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Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential

Endothelial progenitor cell (EPC) transplantation is beneficial for ischemic diseases such as critical limb ischemia and ischemic heart disease. The scarcity of functional EPCs in adults is a limiting factor for EPC transplantation therapy. The quality and quantity culture (QQc) system is an effecti...

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Autores principales: Hagiwara, Hiroko, Higashibata, Akira, Ogawa, Shiho, Kanazawa, Shigeyuki, Mizuno, Hiroshi, Tanaka, Rica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155294/
https://www.ncbi.nlm.nih.gov/pubmed/30250055
http://dx.doi.org/10.1038/s41598-018-32073-2
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author Hagiwara, Hiroko
Higashibata, Akira
Ogawa, Shiho
Kanazawa, Shigeyuki
Mizuno, Hiroshi
Tanaka, Rica
author_facet Hagiwara, Hiroko
Higashibata, Akira
Ogawa, Shiho
Kanazawa, Shigeyuki
Mizuno, Hiroshi
Tanaka, Rica
author_sort Hagiwara, Hiroko
collection PubMed
description Endothelial progenitor cell (EPC) transplantation is beneficial for ischemic diseases such as critical limb ischemia and ischemic heart disease. The scarcity of functional EPCs in adults is a limiting factor for EPC transplantation therapy. The quality and quantity culture (QQc) system is an effective ex vivo method for enhancing the number and angiogenic potential of EPCs. Further, microgravity environments have been shown to enhance the functional potential of stem cells. We therefore hypothesized that cells cultured with QQc under microgravity may have enhanced functionality. We cultured human peripheral blood mononuclear cells using QQc under normal (E), microgravity (MG), or microgravity followed by normal (ME) conditions and found that ME resulted in the most significant increase in CD34+ and double positive Dil-Ac-LDL-FITC-Ulex-Lectin cells, both EPC markers. Furthermore, angiogenic potential was determined by an EPC-colony forming assay. While numbers of primitive EPC-colony forming units (pEPC-CFU) did not change, numbers of definitive EPC-CFU colonies increased most under ME conditions. Gene-expression profiling also identified increases in angiogenic factors, including vascular endothelial growth factor, under MG and ME conditions. Thus, QQc along with ME conditions could be an efficient system for significantly enhancing the number and angiogenic potential of EPCs.
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spelling pubmed-61552942018-09-28 Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential Hagiwara, Hiroko Higashibata, Akira Ogawa, Shiho Kanazawa, Shigeyuki Mizuno, Hiroshi Tanaka, Rica Sci Rep Article Endothelial progenitor cell (EPC) transplantation is beneficial for ischemic diseases such as critical limb ischemia and ischemic heart disease. The scarcity of functional EPCs in adults is a limiting factor for EPC transplantation therapy. The quality and quantity culture (QQc) system is an effective ex vivo method for enhancing the number and angiogenic potential of EPCs. Further, microgravity environments have been shown to enhance the functional potential of stem cells. We therefore hypothesized that cells cultured with QQc under microgravity may have enhanced functionality. We cultured human peripheral blood mononuclear cells using QQc under normal (E), microgravity (MG), or microgravity followed by normal (ME) conditions and found that ME resulted in the most significant increase in CD34+ and double positive Dil-Ac-LDL-FITC-Ulex-Lectin cells, both EPC markers. Furthermore, angiogenic potential was determined by an EPC-colony forming assay. While numbers of primitive EPC-colony forming units (pEPC-CFU) did not change, numbers of definitive EPC-CFU colonies increased most under ME conditions. Gene-expression profiling also identified increases in angiogenic factors, including vascular endothelial growth factor, under MG and ME conditions. Thus, QQc along with ME conditions could be an efficient system for significantly enhancing the number and angiogenic potential of EPCs. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155294/ /pubmed/30250055 http://dx.doi.org/10.1038/s41598-018-32073-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hagiwara, Hiroko
Higashibata, Akira
Ogawa, Shiho
Kanazawa, Shigeyuki
Mizuno, Hiroshi
Tanaka, Rica
Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential
title Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential
title_full Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential
title_fullStr Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential
title_full_unstemmed Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential
title_short Effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential
title_sort effectiveness of endothelial progenitor cell culture under microgravity for improved angiogenic potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155294/
https://www.ncbi.nlm.nih.gov/pubmed/30250055
http://dx.doi.org/10.1038/s41598-018-32073-2
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