Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular Cells
Erythropoietin (EPO) exerts (renal) tissue protective effects. Since it is unclear whether this is a direct effect of EPO on the kidney or not, we investigated whether EPO is able to protect human renal tubular epithelial cells (hTECs) from oxidative stress and if so which pathways are involved. EPO...
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doaj-24a0837b7c3c4dd79997fafa9f73233d2020-11-25T00:53:35ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512010-01-01201010.1155/2010/395785395785Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular CellsAnnelies De Beuf0Xiang-hua Hou1Patrick C. D'Haese2Anja Verhulst3Laboratory of Pathophysiology, Faculties of Medicine and Biomedical, Pharmaceutical and Veterinary Sciences, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, BelgiumLaboratory of Pathophysiology, Faculties of Medicine and Biomedical, Pharmaceutical and Veterinary Sciences, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, BelgiumLaboratory of Pathophysiology, Faculties of Medicine and Biomedical, Pharmaceutical and Veterinary Sciences, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, BelgiumLaboratory of Pathophysiology, Faculties of Medicine and Biomedical, Pharmaceutical and Veterinary Sciences, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, BelgiumErythropoietin (EPO) exerts (renal) tissue protective effects. Since it is unclear whether this is a direct effect of EPO on the kidney or not, we investigated whether EPO is able to protect human renal tubular epithelial cells (hTECs) from oxidative stress and if so which pathways are involved. EPO (epoetin delta) could protect hTECs against oxidative stress by a dose-dependent inhibition of reactive oxygen species formation. This protective effect is possibly related to the membranous expression of the EPO receptor (EPOR) since our data point to the membranous EPOR expression as a prerequisite for this protective effect. Oxidative stress reduction went along with the upregulation of renoprotective genes. Whilst three of these, heme oxygenase-1 (HO-1), aquaporin-1 (AQP-1), and B-cell CLL/lymphoma 2 (Bcl-2) have already been associated with EPO-induced renoprotection, this study for the first time suggests carboxypeptidase M (CPM), dipeptidyl peptidase IV (DPPIV), and cytoglobin (Cygb) to play a role in this process.http://dx.doi.org/10.1155/2010/395785 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Annelies De Beuf Xiang-hua Hou Patrick C. D'Haese Anja Verhulst |
spellingShingle |
Annelies De Beuf Xiang-hua Hou Patrick C. D'Haese Anja Verhulst Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular Cells Journal of Biomedicine and Biotechnology |
author_facet |
Annelies De Beuf Xiang-hua Hou Patrick C. D'Haese Anja Verhulst |
author_sort |
Annelies De Beuf |
title |
Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular Cells |
title_short |
Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular Cells |
title_full |
Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular Cells |
title_fullStr |
Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular Cells |
title_full_unstemmed |
Epoetin Delta Reduces Oxidative Stress in Primary Human Renal Tubular Cells |
title_sort |
epoetin delta reduces oxidative stress in primary human renal tubular cells |
publisher |
Hindawi Limited |
series |
Journal of Biomedicine and Biotechnology |
issn |
1110-7243 1110-7251 |
publishDate |
2010-01-01 |
description |
Erythropoietin (EPO) exerts (renal) tissue protective effects. Since it is unclear whether this is a direct effect of EPO on the kidney or not, we investigated whether EPO is able to protect human renal tubular epithelial cells (hTECs) from oxidative stress and if so which pathways are involved. EPO (epoetin delta) could protect hTECs against oxidative stress by a dose-dependent inhibition of reactive oxygen species formation. This protective effect is possibly related to the membranous expression of the EPO receptor (EPOR) since our data point to the membranous EPOR expression as a prerequisite for this protective effect. Oxidative stress reduction went along with the upregulation of renoprotective genes. Whilst three of these, heme oxygenase-1 (HO-1), aquaporin-1 (AQP-1), and B-cell CLL/lymphoma 2 (Bcl-2) have already been associated with EPO-induced renoprotection, this study for the first time suggests carboxypeptidase M (CPM), dipeptidyl peptidase IV (DPPIV), and cytoglobin (Cygb) to play a role in this process. |
url |
http://dx.doi.org/10.1155/2010/395785 |
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