exhaled air was previously proved to be a reliable and inexpensive atmosphere that sustains normal early development of mouse and bovine embryos. However, whether human exhaled air can support in vitro maturation (IVM) of porcine oocytes is not yet known. To evaluate the feasibility of maturing oocytes in human exhaled air, we examined oocyte morphology, BMP15 expression, nuclear and cytoplasmic maturation. We found that cumulus expansion status, expression levels of BMP15 important for cumulus expansion and the rate of first polar body emission were similar among human exhaled air, 5% O(2) or 20% O(2) in air after IVM of 44 h. Furthermore, the percentage of metaphase II (MII) oocytes showing normal cortical and sub-membranous localization of cortical granules and diffused mitochondrial distribution patterns is comparable among groups. The cleavage, blastocyst rate and total cell number were not apparently different for parthenogenetic activated and somatic cloned embryos derived from MII oocytes matured in three air phases, suggesting oocytes matured in human exhaled air obtain normal developmental competence. Taken together, human exhaled air can efficiently support in vitro maturation of porcine oocytes and subsequent early embryonic development. Colégio Brasileiro de Reprodução Animal 2018-08-16 /pmc/articles/PMC7746221/ /pubmed/33365092 http://dx.doi.org/10.21451/1984-3143-AR2017-0027 Text en http://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. |
spellingShingle | Original Article Cao, Zubing Gao, Di Xu, Tengteng Tong, Xu Wang, Yiqing Li, Yunsheng Fang, Fugui Ding, Jianping Zhang, Xiaorong Zhang, Yunhai Human exhaled air can efficiently support in vitro maturation of porcine oocytes and subsequent early embryonic development |
title |
Human exhaled air can efficiently support in vitro maturation of porcine
oocytes and subsequent early embryonic development
|
title_full |
Human exhaled air can efficiently support in vitro maturation of porcine
oocytes and subsequent early embryonic development
|
title_fullStr |
Human exhaled air can efficiently support in vitro maturation of porcine
oocytes and subsequent early embryonic development
|
title_full_unstemmed |
Human exhaled air can efficiently support in vitro maturation of porcine
oocytes and subsequent early embryonic development
|
title_short |
Human exhaled air can efficiently support in vitro maturation of porcine
oocytes and subsequent early embryonic development
|
title_sort | human exhaled air can efficiently support in vitro maturation of porcine
oocytes and subsequent early embryonic development |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746221/ https://www.ncbi.nlm.nih.gov/pubmed/33365092 http://dx.doi.org/10.21451/1984-3143-AR2017-0027 |
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