2011•Zhongguo bingli shengli zazhiRequires access

Effects of high glucose on proliferation,migration,adhesion and secretion of rat late endothelial progenitor cells

Min Cheng

Open publisher page 0 citations

Abstract

AIM: To investigate the effects of high glucose on the proliferation,adhesion,migration and secretion potentials of late endothelial progenitor cells(EPCs) from bone marrow.METHODS: Mononuclear cells were collected from rat bone marrow by density gradient centrifugation and cultured with M199 medium.The early EPCs were identified by DiI-ac-LDL and FITC-UEA-1 double staining.The late EPCs were identified by RT-PCR to detect the expression of von Willebrand factor(vWF) and VE-cadherin.Moreover,the cells were identified by FACS to detect the expression of CD133 and vascular endothelial growth factor receptor-2(VEGFR-2).The 3rd generation of EPCs was harvested and incubated with glucose in a series of concentrations(5,10,20 or 40 mmol/L).The cell proliferation,adhesion,migration and the secretion of chemokines such as monocyte chemoattractant protein-1(MCP-1) and interleukin-8(IL-8) were assayed with MTT,adhesion test,modified Boyden chamber assay and ELISA,respectively.RESULTS: Compared with normal glucose(5 mmol/L)treatment,high glucose(10,20,40 mmol/L) dose-dependently degraded the proliferation and migration of late EPCs(P0.05 or P0.01).At the same time,treatment with glucose at the concentration of 40 mmol/L decreased the adhesion of EPCs(P0.05) and increased the release of MCP-1 and IL-8 by late EPCs.CONCLUSION: High glucose inhibits proliferation,adhesion and migration of late EPCs,and enhances the secretion of inflammatory factors,indicating that the high glucose correlates with the vascular complications of patients with diabetes.

About this research paper

What this paper is about

AIM: To investigate the effects of high glucose on the proliferation,adhesion,migration and secretion potentials of late endothelial progenitor cells(EPCs) from bone marrow.METHODS: Mononuclear cells were collected from rat bone marrow by density gradient centrifugation and cultured with M199 medium.The early EPCs were identified by DiI-ac-LDL and FITC-UEA-1 double staining.The late EPCs were identified by RT-PCR to detect the expression of von Willebrand factor(vWF) and VE-cadherin.Moreover,the cells were identified by FACS to detect the expression of CD133 and vascular endothelial growth factor receptor-2(VEGFR-2).The 3rd generation of EPCs was harvested and incubated with glucose in a series of concentrations(5,10,20 or 40 mmol/L).The cell proliferation,adhesion,migration and the secretion of chemokines such as monocyte chemoattractant protein-1(MCP-1) and interleukin-8(IL-8) were assayed with MTT,adhesion test,modified Boyden chamber assay and ELISA,respectively.RESULTS: Compared with normal glucose(5 mmol/L)treatment,high glucose(10,20,40 mmol/L) dose-dependently degraded the proliferation and migration of late EPCs(P0.05 or P0.01).At the same time,treatment with glucose at the concentration of 40 mmol/L decreased the adhesion of EPCs(P0.05) and increased the release of MCP-1 and IL-8 by late EPCs.CONCLUSION: High glucose inhibits proliferation,adhesion and migration of late EPCs,and enhances the secretion of inflammatory factors,indicating that the high glucose correlates with the vascular complications of patients with diabetes.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

AIM: To investigate the effects of high glucose on the proliferation,adhesion,migration and secretion potentials of late endothelial progenitor cells(EPCs) from bone marrow.METHODS: Mononuclear cells were collected from rat bone marrow by density gradient centrifugation and cultured with M199 medium.The early EPCs were identified by DiI-ac-LDL and FITC-UEA-1 double staining.The late EPCs were identified by RT-PCR to detect the expression of von Willebrand factor(vWF) and VE-cadherin.Moreover,the cells were identified by FACS to detect the expression of CD133 and vascular endothelial growth factor receptor-2(VEGFR-2).The 3rd generation of EPCs was harvested and incubated with glucose in a series of concentrations(5,10,20 or 40 mmol/L).The cell proliferation,adhesion,migration and the secretion of chemokines such as monocyte chemoattractant protein-1(MCP-1) and interleukin-8(IL-8) were assayed with MTT,adhesion test,modified Boyden chamber assay and ELISA,respectively.RESULTS: Compared with normal glucose(5 mmol/L)treatment,high glucose(10,20,40 mmol/L) dose-dependently degraded the proliferation and migration of late EPCs(P0.05 or P0.01).At the same time,treatment with glucose at the concentration of 40 mmol/L decreased the adhesion of EPCs(P0.05) and increased the release of MCP-1 and IL-8 by late EPCs.CONCLUSION: High glucose inhibits proliferation,adhesion and migration of late EPCs,and enhances the secretion of inflammatory factors,indicating that the high glucose correlates with the vascular complications of patients with diabetes.

Key concepts: Progenitor cell, Internal medicine, Chemokine, Bone marrow, Endocrinology, Endothelial progenitor cell, Differential centrifugation, Peripheral blood mononuclear cell

Related papers

Back to paper searchBrowse research topicsOriginal source
Effects of high glucose on proliferation,migration,adhesion and secretion of rat late endothelial progenitor cells — Research Paper | ScholarLens