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Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities
Blood oxygen saturation (SaO(2)) is one of the most important environmental factors in clinical heart protection. This study used human heart samples and human induced pluripotent stem cell−cardiomyocytes (iPSC-CMs) to assess how SaO(2) affects human CM cell cycle activities. The results showed that...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251192/ https://www.ncbi.nlm.nih.gov/pubmed/32478207 http://dx.doi.org/10.1016/j.jacbts.2020.02.008 |
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author | Ye, Lincai Qiu, Lisheng Feng, Bei Jiang, Chuan Huang, Yanhui Zhang, Haibo Zhang, Hao Hong, Haifa Liu, Jinfen |
author_facet | Ye, Lincai Qiu, Lisheng Feng, Bei Jiang, Chuan Huang, Yanhui Zhang, Haibo Zhang, Hao Hong, Haifa Liu, Jinfen |
author_sort | Ye, Lincai |
collection | PubMed |
description | Blood oxygen saturation (SaO(2)) is one of the most important environmental factors in clinical heart protection. This study used human heart samples and human induced pluripotent stem cell−cardiomyocytes (iPSC-CMs) to assess how SaO(2) affects human CM cell cycle activities. The results showed that there were significantly more cell cycle markers in the moderate hypoxia group (SaO(2): 75% to 85%) than in the other 2 groups (SaO(2) <75% or >85%). In iPSC-CMs 15% and 10% oxygen (O(2)) treatment increased cell cycle markers, whereas 5% and rapid change of O(2) decreased the markers. Moderate hypoxia is beneficial to the cell cycle activities of post-natal human CMs. |
format | Online Article Text |
id | pubmed-7251192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-72511922020-05-29 Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities Ye, Lincai Qiu, Lisheng Feng, Bei Jiang, Chuan Huang, Yanhui Zhang, Haibo Zhang, Hao Hong, Haifa Liu, Jinfen JACC Basic Transl Sci PRECLINICAL RESEARCH Blood oxygen saturation (SaO(2)) is one of the most important environmental factors in clinical heart protection. This study used human heart samples and human induced pluripotent stem cell−cardiomyocytes (iPSC-CMs) to assess how SaO(2) affects human CM cell cycle activities. The results showed that there were significantly more cell cycle markers in the moderate hypoxia group (SaO(2): 75% to 85%) than in the other 2 groups (SaO(2) <75% or >85%). In iPSC-CMs 15% and 10% oxygen (O(2)) treatment increased cell cycle markers, whereas 5% and rapid change of O(2) decreased the markers. Moderate hypoxia is beneficial to the cell cycle activities of post-natal human CMs. Elsevier 2020-04-22 /pmc/articles/PMC7251192/ /pubmed/32478207 http://dx.doi.org/10.1016/j.jacbts.2020.02.008 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | PRECLINICAL RESEARCH Ye, Lincai Qiu, Lisheng Feng, Bei Jiang, Chuan Huang, Yanhui Zhang, Haibo Zhang, Hao Hong, Haifa Liu, Jinfen Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities |
title | Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities |
title_full | Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities |
title_fullStr | Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities |
title_full_unstemmed | Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities |
title_short | Role of Blood Oxygen Saturation During Post-Natal Human Cardiomyocyte Cell Cycle Activities |
title_sort | role of blood oxygen saturation during post-natal human cardiomyocyte cell cycle activities |
topic | PRECLINICAL RESEARCH |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251192/ https://www.ncbi.nlm.nih.gov/pubmed/32478207 http://dx.doi.org/10.1016/j.jacbts.2020.02.008 |
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