The effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells

The present study investigated the effects of glycated low density lipoprot ins (LDL) and lipoprotein(a) (Lp(a)) on the production of plasminogen activator inhibitor-1 (PAI-1) and tissue-type plasminogen activator (t-PA) from cultured human umbilical vein endothelial cells (HUVEC). The levels of PAI...

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Main Author: Zhang, Jianying
Format: Others
Language:en
en_US
Published: 2007
Online Access:http://hdl.handle.net/1993/1059
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-MWU.anitoba.ca-dspace#1993-10592013-01-11T13:31:43ZZhang, Jianying2007-05-15T15:27:30Z2007-05-15T15:27:30Z1997-04-01T00:00:00Zhttp://hdl.handle.net/1993/1059The present study investigated the effects of glycated low density lipoprot ins (LDL) and lipoprotein(a) (Lp(a)) on the production of plasminogen activator inhibitor-1 (PAI-1) and tissue-type plasminogen activator (t-PA) from cultured human umbilical vein endothelial cells (HUVEC). The levels of PAI-1 antigen were increased in the post-cultural media of HUVEC treated with native LDL or Lp(a) for 124 h. Glycation amplified the increase in PAI-1 secretion induced by native lipoproteins from HUVEC. A significant increase in PAI-1 generation was found in cultures treated with $\ge$50 $\mu$g/ml of glycated LDL or with 5 $\mu$g/ml of glycated Lp(a) for $\ge$24 h. The level of 2.4 kb PAI-1 mRNA in HUVEC treated with glycated LDL or Lp(a) was significantly increased and that was associated with moderate reduction of 3.4 kb PAI-1 mRNA level. The de novo synthesis and secretion of t-PA in HUVEC treated with 100 $\mu$g/ml of native LDL or with 5 $\mu$g/ml of native Lp(a) were reduced by incubation for $\ge$16 h. Treatment with $\ge$25 $\mu$g/ml of native LDL or $\ge$2.5 $\mu$g/ml of native Lp(a) for 24 h significantly reduced the secretion of t-PA from HUVEC compared to control cultures. Treatments with glycated LDL or Lp(a) further reduced the secretion and de novo synthesis of t-PA from HUVEC compared to native LDL and Lp(a). Treatment with $\ge$25 mM aminoguanidine, an inhibitor of the formation for advanced glycation end products (AGEs), during the glycation of lipoproteins normalized the generation of PAI-1 and t-PA from HUVEC induced by glycated lipoproteins. The results of the present study indicate that glycation enhances the production of PAI-1 and attenuates the synthesis of t-PA in vascular endothelial cells (EC) induced by native lipoproteins. (Abstract shortened by UMI.)4746170 bytes184 bytesapplication/pdftext/plainenen_USThe effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cellsPhysiologyM.Sc.
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language en
en_US
format Others
sources NDLTD
description The present study investigated the effects of glycated low density lipoprot ins (LDL) and lipoprotein(a) (Lp(a)) on the production of plasminogen activator inhibitor-1 (PAI-1) and tissue-type plasminogen activator (t-PA) from cultured human umbilical vein endothelial cells (HUVEC). The levels of PAI-1 antigen were increased in the post-cultural media of HUVEC treated with native LDL or Lp(a) for 124 h. Glycation amplified the increase in PAI-1 secretion induced by native lipoproteins from HUVEC. A significant increase in PAI-1 generation was found in cultures treated with $\ge$50 $\mu$g/ml of glycated LDL or with 5 $\mu$g/ml of glycated Lp(a) for $\ge$24 h. The level of 2.4 kb PAI-1 mRNA in HUVEC treated with glycated LDL or Lp(a) was significantly increased and that was associated with moderate reduction of 3.4 kb PAI-1 mRNA level. The de novo synthesis and secretion of t-PA in HUVEC treated with 100 $\mu$g/ml of native LDL or with 5 $\mu$g/ml of native Lp(a) were reduced by incubation for $\ge$16 h. Treatment with $\ge$25 $\mu$g/ml of native LDL or $\ge$2.5 $\mu$g/ml of native Lp(a) for 24 h significantly reduced the secretion of t-PA from HUVEC compared to control cultures. Treatments with glycated LDL or Lp(a) further reduced the secretion and de novo synthesis of t-PA from HUVEC compared to native LDL and Lp(a). Treatment with $\ge$25 mM aminoguanidine, an inhibitor of the formation for advanced glycation end products (AGEs), during the glycation of lipoproteins normalized the generation of PAI-1 and t-PA from HUVEC induced by glycated lipoproteins. The results of the present study indicate that glycation enhances the production of PAI-1 and attenuates the synthesis of t-PA in vascular endothelial cells (EC) induced by native lipoproteins. (Abstract shortened by UMI.)
author Zhang, Jianying
spellingShingle Zhang, Jianying
The effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells
author_facet Zhang, Jianying
author_sort Zhang, Jianying
title The effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells
title_short The effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells
title_full The effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells
title_fullStr The effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells
title_full_unstemmed The effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells
title_sort effects of glycated lipoproteins on production of fibrinolytic regulators in vascular endothelial cells
publishDate 2007
url http://hdl.handle.net/1993/1059
work_keys_str_mv AT zhangjianying theeffectsofglycatedlipoproteinsonproductionoffibrinolyticregulatorsinvascularendothelialcells
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