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In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst
Profiling transcriptome at single cell level of bovine blastocysts derived in vivo (IVV), in vitro from conventional culture medium (IVC), and reduced nutrient culture medium (IVR) has enabled us to reveal cell lineage segregation, during which forming inner cell mass (ICM), trophectoderm (TE), and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274902/ https://www.ncbi.nlm.nih.gov/pubmed/37333292 http://dx.doi.org/10.1101/2023.06.09.544379 |
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author | Ming, Hao Zhang, Mingxiang Rajput, Sandeep Logsdon, Deirdre Zhu, Linkai Schoolcraft, William B Krisher, Rebecca Jiang, Zongliang Yuan, Ye |
author_facet | Ming, Hao Zhang, Mingxiang Rajput, Sandeep Logsdon, Deirdre Zhu, Linkai Schoolcraft, William B Krisher, Rebecca Jiang, Zongliang Yuan, Ye |
author_sort | Ming, Hao |
collection | PubMed |
description | Profiling transcriptome at single cell level of bovine blastocysts derived in vivo (IVV), in vitro from conventional culture medium (IVC), and reduced nutrient culture medium (IVR) has enabled us to reveal cell lineage segregation, during which forming inner cell mass (ICM), trophectoderm (TE), and an undefined population of transitional cells. Only IVV embryos had well-defined ICM, indicating in vitro culture may delay the first cell fate commitment to ICM. Differences between IVV, IVC and IVR embryos were mainly contributed by ICM and transitional cells. Pathway analysis by using the differentially expressed genes of these non-TE cells between groups pointed to highly active metabolic and biosynthetic processes, with reduced cellular signaling and membrane transport in IVC embryos, which may lead to reduced developmental potential. IVR embryos had lower activities in metabolic and biosynthetic processes, but increased cellular signaling and membrane transport, suggesting these cellular mechanisms may contribute to the improved blastocyst development compared to IVC embryos. However, the IVR embryos had compromised development when compared to IVV embryos with notably over-active membrane transport activities that led to impaired ion homeostasis. |
format | Online Article Text |
id | pubmed-10274902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-102749022023-06-17 In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst Ming, Hao Zhang, Mingxiang Rajput, Sandeep Logsdon, Deirdre Zhu, Linkai Schoolcraft, William B Krisher, Rebecca Jiang, Zongliang Yuan, Ye bioRxiv Article Profiling transcriptome at single cell level of bovine blastocysts derived in vivo (IVV), in vitro from conventional culture medium (IVC), and reduced nutrient culture medium (IVR) has enabled us to reveal cell lineage segregation, during which forming inner cell mass (ICM), trophectoderm (TE), and an undefined population of transitional cells. Only IVV embryos had well-defined ICM, indicating in vitro culture may delay the first cell fate commitment to ICM. Differences between IVV, IVC and IVR embryos were mainly contributed by ICM and transitional cells. Pathway analysis by using the differentially expressed genes of these non-TE cells between groups pointed to highly active metabolic and biosynthetic processes, with reduced cellular signaling and membrane transport in IVC embryos, which may lead to reduced developmental potential. IVR embryos had lower activities in metabolic and biosynthetic processes, but increased cellular signaling and membrane transport, suggesting these cellular mechanisms may contribute to the improved blastocyst development compared to IVC embryos. However, the IVR embryos had compromised development when compared to IVV embryos with notably over-active membrane transport activities that led to impaired ion homeostasis. Cold Spring Harbor Laboratory 2023-06-11 /pmc/articles/PMC10274902/ /pubmed/37333292 http://dx.doi.org/10.1101/2023.06.09.544379 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Ming, Hao Zhang, Mingxiang Rajput, Sandeep Logsdon, Deirdre Zhu, Linkai Schoolcraft, William B Krisher, Rebecca Jiang, Zongliang Yuan, Ye In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst |
title | In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst |
title_full | In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst |
title_fullStr | In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst |
title_full_unstemmed | In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst |
title_short | In Vitro Culture Alters Cell Lineage Composition and Cellular Metabolism of Bovine Blastocyst |
title_sort | in vitro culture alters cell lineage composition and cellular metabolism of bovine blastocyst |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274902/ https://www.ncbi.nlm.nih.gov/pubmed/37333292 http://dx.doi.org/10.1101/2023.06.09.544379 |
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