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Adipose‐Derived Mesenchymal Stromal Cells From Aged Patients With Coronary Artery Disease Keep Mesenchymal Stromal Cell Properties but Exhibit Characteristics of Aging and Have Impaired Angiogenic Potential

This study analyzed how patient age affected the angiogenic properties of adipose‐derived mesenchymal stromal cells (ADSCs). ADSCs from aged patients both with and without coronary artery disease acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogen...

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Published in:Stem cells translational medicine 2014-01, Vol.3 (1), p.32-41
Main Authors: Efimenko, Anastasia, Dzhoyashvili, Nina, Kalinina, Natalia, Kochegura, Tatiana, Akchurin, Renat, Tkachuk, Vsevolod, Parfyonova, Yelena
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creator Efimenko, Anastasia
Dzhoyashvili, Nina
Kalinina, Natalia
Kochegura, Tatiana
Akchurin, Renat
Tkachuk, Vsevolod
Parfyonova, Yelena
description This study analyzed how patient age affected the angiogenic properties of adipose‐derived mesenchymal stromal cells (ADSCs). ADSCs from aged patients both with and without coronary artery disease acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogenic factor secretion. This could restrict the effectiveness of autologous cell therapy with ADSCs in aged patients. Tissue regeneration is impaired in aged individuals. Adipose‐derived mesenchymal stromal cells (ADSCs), a promising source for cell therapy, were shown to secrete various angiogenic factors and improve vascularization of ischemic tissues. We analyzed how patient age affected the angiogenic properties of ADSCs. ADSCs were isolated from subcutaneous fat tissue of patients with coronary artery disease (CAD; n = 64, 43–77 years old) and without CAD (n = 31, 2–82 years old). ADSC phenotype characterized by flow cytometry was CD90+/CD73+/CD105+/CD45−/CD31− for all samples, and these cells were capable of adipogenic and osteogenic differentiation. ADSCs from aged patients had shorter telomeres (quantitative reverse transcription polymerase chain reaction) and a tendency to attenuated telomerase activity. ADSC‐conditioned media (ADSC‐CM) stimulated capillary‐like tube formation by endothelial cells (EA.hy926), and this effect significantly decreased with the age of patients both with and without CAD. Angiogenic factors (vascular endothelial growth factor, placental growth factor, hepatocyte growth factor, angiopoetin‐1, and angiogenin) in ADSC‐CM measured by enzyme‐linked immunosorbent assay significantly decreased with patient age, whereas levels of antiangiogenic factors thrombospondin‐1 and endostatin did not. Expression of angiogenic factors in ADSCs did not change with patient age (real‐time polymerase chain reaction); however, gene expression of factors related to extracellular proteolysis (urokinase and its receptor, plasminogen activator inhibitor‐1) and urokinase‐type plasminogen activator receptor surface expression increased in ADSCs from aged patients with CAD. ADSCs from aged patients both with and without CAD acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogenic factor secretion. This could restrict the effectiveness of autologous cell therapy with ADSCs in aged patients.
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ADSCs from aged patients both with and without coronary artery disease acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogenic factor secretion. This could restrict the effectiveness of autologous cell therapy with ADSCs in aged patients. Tissue regeneration is impaired in aged individuals. Adipose‐derived mesenchymal stromal cells (ADSCs), a promising source for cell therapy, were shown to secrete various angiogenic factors and improve vascularization of ischemic tissues. We analyzed how patient age affected the angiogenic properties of ADSCs. ADSCs were isolated from subcutaneous fat tissue of patients with coronary artery disease (CAD; n = 64, 43–77 years old) and without CAD (n = 31, 2–82 years old). ADSC phenotype characterized by flow cytometry was CD90+/CD73+/CD105+/CD45−/CD31− for all samples, and these cells were capable of adipogenic and osteogenic differentiation. ADSCs from aged patients had shorter telomeres (quantitative reverse transcription polymerase chain reaction) and a tendency to attenuated telomerase activity. ADSC‐conditioned media (ADSC‐CM) stimulated capillary‐like tube formation by endothelial cells (EA.hy926), and this effect significantly decreased with the age of patients both with and without CAD. Angiogenic factors (vascular endothelial growth factor, placental growth factor, hepatocyte growth factor, angiopoetin‐1, and angiogenin) in ADSC‐CM measured by enzyme‐linked immunosorbent assay significantly decreased with patient age, whereas levels of antiangiogenic factors thrombospondin‐1 and endostatin did not. Expression of angiogenic factors in ADSCs did not change with patient age (real‐time polymerase chain reaction); however, gene expression of factors related to extracellular proteolysis (urokinase and its receptor, plasminogen activator inhibitor‐1) and urokinase‐type plasminogen activator receptor surface expression increased in ADSCs from aged patients with CAD. ADSCs from aged patients both with and without CAD acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogenic factor secretion. 