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Endometrial regenerative cells: A novel stem cell population
Angiogenesis is a critical component of the proliferative endometrial phase of the menstrual cycle. Thus, we hypothesized that a stem cell-like population exist and can be isolated from menstrual blood. Mononuclear cells collected from the menstrual blood contained a subpopulation of adherent cells...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212625/ https://www.ncbi.nlm.nih.gov/pubmed/18005405 http://dx.doi.org/10.1186/1479-5876-5-57 |
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author | Meng, Xiaolong Ichim, Thomas E Zhong, Jie Rogers, Andrea Yin, Zhenglian Jackson, James Wang, Hao Ge, Wei Bogin, Vladimir Chan, Kyle W Thébaud, Bernard Riordan, Neil H |
author_facet | Meng, Xiaolong Ichim, Thomas E Zhong, Jie Rogers, Andrea Yin, Zhenglian Jackson, James Wang, Hao Ge, Wei Bogin, Vladimir Chan, Kyle W Thébaud, Bernard Riordan, Neil H |
author_sort | Meng, Xiaolong |
collection | PubMed |
description | Angiogenesis is a critical component of the proliferative endometrial phase of the menstrual cycle. Thus, we hypothesized that a stem cell-like population exist and can be isolated from menstrual blood. Mononuclear cells collected from the menstrual blood contained a subpopulation of adherent cells which could be maintained in tissue culture for >68 doublings and retained expression of the markers CD9, CD29, CD41a, CD44, CD59, CD73, CD90 and CD105, without karyotypic abnormalities. Proliferative rate of the cells was significantly higher than control umbilical cord derived mesenchymal stem cells, with doubling occurring every 19.4 hours. These cells, which we termed "Endometrial Regenerative Cells" (ERC) were capable of differentiating into 9 lineages: cardiomyocytic, respiratory epithelial, neurocytic, myocytic, endothelial, pancreatic, hepatic, adipocytic, and osteogenic. Additionally, ERC produced MMP3, MMP10, GM-CSF, angiopoietin-2 and PDGF-BB at 10–100,000 fold higher levels than two control cord blood derived mesenchymal stem cell lines. Given the ease of extraction and pluripotency of this cell population, we propose ERC as a novel alternative to current stem cells sources. |
format | Text |
id | pubmed-2212625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22126252008-01-24 Endometrial regenerative cells: A novel stem cell population Meng, Xiaolong Ichim, Thomas E Zhong, Jie Rogers, Andrea Yin, Zhenglian Jackson, James Wang, Hao Ge, Wei Bogin, Vladimir Chan, Kyle W Thébaud, Bernard Riordan, Neil H J Transl Med Research Angiogenesis is a critical component of the proliferative endometrial phase of the menstrual cycle. Thus, we hypothesized that a stem cell-like population exist and can be isolated from menstrual blood. Mononuclear cells collected from the menstrual blood contained a subpopulation of adherent cells which could be maintained in tissue culture for >68 doublings and retained expression of the markers CD9, CD29, CD41a, CD44, CD59, CD73, CD90 and CD105, without karyotypic abnormalities. Proliferative rate of the cells was significantly higher than control umbilical cord derived mesenchymal stem cells, with doubling occurring every 19.4 hours. These cells, which we termed "Endometrial Regenerative Cells" (ERC) were capable of differentiating into 9 lineages: cardiomyocytic, respiratory epithelial, neurocytic, myocytic, endothelial, pancreatic, hepatic, adipocytic, and osteogenic. Additionally, ERC produced MMP3, MMP10, GM-CSF, angiopoietin-2 and PDGF-BB at 10–100,000 fold higher levels than two control cord blood derived mesenchymal stem cell lines. Given the ease of extraction and pluripotency of this cell population, we propose ERC as a novel alternative to current stem cells sources. BioMed Central 2007-11-15 /pmc/articles/PMC2212625/ /pubmed/18005405 http://dx.doi.org/10.1186/1479-5876-5-57 Text en Copyright © 2007 Meng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Meng, Xiaolong Ichim, Thomas E Zhong, Jie Rogers, Andrea Yin, Zhenglian Jackson, James Wang, Hao Ge, Wei Bogin, Vladimir Chan, Kyle W Thébaud, Bernard Riordan, Neil H Endometrial regenerative cells: A novel stem cell population |
title | Endometrial regenerative cells: A novel stem cell population |
title_full | Endometrial regenerative cells: A novel stem cell population |
title_fullStr | Endometrial regenerative cells: A novel stem cell population |
title_full_unstemmed | Endometrial regenerative cells: A novel stem cell population |
title_short | Endometrial regenerative cells: A novel stem cell population |
title_sort | endometrial regenerative cells: a novel stem cell population |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212625/ https://www.ncbi.nlm.nih.gov/pubmed/18005405 http://dx.doi.org/10.1186/1479-5876-5-57 |
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