Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro.
<h4>Aim</h4>Iron deficiency is a common comorbidity in chronic heart failure (CHF) which may exacerbate CHF. The c-kit⁺ cardiac stem cells (CSCs) play a vital role in cardiac function repair. However, much is unknown regarding the role of iron deficiency in regulating c-kit⁺ CSCs functio...
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doaj-f10dcc92ed8a4158931bbc527e330f3d2021-03-03T23:16:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0186e6572110.1371/journal.pone.0065721Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro.Dongqiang SongYuanmin LiJiatian CaoZhihua HanLin GaoZuojun XuZhaofang YinGuifang WangYuqi FanChangqian Wang<h4>Aim</h4>Iron deficiency is a common comorbidity in chronic heart failure (CHF) which may exacerbate CHF. The c-kit⁺ cardiac stem cells (CSCs) play a vital role in cardiac function repair. However, much is unknown regarding the role of iron deficiency in regulating c-kit⁺ CSCs function. In this study, we investigated whether iron deficiency regulates c-kit⁺ CSCs proliferation, migration, apoptosis, and differentiation in vitro.<h4>Method</h4>All c-kit⁺ CSCs were isolated from adult C57BL/6 mice. The c-kit⁺ CSCs were cultured with deferoxamine (DFO, an iron chelator), mimosine (MIM, another iron chelator), or a complex of DFO and iron (Fe(III)), respectively. Cell migration was assayed using a 48-well chamber system. Proliferation, cell cycle, and apoptosis of c-kit⁺ CSCs were analyzed with BrdU labeling, population doubling time assay, CCK-8 assay, and flow cytometry. Caspase-3 protein level and activity were examined with Western blotting and spectrophotometric detection. The changes in the expression of cardiac-specific proteins (GATA-4,TNI, and β-MHC) and cell cycle-related proteins (cyclin D1, RB, and pRB) were detected with Western blotting.<h4>Result</h4>DFO and MIM suppressed c-kit⁺ CSCs proliferation and differentiation. They also modulated cell cycle and cardiac-specific protein expression. Iron chelators down-regulated the expression and phosphorylation of cell cycle-related proteins. Iron reversed those suppressive effects of DFO. DFO and MIM didn't affect c-kit⁺ CSCs migration and apoptosis.<h4>Conclusion</h4>Iron deficiency suppressed proliferation and differentiation of c-kit⁺ CSCs. This may partly explain how iron deficiency affects CHF prognosis.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23762416/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dongqiang Song Yuanmin Li Jiatian Cao Zhihua Han Lin Gao Zuojun Xu Zhaofang Yin Guifang Wang Yuqi Fan Changqian Wang |
spellingShingle |
Dongqiang Song Yuanmin Li Jiatian Cao Zhihua Han Lin Gao Zuojun Xu Zhaofang Yin Guifang Wang Yuqi Fan Changqian Wang Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro. PLoS ONE |
author_facet |
Dongqiang Song Yuanmin Li Jiatian Cao Zhihua Han Lin Gao Zuojun Xu Zhaofang Yin Guifang Wang Yuqi Fan Changqian Wang |
author_sort |
Dongqiang Song |
title |
Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro. |
title_short |
Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro. |
title_full |
Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro. |
title_fullStr |
Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro. |
title_full_unstemmed |
Effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro. |
title_sort |
effect of iron deficiency on c-kit⁺ cardiac stem cells in vitro. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
<h4>Aim</h4>Iron deficiency is a common comorbidity in chronic heart failure (CHF) which may exacerbate CHF. The c-kit⁺ cardiac stem cells (CSCs) play a vital role in cardiac function repair. However, much is unknown regarding the role of iron deficiency in regulating c-kit⁺ CSCs function. In this study, we investigated whether iron deficiency regulates c-kit⁺ CSCs proliferation, migration, apoptosis, and differentiation in vitro.<h4>Method</h4>All c-kit⁺ CSCs were isolated from adult C57BL/6 mice. The c-kit⁺ CSCs were cultured with deferoxamine (DFO, an iron chelator), mimosine (MIM, another iron chelator), or a complex of DFO and iron (Fe(III)), respectively. Cell migration was assayed using a 48-well chamber system. Proliferation, cell cycle, and apoptosis of c-kit⁺ CSCs were analyzed with BrdU labeling, population doubling time assay, CCK-8 assay, and flow cytometry. Caspase-3 protein level and activity were examined with Western blotting and spectrophotometric detection. The changes in the expression of cardiac-specific proteins (GATA-4,TNI, and β-MHC) and cell cycle-related proteins (cyclin D1, RB, and pRB) were detected with Western blotting.<h4>Result</h4>DFO and MIM suppressed c-kit⁺ CSCs proliferation and differentiation. They also modulated cell cycle and cardiac-specific protein expression. Iron chelators down-regulated the expression and phosphorylation of cell cycle-related proteins. Iron reversed those suppressive effects of DFO. DFO and MIM didn't affect c-kit⁺ CSCs migration and apoptosis.<h4>Conclusion</h4>Iron deficiency suppressed proliferation and differentiation of c-kit⁺ CSCs. This may partly explain how iron deficiency affects CHF prognosis. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23762416/?tool=EBI |
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