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Characterization of vascular endothelial progenitor cells from chicken bone marrow
BACKGROUND: Endothelial progenitor cells (EPC) are a type of stem cell used in the treatment of atherosclerosis, vascular injury and regeneration. At present, most of the EPCs studied are from human and mouse, whereas the study of poultry-derived EPCs has rarely been reported. In the present study,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408357/ https://www.ncbi.nlm.nih.gov/pubmed/22584105 http://dx.doi.org/10.1186/1746-6148-8-54 |
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author | Bai, Chunyu Hou, Lingling Zhang, Minghai Pu, Yabin Guan, Weijun Ma, Yuehui |
author_facet | Bai, Chunyu Hou, Lingling Zhang, Minghai Pu, Yabin Guan, Weijun Ma, Yuehui |
author_sort | Bai, Chunyu |
collection | PubMed |
description | BACKGROUND: Endothelial progenitor cells (EPC) are a type of stem cell used in the treatment of atherosclerosis, vascular injury and regeneration. At present, most of the EPCs studied are from human and mouse, whereas the study of poultry-derived EPCs has rarely been reported. In the present study, chicken bone marrow-derived EPCs were isolated and studied at the cellular level using immunofluorescence and RT-PCR. RESULTS: We found that the majority of chicken EPCs were spindle shaped. The growth-curves of chicken EPCs at passages (P) 1, -5 and -9 were typically “S”-shaped. The viability of chicken EPCs, before and after cryopreservation was 92.2% and 81.1%, respectively. Thus, cryopreservation had no obvious effects on the viability of chicken EPCs. Dil-ac-LDL and FITC-UAE-1 uptake assays and immunofluorescent detection of the cell surface markers CD34, CD133, VEGFR-2 confirmed that the cells obtained in vitro were EPCs. Observation of endothelial-specific Weibel-Palade bodies using transmission electron microscopy further confirmed that the cells were of endothelial lineage. In addition, chicken EPCs differentiated into endothelial cells and smooth muscle cells upon induction with VEGF and PDGF-BB, respectively, suggesting that the chicken EPCs retained multipotency in vitro. CONCLUSIONS: These results suggest that chicken EPCs not only have strong self-renewal capacity, but also the potential to differentiate into endothelial and smooth muscle cells. This research provides theoretical basis and experimental evidence for potential therapeutic application of endothelial progenitor cells in the treatment of atherosclerosis, vascular injury and diabetic complications. |
format | Online Article Text |
id | pubmed-3408357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34083572012-07-31 Characterization of vascular endothelial progenitor cells from chicken bone marrow Bai, Chunyu Hou, Lingling Zhang, Minghai Pu, Yabin Guan, Weijun Ma, Yuehui BMC Vet Res Research Article BACKGROUND: Endothelial progenitor cells (EPC) are a type of stem cell used in the treatment of atherosclerosis, vascular injury and regeneration. At present, most of the EPCs studied are from human and mouse, whereas the study of poultry-derived EPCs has rarely been reported. In the present study, chicken bone marrow-derived EPCs were isolated and studied at the cellular level using immunofluorescence and RT-PCR. RESULTS: We found that the majority of chicken EPCs were spindle shaped. The growth-curves of chicken EPCs at passages (P) 1, -5 and -9 were typically “S”-shaped. The viability of chicken EPCs, before and after cryopreservation was 92.2% and 81.1%, respectively. Thus, cryopreservation had no obvious effects on the viability of chicken EPCs. Dil-ac-LDL and FITC-UAE-1 uptake assays and immunofluorescent detection of the cell surface markers CD34, CD133, VEGFR-2 confirmed that the cells obtained in vitro were EPCs. Observation of endothelial-specific Weibel-Palade bodies using transmission electron microscopy further confirmed that the cells were of endothelial lineage. In addition, chicken EPCs differentiated into endothelial cells and smooth muscle cells upon induction with VEGF and PDGF-BB, respectively, suggesting that the chicken EPCs retained multipotency in vitro. CONCLUSIONS: These results suggest that chicken EPCs not only have strong self-renewal capacity, but also the potential to differentiate into endothelial and smooth muscle cells. This research provides theoretical basis and experimental evidence for potential therapeutic application of endothelial progenitor cells in the treatment of atherosclerosis, vascular injury and diabetic complications. BioMed Central 2012-05-14 /pmc/articles/PMC3408357/ /pubmed/22584105 http://dx.doi.org/10.1186/1746-6148-8-54 Text en Copyright ©2012 Bai 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 Article Bai, Chunyu Hou, Lingling Zhang, Minghai Pu, Yabin Guan, Weijun Ma, Yuehui Characterization of vascular endothelial progenitor cells from chicken bone marrow |
title | Characterization of vascular endothelial progenitor cells from chicken bone marrow |
title_full | Characterization of vascular endothelial progenitor cells from chicken bone marrow |
title_fullStr | Characterization of vascular endothelial progenitor cells from chicken bone marrow |
title_full_unstemmed | Characterization of vascular endothelial progenitor cells from chicken bone marrow |
title_short | Characterization of vascular endothelial progenitor cells from chicken bone marrow |
title_sort | characterization of vascular endothelial progenitor cells from chicken bone marrow |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408357/ https://www.ncbi.nlm.nih.gov/pubmed/22584105 http://dx.doi.org/10.1186/1746-6148-8-54 |
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