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Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro
Circulating angiogenic cells (CAC) influence vascular repair through the secretion of proangiogenic factors and cytokines. While CAC are deficient in patients with diabetes and exercise has a beneficial effect on CACs, the impact of these factors on paracrine secretion from CAC is unknown. We aimed...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758925/ https://www.ncbi.nlm.nih.gov/pubmed/26847726 http://dx.doi.org/10.14814/phy2.12649 |
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author | Witkowski, Sarah Guhanarayan, Gayatri Burgess, Rachel |
author_facet | Witkowski, Sarah Guhanarayan, Gayatri Burgess, Rachel |
author_sort | Witkowski, Sarah |
collection | PubMed |
description | Circulating angiogenic cells (CAC) influence vascular repair through the secretion of proangiogenic factors and cytokines. While CAC are deficient in patients with diabetes and exercise has a beneficial effect on CACs, the impact of these factors on paracrine secretion from CAC is unknown. We aimed to determine whether the in vitro secretion of selected cytokines and nitric oxide (NO) from CAC is influenced by hyperglycemia and acute exercise. Colony‐forming unit CAC (CFU‐CAC) were cultured from young active men (n = 9, 24 ± 2 years) at rest and after exercise under normal (5 mmol/L) and elevated (15 mmol/L) glucose. Preliminary relative multiplex cytokine analysis revealed that CAC conditioned culture media contained three of six measured cytokines: transforming growth factor‐beta‐1 (TGF β1), tumor necrosis factor alpha (TNF α), and monocyte chemotactic protein‐1 (MCP‐1). Single quantitative cytokine analysis was used to determine the concentration of each cytokine from the four conditions. NO was measured via Griess assay. There was a significant effect of CAC exposure to in vivo exercise on in vitro TGF β1 secretion (P = 0.024) that was independent of glucose concentration. There was no effect of glucose or acute exercise on TNF α or MCP‐1 concentration (both P > 0.05). The concentration of NO from CFU‐CAC cultured in elevated glucose was lower following acute exercise (P = 0.002) suggesting that exercise did not maintain NO secretion under hyperglycemic conditions. Our results identify paracrine signaling factors that may be responsible for the proangiogenic function of CFU‐CAC and an influence of acute exercise and elevated glucose on CFU‐CAC soluble factor secretion. |
format | Online Article Text |
id | pubmed-4758925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47589252016-02-29 Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro Witkowski, Sarah Guhanarayan, Gayatri Burgess, Rachel Physiol Rep Original Research Circulating angiogenic cells (CAC) influence vascular repair through the secretion of proangiogenic factors and cytokines. While CAC are deficient in patients with diabetes and exercise has a beneficial effect on CACs, the impact of these factors on paracrine secretion from CAC is unknown. We aimed to determine whether the in vitro secretion of selected cytokines and nitric oxide (NO) from CAC is influenced by hyperglycemia and acute exercise. Colony‐forming unit CAC (CFU‐CAC) were cultured from young active men (n = 9, 24 ± 2 years) at rest and after exercise under normal (5 mmol/L) and elevated (15 mmol/L) glucose. Preliminary relative multiplex cytokine analysis revealed that CAC conditioned culture media contained three of six measured cytokines: transforming growth factor‐beta‐1 (TGF β1), tumor necrosis factor alpha (TNF α), and monocyte chemotactic protein‐1 (MCP‐1). Single quantitative cytokine analysis was used to determine the concentration of each cytokine from the four conditions. NO was measured via Griess assay. There was a significant effect of CAC exposure to in vivo exercise on in vitro TGF β1 secretion (P = 0.024) that was independent of glucose concentration. There was no effect of glucose or acute exercise on TNF α or MCP‐1 concentration (both P > 0.05). The concentration of NO from CFU‐CAC cultured in elevated glucose was lower following acute exercise (P = 0.002) suggesting that exercise did not maintain NO secretion under hyperglycemic conditions. Our results identify paracrine signaling factors that may be responsible for the proangiogenic function of CFU‐CAC and an influence of acute exercise and elevated glucose on CFU‐CAC soluble factor secretion. John Wiley and Sons Inc. 2016-02-04 /pmc/articles/PMC4758925/ /pubmed/26847726 http://dx.doi.org/10.14814/phy2.12649 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Witkowski, Sarah Guhanarayan, Gayatri Burgess, Rachel Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro |
title | Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro |
title_full | Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro |
title_fullStr | Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro |
title_full_unstemmed | Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro |
title_short | Glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro |
title_sort | glucose and acute exercise influence factors secreted by circulating angiogenic cells in vitro |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758925/ https://www.ncbi.nlm.nih.gov/pubmed/26847726 http://dx.doi.org/10.14814/phy2.12649 |
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