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Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control

BACKGROUND: Endothelial progenitor cells (EPCs) play an important role in vascular repair and a decrease in the number of EPCs is observed in type 2 diabetes. However, there is no report on the change of EPCs after glycemic control. This study therefore aimed to investigate the EPC number and functi...

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Autores principales: Churdchomjan, Worachat, Kheolamai, Pakpoom, Manochantr, Sirikul, Tapanadechopone, Pirath, Tantrawatpan, Chairat, U-pratya, Yaowalak, Issaragrisil, Surapol
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858721/
https://www.ncbi.nlm.nih.gov/pubmed/20374643
http://dx.doi.org/10.1186/1472-6823-10-5
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author Churdchomjan, Worachat
Kheolamai, Pakpoom
Manochantr, Sirikul
Tapanadechopone, Pirath
Tantrawatpan, Chairat
U-pratya, Yaowalak
Issaragrisil, Surapol
author_facet Churdchomjan, Worachat
Kheolamai, Pakpoom
Manochantr, Sirikul
Tapanadechopone, Pirath
Tantrawatpan, Chairat
U-pratya, Yaowalak
Issaragrisil, Surapol
author_sort Churdchomjan, Worachat
collection PubMed
description BACKGROUND: Endothelial progenitor cells (EPCs) play an important role in vascular repair and a decrease in the number of EPCs is observed in type 2 diabetes. However, there is no report on the change of EPCs after glycemic control. This study therefore aimed to investigate the EPC number and function in patients with good and poor glycemic control. METHODS: The number of EPCs was studied using flow cytometry by co-expression of CD34 and VEGFR2. The EPCs were cultured and characterized by the expression of UEA-I, CD34, VEGFR2, vWF and Dil-Ac-LDL engulfment, as well as the ability to form capillary-like structures. An in vitro study on the effect of hyperglycemia on the proliferation and viability of the cultured EPCs was also performed. RESULTS: The number of EPCs in type 2 diabetes was significantly decreased compared with healthy controls and there was an inverse correlation between the EPC numbers and plasma glucose, as well as HbA1(C). The number and function of EPCs in patients with good glycemic control were recovered compared with those with poor glycemic control. When glucose was supplemented in the culture in vitro, there was a negative effect on the proliferation and viability of EPCs, in a dose-dependent manner, whereas the enhancement of apoptosis was observed. CONCLUSION: There was EPC dysfunction in type 2 diabetes which might be improved by strict glycemic control. However, the circulating EPC number and proliferative function in patients with good glycemic control did not reach the level in healthy controls.
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spelling pubmed-28587212010-04-23 Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control Churdchomjan, Worachat Kheolamai, Pakpoom Manochantr, Sirikul Tapanadechopone, Pirath Tantrawatpan, Chairat U-pratya, Yaowalak Issaragrisil, Surapol BMC Endocr Disord Research article BACKGROUND: Endothelial progenitor cells (EPCs) play an important role in vascular repair and a decrease in the number of EPCs is observed in type 2 diabetes. However, there is no report on the change of EPCs after glycemic control. This study therefore aimed to investigate the EPC number and function in patients with good and poor glycemic control. METHODS: The number of EPCs was studied using flow cytometry by co-expression of CD34 and VEGFR2. The EPCs were cultured and characterized by the expression of UEA-I, CD34, VEGFR2, vWF and Dil-Ac-LDL engulfment, as well as the ability to form capillary-like structures. An in vitro study on the effect of hyperglycemia on the proliferation and viability of the cultured EPCs was also performed. RESULTS: The number of EPCs in type 2 diabetes was significantly decreased compared with healthy controls and there was an inverse correlation between the EPC numbers and plasma glucose, as well as HbA1(C). The number and function of EPCs in patients with good glycemic control were recovered compared with those with poor glycemic control. When glucose was supplemented in the culture in vitro, there was a negative effect on the proliferation and viability of EPCs, in a dose-dependent manner, whereas the enhancement of apoptosis was observed. CONCLUSION: There was EPC dysfunction in type 2 diabetes which might be improved by strict glycemic control. However, the circulating EPC number and proliferative function in patients with good glycemic control did not reach the level in healthy controls. BioMed Central 2010-04-07 /pmc/articles/PMC2858721/ /pubmed/20374643 http://dx.doi.org/10.1186/1472-6823-10-5 Text en Copyright ©2010 Churdchomjan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Churdchomjan, Worachat
Kheolamai, Pakpoom
Manochantr, Sirikul
Tapanadechopone, Pirath
Tantrawatpan, Chairat
U-pratya, Yaowalak
Issaragrisil, Surapol
Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control
title Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control
title_full Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control
title_fullStr Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control
title_full_unstemmed Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control
title_short Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control
title_sort comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858721/
https://www.ncbi.nlm.nih.gov/pubmed/20374643
http://dx.doi.org/10.1186/1472-6823-10-5
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