The decrement in circulating endothelial progenitor cells (EPCs) in type 2 diabetes is independent of the severity of the hypoadiponectemia

Background Type 2 diabetes mellitus (DM) is associated with a decreased level of circulating endothelial progenitor cells (EPCs) and adiponectin. Experimental studies suggest a potential link between hypoadiponectinaemia and the depletion of the EPC level. This study investigated the relationships b...

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Veröffentlicht in:Diabetes/metabolism research and reviews 2011-02, Vol.27 (2), p.185-194
Hauptverfasser: Li, Mingfang, Ho, Jenny C. Y., Lai, Kevin W. H., Au, Karen K. W., Xu, Aimin, Cheung, Bernard M. Y., Lam, Karen S. L., Tse, Hung-Fat
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container_end_page 194
container_issue 2
container_start_page 185
container_title Diabetes/metabolism research and reviews
container_volume 27
creator Li, Mingfang
Ho, Jenny C. Y.
Lai, Kevin W. H.
Au, Karen K. W.
Xu, Aimin
Cheung, Bernard M. Y.
Lam, Karen S. L.
Tse, Hung-Fat
description Background Type 2 diabetes mellitus (DM) is associated with a decreased level of circulating endothelial progenitor cells (EPCs) and adiponectin. Experimental studies suggest a potential link between hypoadiponectinaemia and the depletion of the EPC level. This study investigated the relationships between adiponectin level and EPC in patients with type 2 DM. Methods A total of 95 type 2 DM patients (58.5 ± 8.8 years, 42 men) and 95 age‐ and sex‐matched healthy controls were recruited. Circulating EPC levels were determined by flow cytometry using CD133+, CD34+, CD133+/KDR+ and CD34+/KDR+ as surface markers. Plasma adiponectin levels were measured by enzyme‐linked immunosorbent assay. EPC function was studied by in vitro tube formation and migration assay. Results The levels of CD133+ (p < 0.001) and CD133+/KDR+ (p < 0.001) EPCs were independently associated with the presence of type 2 DM. The levels of CD34+ (p = 0.004) and CD34+/KDR+ (p = 0.013) EPCs were independently associated with haemoglobin A$_{\rm{1c}}$. Nevertheless, there was no relationship between the number of EPCs and adiponectin level. Tube formation assay showed impaired pro‐angiogenic function of EPC in DM patients compared with controls (p = 0.007). Interestingly, adiponectin supplementation (5 µg/mL) increased tube formation by 17.6% in EPCs from DM patients (p = 0.002). It also significantly enhanced cell migration by 35.9% in EPCs from DM patients (p = 0.01). Conclusions We detected no relationship between the reduction in the level of EPC and in the level of total adiponectin in blood from patients with type 2 diabetes. EPC from patients with diabetes were stimulated when exposed to adiponectin in the test tube, findings that warrant further study. Copyright © 2011 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/dmrr.1159
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Y. ; Lai, Kevin W. H. ; Au, Karen K. W. ; Xu, Aimin ; Cheung, Bernard M. Y. ; Lam, Karen S. L. ; Tse, Hung-Fat</creator><creatorcontrib>Li, Mingfang ; Ho, Jenny C. Y. ; Lai, Kevin W. H. ; Au, Karen K. W. ; Xu, Aimin ; Cheung, Bernard M. Y. ; Lam, Karen S. L. ; Tse, Hung-Fat</creatorcontrib><description>Background Type 2 diabetes mellitus (DM) is associated with a decreased level of circulating endothelial progenitor cells (EPCs) and adiponectin. Experimental studies suggest a potential link between hypoadiponectinaemia and the depletion of the EPC level. This study investigated the relationships between adiponectin level and EPC in patients with type 2 DM. Methods A total of 95 type 2 DM patients (58.5 ± 8.8 years, 42 men) and 95 age‐ and sex‐matched healthy controls were recruited. Circulating EPC levels were determined by flow cytometry using CD133+, CD34+, CD133+/KDR+ and CD34+/KDR+ as surface markers. Plasma adiponectin levels were measured by enzyme‐linked immunosorbent assay. EPC function was studied by in vitro tube formation and migration assay. Results The levels of CD133+ (p &lt; 0.001) and CD133+/KDR+ (p &lt; 0.001) EPCs were independently associated with the presence of type 2 DM. The levels of CD34+ (p = 0.004) and CD34+/KDR+ (p = 0.013) EPCs were independently associated with haemoglobin A$_{\rm{1c}}$. Nevertheless, there was no relationship between the number of EPCs and adiponectin level. Tube formation assay showed impaired pro‐angiogenic function of EPC in DM patients compared with controls (p = 0.007). Interestingly, adiponectin supplementation (5 µg/mL) increased tube formation by 17.6% in EPCs from DM patients (p = 0.002). It also significantly enhanced cell migration by 35.9% in EPCs from DM patients (p = 0.01). Conclusions We detected no relationship between the reduction