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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Main Authors: Dongqiang Song, Yuanmin Li, Jiatian Cao, Zhihua Han, Lin Gao, Zuojun Xu, Zhaofang Yin, Guifang Wang, Yuqi Fan, Changqian Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23762416/?tool=EBI
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spelling 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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