<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nowak WN</submitter><funding>Jagiellonian University Medical College</funding><funding>European Union Innovative Economy Programme</funding><pagination>99-107</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4025239</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>&lt;h4>Aims/introduction&lt;/h4>Type 2 diabetes is often complicated by diabetic foot syndrome (DFS). We analyzed the circulating stem cells, growth factor and anti-oxidant gene expression profiles in type 2 diabetes patients without or with different forms of DFS.&lt;h4>Materials and methods&lt;/h4>Healthy volunteers (n = 13) and type 2 diabetes patients: (i) without DFS (n = 10); or with (ii) Charcot osteoneuropathy (n = 10); (iii) non-infected (n = 17); (iv) infected (n = 11); and (v) healed ulceration were examined (n = 12). Peripheral blood endothelial progenitor cells (EPC), mesenchymal stem cells (MSC), hematopoietic stem cells (HSC) and very small embryonic-like (VSEL) cells were phenotyped using flow cytometry. Plasma cytokine concentrations and gene expressions in blood cells were measured by Luminex and quantitative real-time polymerase chain reaction assays, respectively.&lt;h4>Results&lt;/h4>Patients with non-complicated type 2 diabetes showed reduced HMOX1 expression, accompanied by HMOX2 upregulation, and had less circulating EPC, MSC or HSC than healthy subjects. In contrast, VSEL cells were elevated in the type 2 diabetes group. However, subjects with DFS, even with healed ulceration, had fewer VSEL cells, more CD45-CD29(+)CD90(+)MSC, and upregulated HMOX1 when compared with the type 2 diabetes group. Patients with Charcot osteopathy had lowered plasma fibroblast growth factor-2. Elevated plasma tumor necrosis factor-α and decreased catalase expression was found in all diabetic patients.&lt;h4>Conclusions&lt;/h4>Patients with type 2 diabetes and different forms of DFS have an altered number of circulating stem cells. Type 2 diabetes might also be associated with a changed plasma growth factor and anti-oxidant gene expression profile. Altogether, these factors could contribute to the pathogenesis of different forms of DFS.</pubmed_abstract><journal>Journal of diabetes investigation</journal><pubmed_title>Number of circulating pro-angiogenic cells, growth factor and anti-oxidative gene profiles might be altered in type 2 diabetes with and without diabetic foot syndrome.</pubmed_title><pmcid>PMC4025239</pmcid><funding_grant_id>02.02.00-00-014/08</funding_grant_id><funding_grant_id>01.01.02.069/09</funding_grant_id><funding_grant_id>02.01.00-12-064/08</funding_grant_id><funding_grant_id>K/ZDS/002808</funding_grant_id><funding_grant_id>POIG 01.01.02-00-109/09</funding_grant_id><pubmed_authors>Dulak J</pubmed_authors><pubmed_authors>Bukowska-Strakova K</pubmed_authors><pubmed_authors>Witek P</pubmed_authors><pubmed_authors>Borys S</pubmed_authors><pubmed_authors>Kusinska K</pubmed_authors><pubmed_authors>Jozkowicz A</pubmed_authors><pubmed_authors>Koblik T</pubmed_authors><pubmed_authors>Malecki MT</pubmed_authors><pubmed_authors>Nowak WN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Number of circulating pro-angiogenic cells, growth factor and anti-oxidative gene profiles might be altered in type 2 diabetes with and without diabetic foot syndrome.</name><description>&lt;h4>Aims/introduction&lt;/h4>Type 2 diabetes is often complicated by diabetic foot syndrome (DFS). We analyzed the circulating stem cells, growth factor and anti-oxidant gene expression profiles in type 2 diabetes patients without or with different forms of DFS.&lt;h4>Materials and methods&lt;/h4>Healthy volunteers (n = 13) and type 2 diabetes patients: (i) without DFS (n = 10); or with (ii) Charcot osteoneuropathy (n = 10); (iii) non-infected (n = 17); (iv) infected (n = 11); and (v) healed ulceration were examined (n = 12). Peripheral blood endothelial progenitor cells (EPC), mesenchymal stem cells (MSC), hematopoietic stem cells (HSC) and very small embryonic-like (VSEL) cells were phenotyped using flow cytometry. Plasma cytokine concentrations and gene expressions in blood cells were measured by Luminex and quantitative real-time polymerase chain reaction assays, respectively.&lt;h4>Results&lt;/h4>Patients with non-complicated type 2 diabetes showed reduced HMOX1 expression, accompanied by HMOX2 upregulation, and had less circulating EPC, MSC or HSC than healthy subjects. In contrast, VSEL cells were elevated in the type 2 diabetes group. However, subjects with DFS, even with healed ulceration, had fewer VSEL cells, more CD45-CD29(+)CD90(+)MSC, and upregulated HMOX1 when compared with the type 2 diabetes group. Patients with Charcot osteopathy had lowered plasma fibroblast growth factor-2. Elevated plasma tumor necrosis factor-α and decreased catalase expression was found in all diabetic patients.&lt;h4>Conclusions&lt;/h4>Patients with type 2 diabetes and different forms of DFS have an altered number of circulating stem cells. Type 2 diabetes might also be associated with a changed plasma growth factor and anti-oxidant gene expression profile. Altogether, these factors could contribute to the pathogenesis of different forms of DFS.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Feb</publication><modification>2025-04-05T13:37:31.547Z</modification><creation>2019-03-27T01:28:27Z</creation></dates><accession>S-EPMC4025239</accession><cross_references><pubmed>24843745</pubmed><doi>10.1111/jdi.12131</doi></cross_references></HashMap>