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Establishment of bovine embryonic stem cells after knockdown of CDX2

Bovine embryonic stem cells (bESCs) have not been successfully established yet. One reason could be that CDX2, as the trophectoderm regulator, expresses in bovine inner cell mass (ICM), which probably becomes a technical barrier for maintaining the pluripotency of bESCs in vitro. We hypothesized tha...

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Autores principales: Wu, Xia, Song, Miao, Yang, Xi, Liu, Xin, Liu, Kun, Jiao, Cuihua, Wang, Jinze, Bai, Chunling, Su, Guanghua, Liu, Xuefei, Li, Guangpeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913270/
https://www.ncbi.nlm.nih.gov/pubmed/27320776
http://dx.doi.org/10.1038/srep28343
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author Wu, Xia
Song, Miao
Yang, Xi
Liu, Xin
Liu, Kun
Jiao, Cuihua
Wang, Jinze
Bai, Chunling
Su, Guanghua
Liu, Xuefei
Li, Guangpeng
author_facet Wu, Xia
Song, Miao
Yang, Xi
Liu, Xin
Liu, Kun
Jiao, Cuihua
Wang, Jinze
Bai, Chunling
Su, Guanghua
Liu, Xuefei
Li, Guangpeng
author_sort Wu, Xia
collection PubMed
description Bovine embryonic stem cells (bESCs) have not been successfully established yet. One reason could be that CDX2, as the trophectoderm regulator, expresses in bovine inner cell mass (ICM), which probably becomes a technical barrier for maintaining the pluripotency of bESCs in vitro. We hypothesized that CDX2 knockdown (CDX2-KD) could remove such negative effort, which will be helpful for capturing complete and permanent capacity of pluripotency. Expression and localization of pluripotent genes were not affected in CDX2-KD blastocysts. The CDX2-KD bESCs grew into monolayers on feeder layer. Pluripotent genes expressed at an improved levels and lasted longer time in CDX2-KD bESCs, along with down-regulation of DNA methylation on promoters of both OCT4 and SOX2. The cystic structure typical for trophoblast cells did not show during culturing CDX2-KD bESCs. CDX2-KD bESC-derived Embryoid bodies showed with compact morphology and with the improved levels of differentiations in three germ layers. CDX2-KD bESCs still carried the capacity of forming teratomas with three germ layers after long-term culture. In summary, CDX2 in bovine ICM was inducer of trophoblast lineage with negative effect on maintenance of pluripotency of bESCs. Precise regulation CDX2 expression to switch on/off will be studied next for application on establishment of bESCs.
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spelling pubmed-49132702016-06-21 Establishment of bovine embryonic stem cells after knockdown of CDX2 Wu, Xia Song, Miao Yang, Xi Liu, Xin Liu, Kun Jiao, Cuihua Wang, Jinze Bai, Chunling Su, Guanghua Liu, Xuefei Li, Guangpeng Sci Rep Article Bovine embryonic stem cells (bESCs) have not been successfully established yet. One reason could be that CDX2, as the trophectoderm regulator, expresses in bovine inner cell mass (ICM), which probably becomes a technical barrier for maintaining the pluripotency of bESCs in vitro. We hypothesized that CDX2 knockdown (CDX2-KD) could remove such negative effort, which will be helpful for capturing complete and permanent capacity of pluripotency. Expression and localization of pluripotent genes were not affected in CDX2-KD blastocysts. The CDX2-KD bESCs grew into monolayers on feeder layer. Pluripotent genes expressed at an improved levels and lasted longer time in CDX2-KD bESCs, along with down-regulation of DNA methylation on promoters of both OCT4 and SOX2. The cystic structure typical for trophoblast cells did not show during culturing CDX2-KD bESCs. CDX2-KD bESC-derived Embryoid bodies showed with compact morphology and with the improved levels of differentiations in three germ layers. CDX2-KD bESCs still carried the capacity of forming teratomas with three germ layers after long-term culture. In summary, CDX2 in bovine ICM was inducer of trophoblast lineage with negative effect on maintenance of pluripotency of bESCs. Precise regulation CDX2 expression to switch on/off will be studied next for application on establishment of bESCs. Nature Publishing Group 2016-06-20 /pmc/articles/PMC4913270/ /pubmed/27320776 http://dx.doi.org/10.1038/srep28343 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wu, Xia
Song, Miao
Yang, Xi
Liu, Xin
Liu, Kun
Jiao, Cuihua
Wang, Jinze
Bai, Chunling
Su, Guanghua
Liu, Xuefei
Li, Guangpeng
Establishment of bovine embryonic stem cells after knockdown of CDX2
title Establishment of bovine embryonic stem cells after knockdown of CDX2
title_full Establishment of bovine embryonic stem cells after knockdown of CDX2
title_fullStr Establishment of bovine embryonic stem cells after knockdown of CDX2
title_full_unstemmed Establishment of bovine embryonic stem cells after knockdown of CDX2
title_short Establishment of bovine embryonic stem cells after knockdown of CDX2
title_sort establishment of bovine embryonic stem cells after knockdown of cdx2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913270/
https://www.ncbi.nlm.nih.gov/pubmed/27320776
http://dx.doi.org/10.1038/srep28343
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