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Expression of angiogenic factors in ADSCs did not change with patient age (real‐time polymerase chain reaction); however, gene expression of factors related to extracellular proteolysis (urokinase and its receptor, plasminogen activator inhibitor‐1) and urokinase‐type plasminogen activator receptor surface expression increased in ADSCs from aged patients with CAD. ADSCs from aged patients both with and without CAD acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogenic factor secretion. 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ADSCs from aged patients both with and without coronary artery disease acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogenic factor secretion. This could restrict the effectiveness of autologous cell therapy with ADSCs in aged patients. Tissue regeneration is impaired in aged individuals. Adipose‐derived mesenchymal stromal cells (ADSCs), a promising source for cell therapy, were shown to secrete various angiogenic factors and improve vascularization of ischemic tissues. We analyzed how patient age affected the angiogenic properties of ADSCs. ADSCs were isolated from subcutaneous fat tissue of patients with coronary artery disease (CAD; n = 64, 43–77 years old) and without CAD (n = 31, 2–82 years old). ADSC phenotype characterized by flow cytometry was CD90+/CD73+/CD105+/CD45−/CD31− for all samples, and these cells were capable of adipogenic and osteogenic differentiation. ADSCs from aged patients had shorter telomeres (quantitative reverse transcription polymerase chain reaction) and a tendency to attenuated telomerase activity. ADSC‐conditioned media (ADSC‐CM) stimulated capillary‐like tube formation by endothelial cells (EA.hy926), and this effect significantly decreased with the age of patients both with and without CAD. Angiogenic factors (vascular endothelial growth factor, placental growth factor, hepatocyte growth factor, angiopoetin‐1, and angiogenin) in ADSC‐CM measured by enzyme‐linked immunosorbent assay significantly decreased with patient age, whereas levels of antiangiogenic factors thrombospondin‐1 and endostatin did not. Expression of angiogenic factors in ADSCs did not change with patient age (real‐time polymerase chain reaction); however, gene expression of factors related to extracellular proteolysis (urokinase and its receptor, plasminogen activator inhibitor‐1) and urokinase‐type plasminogen activator receptor surface expression increased in ADSCs from aged patients with CAD. ADSCs from aged patients both with and without CAD acquire aging characteristics, and their angiogenic potential declines because of decreasing proangiogenic factor secretion. This could restrict the effectiveness of autologous cell therapy with ADSCs in aged patients.</abstract><cop>Durham, NC, USA</cop><pub>AlphaMed Press</pub><pmid>24353175</pmid><doi>10.5966/sctm.2013-0014</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Adipose Tissue - cytology
Adipose-derived stromal cells
Administrative support
Adult
Age
Aged
Aging
Aging - physiology
Angina pectoris
Angiogenesis
Angiopoietin-1 - metabolism
Atherosclerosis
Bone marrow
Cardiology
Cardiovascular disease
Cell therapy
Cellular Senescence - physiology
Child
Child, Preschool
Coronary artery
Coronary artery disease
Coronary Artery Disease - pathology
Coronary vessels
Culture Media, Conditioned - pharmacology
Data analysis
Diabetes
Female
Heart diseases
Heart failure
Hepatocyte Growth Factor - metabolism
Humans
Hypertension
Hypertension - pathology
Ischemia
Male
Mesenchymal stem cells
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - drug effects
Mesenchymal Stromal Cells - metabolism
Mesenchyme
Middle Aged
Neovascularization, Physiologic - physiology
Pathology
Patients
Secretion
Stromal cells
Studies
Surgery
Therapeutic angiogenesis
Tissue-Specific Progenitor and Stem Cells
Urokinase receptor
Vascular Endothelial Growth Factor A - metabolism
title Adipose‐Derived Mesenchymal Stromal Cells From Aged Patients With Coronary Artery Disease Keep Mesenchymal Stromal Cell Properties but Exhibit Characteristics of Aging and Have Impaired Angiogenic Potential
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