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Over-expression of HO-1 on mesenchymal stem cells promotes angiogenesis and improves myocardial function in infarcted myocardium
by
Zhang, Yan
, Lin, Guosheng
, Zeng, Bin
, Ren, Xiaofeng
, Chen, Honglei
in
Animals
/ Apoptosis
/ Biomedical and Life Sciences
/ Biomedicine
/ Bone marrow
/ Enzymes
/ Fibroblast growth factors
/ Gene therapy
/ Growth factors
/ Heart attacks
/ Heme
/ Heme Oxygenase-1 - genetics
/ Heme Oxygenase-1 - metabolism
/ Hemodynamics
/ In Situ Nick-End Labeling
/ Male
/ Mesenchymal Stem Cell Transplantation
/ Mesenchymal Stromal Cells - metabolism
/ Myocardial infarction
/ Myocardial Infarction - metabolism
/ Myocardial Infarction - pathology
/ Myocardial Infarction - surgery
/ Myocardium - cytology
/ Myocardium - metabolism
/ Myocardium - pathology
/ Neovascularization, Physiologic
/ Proteins
/ Rats
/ Rats, Sprague-Dawley
/ Rodents
/ Stem cells
/ Vascular endothelial growth factor
/ Ventricular Remodeling
2010
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Over-expression of HO-1 on mesenchymal stem cells promotes angiogenesis and improves myocardial function in infarcted myocardium
by
Zhang, Yan
, Lin, Guosheng
, Zeng, Bin
, Ren, Xiaofeng
, Chen, Honglei
in
Animals
/ Apoptosis
/ Biomedical and Life Sciences
/ Biomedicine
/ Bone marrow
/ Enzymes
/ Fibroblast growth factors
/ Gene therapy
/ Growth factors
/ Heart attacks
/ Heme
/ Heme Oxygenase-1 - genetics
/ Heme Oxygenase-1 - metabolism
/ Hemodynamics
/ In Situ Nick-End Labeling
/ Male
/ Mesenchymal Stem Cell Transplantation
/ Mesenchymal Stromal Cells - metabolism
/ Myocardial infarction
/ Myocardial Infarction - metabolism
/ Myocardial Infarction - pathology
/ Myocardial Infarction - surgery
/ Myocardium - cytology
/ Myocardium - metabolism
/ Myocardium - pathology
/ Neovascularization, Physiologic
/ Proteins
/ Rats
/ Rats, Sprague-Dawley
/ Rodents
/ Stem cells
/ Vascular endothelial growth factor
/ Ventricular Remodeling
2010
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Over-expression of HO-1 on mesenchymal stem cells promotes angiogenesis and improves myocardial function in infarcted myocardium
by
Zhang, Yan
, Lin, Guosheng
, Zeng, Bin
, Ren, Xiaofeng
, Chen, Honglei
in
Animals
/ Apoptosis
/ Biomedical and Life Sciences
/ Biomedicine
/ Bone marrow
/ Enzymes
/ Fibroblast growth factors
/ Gene therapy
/ Growth factors
/ Heart attacks
/ Heme
/ Heme Oxygenase-1 - genetics
/ Heme Oxygenase-1 - metabolism
/ Hemodynamics
/ In Situ Nick-End Labeling
/ Male
/ Mesenchymal Stem Cell Transplantation
/ Mesenchymal Stromal Cells - metabolism
/ Myocardial infarction
/ Myocardial Infarction - metabolism
/ Myocardial Infarction - pathology
/ Myocardial Infarction - surgery
/ Myocardium - cytology
/ Myocardium - metabolism
/ Myocardium - pathology
/ Neovascularization, Physiologic
/ Proteins
/ Rats
/ Rats, Sprague-Dawley
/ Rodents
/ Stem cells
/ Vascular endothelial growth factor
/ Ventricular Remodeling
2010
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Over-expression of HO-1 on mesenchymal stem cells promotes angiogenesis and improves myocardial function in infarcted myocardium
Journal Article
Over-expression of HO-1 on mesenchymal stem cells promotes angiogenesis and improves myocardial function in infarcted myocardium
2010
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Overview
Heme oxygenase-1 (HO-1) is a stress-inducible enzyme with diverse cytoprotective effects, and reported to have an important role in angiogenesis recently. Here we investigated whether HO-1 transduced by mesenchymal stem cells (MSCs) can induce angiogenic effects in infarcted myocardium. HO-1 was transfected into cultured MSCs using an adenoviral vector. 1 × 10
6
Ad-HO-1-transfected MSCs (HO-1-MSCs) or Ad-Null-transfected MSCs (Null-MSCs) or PBS was respectively injected into rat hearts intramyocardially at 1 h post-myocardial infarction. The results showed that HO-1-MSCs were able to induce stable expression of HO-1
in vitro
and
in vivo
. The capillary density and expression of angiogenic growth factors, VEGF and FGF2 were significantly enhanced in HO-1-MSCs-treated hearts compared with Null-MSCs-treated and PBS-treated hearts. However, the angiogenic effects of HO-1 were abolished by treating the animals with HO inhibitor, zinc protoporphyrin. The myocardial apoptosis was marked reduced with significantly reduced fibrotic area in HO-1-MSCs-treated hearts; Furthermore, the cardiac function and remodeling were also significantly improved in HO-1-MSCs-treated hearts. Our current findings support the premise that HO-1 transduced by MSCs can induce angiogenic effects and improve heart function after acute myocardial infarction.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Biomedical and Life Sciences
/ Enzymes
/ Heme
/ Heme Oxygenase-1 - metabolism
/ Male
/ Mesenchymal Stem Cell Transplantation
/ Mesenchymal Stromal Cells - metabolism
/ Myocardial Infarction - metabolism
/ Myocardial Infarction - pathology
/ Myocardial Infarction - surgery
/ Neovascularization, Physiologic
/ Proteins
/ Rats
/ Rodents
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