in the level of EPC and in the level of total adiponectin in blood from patients with type 2 diabetes. EPC from patients with diabetes were stimulated when exposed to adiponectin in the test tube, findings that warrant further study. Copyright © 2011 John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 1520-7552</identifier><identifier>EISSN: 1520-7560</identifier><identifier>DOI: 10.1002/dmrr.1159</identifier><identifier>PMID: 21294240</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>adiponectin ; Adiponectin - blood ; Case-Control Studies ; Cells, Cultured ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - pathology ; endothelial progenitor cells ; Endothelium, Vascular - cytology ; Endothelium, Vascular - metabolism ; Female ; Humans ; Male ; Middle Aged ; Stem Cells - metabolism ; type 2 diabetes mellitus ; Umbilical Veins - cytology ; Umbilical Veins - metabolism</subject><ispartof>Diabetes/metabolism research and reviews, 2011-02, Vol.27 (2), p.185-194</ispartof><rights>Copyright © 2011 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4289-c6853716cbbb87ba2bab577dd252d6119737ff0b7c7f7a083209e909ee433cf83</citedby><cites>FETCH-LOGICAL-c4289-c6853716cbbb87ba2bab577dd252d6119737ff0b7c7f7a083209e909ee433cf83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdmrr.1159$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdmrr.1159$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21294240$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Mingfang</creatorcontrib><creatorcontrib>Ho, Jenny C. Y.</creatorcontrib><creatorcontrib>Lai, Kevin W. H.</creatorcontrib><creatorcontrib>Au, Karen K. W.</creatorcontrib><creatorcontrib>Xu, Aimin</creatorcontrib><creatorcontrib>Cheung, Bernard M. Y.</creatorcontrib><creatorcontrib>Lam, Karen S. L.</creatorcontrib><creatorcontrib>Tse, Hung-Fat</creatorcontrib><title>The decrement in circulating endothelial progenitor cells (EPCs) in type 2 diabetes is independent of the severity of the hypoadiponectemia</title><title>Diabetes/metabolism research and reviews</title><addtitle>Diabetes Metab. Res. Rev</addtitle><description>Background Type 2 diabetes mellitus (DM) is associated with a decreased level of circulating endothelial progenitor cells (EPCs) and adiponectin. Experimental studies suggest a potential link between hypoadiponectinaemia and the depletion of the EPC level. This study investigated the relationships between adiponectin level and EPC in patients with type 2 DM. Methods A total of 95 type 2 DM patients (58.5 ± 8.8 years, 42 men) and 95 age‐ and sex‐matched healthy controls were recruited. Circulating EPC levels were determined by flow cytometry using CD133+, CD34+, CD133+/KDR+ and CD34+/KDR+ as surface markers. Plasma adiponectin levels were measured by enzyme‐linked immunosorbent assay. EPC function was studied by in vitro tube formation and migration assay. Results The levels of CD133+ (p &lt; 0.001) and CD133+/KDR+ (p &lt; 0.001) EPCs were independently associated with the presence of type 2 DM. The levels of CD34+ (p = 0.004) and CD34+/KDR+ (p = 0.013) EPCs were independently associated with haemoglobin A$_{\rm{1c}}$. Nevertheless, there was no relationship between the number of EPCs and adiponectin level. Tube formation assay showed impaired pro‐angiogenic function of EPC in DM patients compared with controls (p = 0.007). Interestingly, adiponectin supplementation (5 µg/mL) increased tube formation by 17.6% in EPCs from DM patients (p = 0.002). It also significantly enhanced cell migration by 35.9% in EPCs from DM patients (p = 0.01). Conclusions We detected no relationship between the reduction in the level of EPC and in the level of total adiponectin in blood from patients with type 2 diabetes. EPC from patients with diabetes were stimulated when exposed to adiponectin in the test tube, findings that warrant further study. Copyright © 2011 John Wiley &amp; Sons, Ltd.</description><subject>adiponectin</subject><subject>Adiponectin - blood</subject><subject>Case-Control Studies</subject><subject>Cells, Cultured</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - pathology</subject><subject>endothelial progenitor cells</subject><subject>Endothelium, Vascular - cytology</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Stem Cells - metabolism</subject><subject>type 2 diabetes mellitus</subject><subject>Umbilical Veins - cytology</subject><subject>Umbilical Veins - metabolism</subject><issn>1520-7552</issn><issn>1520-7560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtu1DAUhi1ERUthwQsg76CLtL4kcbJE06vUC1QFJDaWLycdQ27YHto8Q1-6jmY6OyRbPpa-_5POj9AHSg4pIezIdt4fUlrUr9AeLRjJRFGS19u5YLvobQi_CSE8L_M3aJdRVucsJ3vo6W4J2ILx0EEfseuxcd6sWhVdf4-ht0NcQutUi0c_3EPv4uCxgbYN-PPJ10U4mCNxGgEzbJ3SECFgl05vYUzxWTo0OElwgH_gXZxe_stpHJR149CDidA59Q7tNKoN8H7z7qPvpyd3i_Ps8ubsYvHlMjM5q-rMlFXBBS2N1roSWjGtdCGEtaxgtqS0Flw0DdHCiEYoUnFGaqjThZxz01R8H31ae9NKf1cQouxcmHdSPQyrIKs8lVOLnCXyYE0aP4TgoZGjd53yk6REztXLuXo5V5_YjxvrSndgt-RL1wk4WgMProXp_yZ5fHV7u1Fm64QLER63CeX_yDItWcif12ey_Hb6q1r84FLwZzMKnyw</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Li, Mingfang</creator><creator>Ho, Jenny C. 