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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 |
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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. |
doi_str_mv | 10.5966/sctm.2013-0014 |
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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.</description><identifier>ISSN: 2157-6564</identifier><identifier>EISSN: 2157-6580</identifier><identifier>DOI: 10.5966/sctm.2013-0014</identifier><identifier>PMID: 24353175</identifier><language>eng</language><publisher>Durham, NC, USA: AlphaMed Press</publisher><subject>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</subject><ispartof>Stem cells translational medicine, 2014-01, Vol.3 (1), p.32-41</ispartof><rights>2014 AlphaMed Press</rights><rights>2014. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). 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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.</description><subject>Adipose Tissue - cytology</subject><subject>Adipose-derived stromal cells</subject><subject>Administrative support</subject><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Aging</subject><subject>Aging - physiology</subject><subject>Angina pectoris</subject><subject>Angiogenesis</subject><subject>Angiopoietin-1 - metabolism</subject><subject>Atherosclerosis</subject><subject>Bone marrow</subject><subject>Cardiology</subject><subject>Cardiovascular disease</subject><subject>Cell therapy</subject><subject>Cellular Senescence - physiology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Coronary artery</subject><subject>Coronary artery disease</subject><subject>Coronary Artery Disease - pathology</subject><subject>Coronary vessels</subject><subject>Culture Media, Conditioned - pharmacology</subject><subject>Data analysis</subject><subject>Diabetes</subject><subject>Female</subject><subject>Heart diseases</subject><subject>Heart failure</subject><subject>Hepatocyte Growth Factor - metabolism</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension - pathology</subject><subject>Ischemia</subject><subject>Male</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>Mesenchymal Stromal Cells - drug effects</subject><subject>Mesenchymal Stromal Cells - metabolism</subject><subject>Mesenchyme</subject><subject>Middle Aged</subject><subject>Neovascularization, Physiologic - physiology</subject><subject>Pathology</subject><subject>Patients</subject><subject>Secretion</subject><subject>Stromal cells</subject><subject>Studies</subject><subject>Surgery</subject><subject>Therapeutic angiogenesis</subject><subject>Tissue-Specific Progenitor and Stem Cells</subject><subject>Urokinase receptor</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>2157-6564</issn><issn>2157-6580</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqFks1u1DAURiMEolXpliWyxIbNDP5JnHiDNEpbWlHESC1iaTnOTeIqiYPtmTI7HoFH4xl4EhxNGQESwptry8fH19aXJM8JXmaC89deh2FJMWELjEn6KDmmJMsXPCvw48Ocp0fJqfd3OA4uuKD4aXJEU5YxkmfHyfdVbSbr4cfXb2fgzBZq9B48jLrbDapHN8HZuZbQ9x5dxAVatZFZq2BgDB59MqFDpXV2VG6HVi5ALGfGg_KA3gFM_9ShtbMTuOjxqNoEdP6lM5UJqOyUUzp6jA9Ge2SbeKUZW6TGGl2qLaCrYVLGxS5WY2tsC6PRaG1D7Meo_lnypFG9h9OHepJ8vDi_LS8X1x_eXpWr64VOeU4XJCOCqaoGARVOBQAualAVVwAiowwDyzHheVFrWqd1VnGmmzzHtGmyOgPK2UnyZu-dNtUAtY63O9XLyZkh_oS0ysg_d0bTydZuJROY0oJFwasHgbOfN-CDHIzX8WPUCHbjJUkFznNOxYy-_Au9sxs3xudJSoUgtEiLIlLLPaWd9d5Bc2iGYDnnRc55kXNe5JyXeODF70844L_SEYFiD9ybHnb_0cmb8pbR2UsYZT8Bo5fTAQ</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Efimenko, Anastasia</creator><creator>Dzhoyashvili, Nina</creator><creator>Kalinina, Natalia</creator><creator>Kochegura, Tatiana</creator><creator>Akchurin, Renat</creator><creator>Tkachuk, Vsevolod</creator><creator>Parfyonova, Yelena</creator><general>AlphaMed Press</general><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201401</creationdate><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</title><author>Efimenko, Anastasia ; Dzhoyashvili, Nina ; Kalinina, Natalia ; Kochegura, Tatiana ; Akchurin, Renat ; Tkachuk, Vsevolod ; Parfyonova, Yelena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4672-15193abde9eb049ee08deab6aee95230e3701678dc2d4d5b63cf7702ff5d5e263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adipose Tissue - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Stem cells translational medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Efimenko, Anastasia</au><au>Dzhoyashvili, Nina</au><au>Kalinina, Natalia</au><au>Kochegura, Tatiana</au><au>Akchurin, Renat</au><au>Tkachuk, Vsevolod</au><au>Parfyonova, Yelena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Stem cells translational medicine</jtitle><addtitle>Stem Cells Transl Med</addtitle><date>2014-01</date><risdate>2014</risdate><volume>3</volume><issue>1</issue><spage>32</spage><epage>41</epage><pages>32-41</pages><issn>2157-6564</issn><eissn>2157-6580</eissn><abstract>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.</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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