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Apoptosis signal-regulating kinase 1 promotes Ochratoxin A-induced renal cytotoxicity.
- Source :
-
Scientific reports [Sci Rep] 2015 Jan 28; Vol. 5, pp. 8078. Date of Electronic Publication: 2015 Jan 28. - Publication Year :
- 2015
-
Abstract
- Oxidative stress and apoptosis are involved in Ochratoxin A (OTA)-induced renal cytotoxicity. Apoptosis signal-regulating kinase 1 (ASK1) is a Mitogen-Activated Protein Kinase Kinase Kinase (MAPKKK, MAP3K) family member that plays an important role in oxidative stress-induced cell apoptosis. In this study, we performed RNA interference of ASK1 in HEK293 cells and employed an iTRAQ-based quantitative proteomics approach to globally investigate the regulatory mechanism of ASK1 in OTA-induced renal cytotoxicity. Our results showed that ASK1 knockdown alleviated OTA-induced ROS generation and Δψm loss and thus desensitized the cells to OTA-induced apoptosis. We identified 33 and 24 differentially expressed proteins upon OTA treatment in scrambled and ASK1 knockdown cells, respectively. Pathway classification and analysis revealed that ASK1 participated in OTA-induced inhibition of mRNA splicing, nucleotide metabolism, the cell cycle, DNA repair, and the activation of lipid metabolism. We concluded that ASK1 plays an essential role in promoting OTA-induced renal cytotoxicity.
- Subjects :
- Chromatography, High Pressure Liquid
Gene Expression Regulation drug effects
HEK293 Cells
Humans
Kidney metabolism
MAP Kinase Kinase Kinase 5 antagonists & inhibitors
MAP Kinase Kinase Kinase 5 genetics
Membrane Potential, Mitochondrial drug effects
Oxidative Stress drug effects
Proteome analysis
Proteome drug effects
RNA Interference
RNA Splicing drug effects
RNA, Small Interfering metabolism
Reactive Oxygen Species metabolism
Tandem Mass Spectrometry
Apoptosis drug effects
Kidney drug effects
MAP Kinase Kinase Kinase 5 metabolism
Ochratoxins toxicity
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 5
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 25627963
- Full Text :
- https://doi.org/10.1038/srep08078