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L. ; Tse, Hung-Fat</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4289-c6853716cbbb87ba2bab577dd252d6119737ff0b7c7f7a083209e909ee433cf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>adiponectin</topic><topic>Adiponectin - blood</topic><topic>Case-Control Studies</topic><topic>Cells, Cultured</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - pathology</topic><topic>endothelial progenitor cells</topic><topic>Endothelium, Vascular - cytology</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Stem Cells - metabolism</topic><topic>type 2 diabetes mellitus</topic><topic>Umbilical Veins - cytology</topic><topic>Umbilical Veins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Mingfang</creatorcontrib><creatorcontrib>Ho, Jenny C. Y.</creatorcontrib><creatorcontrib>Lai, Kevin W. H.</creatorcontrib><creatorcontrib>Au, Karen K. W.</creatorcontrib><creatorcontrib>Xu, Aimin</creatorcontrib><creatorcontrib>Cheung, Bernard M. Y.</creatorcontrib><creatorcontrib>Lam, Karen S. L.</creatorcontrib><creatorcontrib>Tse, Hung-Fat</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes/metabolism research and reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Mingfang</au><au>Ho, Jenny C. Y.</au><au>Lai, Kevin W. H.</au><au>Au, Karen K. W.</au><au>Xu, Aimin</au><au>Cheung, Bernard M. Y.</au><au>Lam, Karen S. L.</au><au>Tse, Hung-Fat</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The decrement in circulating endothelial progenitor cells (EPCs) in type 2 diabetes is independent of the severity of the hypoadiponectemia</atitle><jtitle>Diabetes/metabolism research and reviews</jtitle><addtitle>Diabetes Metab. Res. Rev</addtitle><date>2011-02</date><risdate>2011</risdate><volume>27</volume><issue>2</issue><spage>185</spage><epage>194</epage><pages>185-194</pages><issn>1520-7552</issn><eissn>1520-7560</eissn><abstract>Background Type 2 diabetes mellitus (DM) is associated with a decreased level of circulating endothelial progenitor cells (EPCs) and adiponectin. Experimental studies suggest a potential link between hypoadiponectinaemia and the depletion of the EPC level. This study investigated the relationships between adiponectin level and EPC in patients with type 2 DM. Methods A total of 95 type 2 DM patients (58.5 ± 8.8 years, 42 men) and 95 age‐ and sex‐matched healthy controls were recruited. Circulating EPC levels were determined by flow cytometry using CD133+, CD34+, CD133+/KDR+ and CD34+/KDR+ as surface markers. Plasma adiponectin levels were measured by enzyme‐linked immunosorbent assay. EPC function was studied by in vitro tube formation and migration assay. Results The levels of CD133+ (p &lt; 0.001) and CD133+/KDR+ (p &lt; 0.001) EPCs were independently associated with the presence of type 2 DM. The levels of CD34+ (p = 0.004) and CD34+/KDR+ (p = 0.013) EPCs were independently associated with haemoglobin A$_{\rm{1c}}$. Nevertheless, there was no relationship between the number of EPCs and adiponectin level. Tube formation assay showed impaired pro‐angiogenic function of EPC in DM patients compared with controls (p = 0.007). Interestingly, adiponectin supplementation (5 µg/mL) increased tube formation by 17.6% in EPCs from DM patients (p = 0.002). It also significantly enhanced cell migration by 35.9% in EPCs from DM patients (p = 0.01). Conclusions We detected no relationship between the reduction in the level of EPC and in the level of total adiponectin in blood from patients with type 2 diabetes. EPC from patients with diabetes were stimulated when exposed to adiponectin in the test tube, findings that warrant further study. Copyright © 2011 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>21294240</pmid><doi>10.1002/dmrr.1159</doi><tpages>10</tpages></addata></record>
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subjects adiponectin
Adiponectin - blood
Case-Control Studies
Cells, Cultured
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - pathology
endothelial progenitor cells
Endothelium, Vascular - cytology
Endothelium, Vascular - metabolism
Female
Humans
Male
Middle Aged
Stem Cells - metabolism
type 2 diabetes mellitus
Umbilical Veins - cytology
Umbilical Veins - metabolism
title The decrement in circulating endothelial progenitor cells (EPCs) in type 2 diabetes is independent of the severity of the hypoadiponectemia
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