NDLI: Proteomics analysis identifies PARK7 as an important player for renal cell resistance and survival under oxidative stress

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Eltoweissy, Marwa Müller, Gerhard A. Bibi, Asima Nguye, Phuc Van Dihazi, Gry H. Müller, Claudia A. Dihazi, Hassan
Description	Country affiliation: Germany Author Affiliation: Eltoweissy M ( Department of Nephrology and Rheumatology, University Medical Center Goettingen, Georg-August University Goettingen, Robert-Koch-Strasse 40, D-37075 Goettingen, Germany. dihazi@med.uni-goettingen.de)
Abstract	Renal fibrosis is a process that is characterized by declining excretory renal function. The molecular mechanisms of fibrosis are not fully understood. Oxidative stress pathways were reported to be involved in renal tissue deterioration and fibrosis progression. In order to identify new molecular targets associated with oxidative stress and renal fibrosis, differential proteomics analysis was performed with established renal cell lines (TK173 and HK-2). The cells were treated with oxidative stress triggering factor $H_{2}O_{2}$ and the proteome alterations were investigated. Two dimensional protein maps were generated and differentially expressed proteins were processed and identified using mass spectrometry analysis combined with data base search. Interestingly the increase of ROS in the renal cell lines upon $H_{2}O_{2}$ treatment was accompanied by alteration of a large number of proteins , which could be classified in three categories: the first category grouped the proteins that have been described to be involved in fibrogenesis (e.g.ACTA2, VIN, VIM, DES, KRT, COL1A1, COL4A1), the second category, which was more interesting involved proteins of the oxidative stress pathway (PRDX1, PRDX2, PRDX6, SOD, PARK7, HYOU1), which were highly up-regulated under oxidative stress, and the third category represented proteins , which are involved in different other metabolic pathways. Among the oxidative stress proteins the up-regulation of PARK7 was accompanied by a shift in the pI as a result of oxidation . Knockdown of PARK7 using siRNA led to significant reduction in renal cell viability under oxidative stress. Under $H_{2}O_{2}$ treatment the PARK7 knockdown cells showed up to 80% decrease in cell viability and an increase in apoptosis compared to the controls. These results highlight for the first time the important role of PARK7 in oxidative stress resistance in renal cells.
File Format	HTM / HTML
ISSN	1742206X
Issue Number	4
Volume Number	7
e-ISSN	17422051
Journal	Molecular BioSystems
Language	English
Publisher	Royal Society of Chemistry
Publisher Date	2011-04-01
Publisher Place	Great Britain (UK)
Access Restriction	Subscribed
Subject Keyword	Discipline Molecular Biology Discipline Biochemistry Intracellular Signaling Peptides And Proteins Metabolism Kidney Physiopathology Oncogene Proteins Oxidative Stress Proteomics Cell Line Cell Survival Drug Effects Fibroblasts Humans Hydrogen Peroxide Pharmacology Rna Interference Rna, Small Interfering Genetics Reactive Oxygen Species Journal Article
Content Type	Text
Resource Type	Article
Subject	Molecular Biology Biotechnology

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