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Title:Improved protective effect of umbilical cord stem cell transplantation on cisplatin-induced kidney injury in mice pretreated with antithymocyte globulin
Authors:ID Večerić-Haler, Željka (Author)
ID Erman, Andreja (Author)
ID Cerar, Anton (Author)
ID Motaln, Helena (Author)
ID Kološa, Katja (Author)
ID Lah Turnšek, Tamara (Author)
ID Sodin-Šemrl, Snežna (Author)
ID Lakota, Katja (Author)
ID Mrak Poljšak, Katjuša (Author)
ID Škrajnar, Špela (Author)
ID Kranjc Brezar, Simona (Author)
ID Arnol, Miha (Author)
ID Perše, Martina (Author)
Files:URL URL - Source URL, visit http://dx.doi.org/10.1155/2016/3585362
 
.pdf PDF - Presentation file, download (9,54 MB)
MD5: 4B034231D577409C86A19ED670B93287
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Logo OI - Institute of Oncology
Abstract:Mesenchymal stem cells (MSCs) are recognised as a promising tool to improve renal recovery in experimental models of cisplatin-induced acute kidney injury. However, these preclinical studies were performed on severely immunodeficient animals. Here, we investigated whether human umbilical cord derived MSC treatment could equally ameliorate acute kidney injury induced by cisplatin and prolong survival in mice with a normal immune system and those with a suppressed immune system by polyclonal antithymocyte globulin (ATG). We demonstrated that ATG pretreatment, when followed by MSC transplantation, significantly improved injured renal function parameters, as evidenced by decreased blood urea nitrogen and serum creatinine concentration, as well as improved renal morphology. This tissue restoration was also supported by increased survival of mice. The beneficial effects of ATG were associated with reduced level of inflammatory protein serum amyloid A3 and induced antioxidative expression of superoxide dismutase-1 (SOD-1), glutathione peroxidase (GPx), and hem oxygenase-1 (HO-1). Infused MSCs became localised predominantly in peritubular areas and acted to reduce renal cell death. In conclusion, these results show that ATG diminished in situ inflammation and oxidative stress associated with cisplatin-induced acute kidney injury, the effects that may provide more favourable microenvironment for MSC action, with consequential synergistic improvements in renal injury and animal survival as compared to MSC treatment alone.
Keywords:mesenchymal stem cells, nephrotoxicity
Publication status:Published
Publication version:Version of Record
Publication date:01.06.2016
Year of publishing:2016
Number of pages:str. 1-12
Numbering:Vol. 2016
PID:20.500.12556/DiRROS-19709 New window
UDC:577.2
ISSN on article:1687-9678
DOI:10.1155/2016/3585362 New window
COBISS.SI-ID:3713871 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 7. 1. 2016;
Publication date in DiRROS:25.07.2024
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Downloads:0
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Record is a part of a journal

Title:Stem Cells International (Online)
Shortened title:stem cells int.
Publisher:Hindawi Publishing Corporation
ISSN:1687-9678
COBISS.SI-ID:518503961 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0054-2014
Name:Patologija in molekularna genetika

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0108-2014
Name:Diferenciacija urotelijskih celic

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0323-2013
Name:Ledvične bolezni in nadomestna zdravljenja

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0245-2015
Name:Ekotoksiologija, toksikološka genomika in karcinogeneza

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0314-2015
Name:Sistemske avtoimunske bolezni

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

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