Cross-Omics Comparison of Stress Responses in Mesothelial Cells Exposed to Heat- versus Filter-Sterilized Peritoneal Dialysis Fluids

被引:3
|
作者
Kratochwill, Klaus [1 ,2 ]
Bender, Thorsten O. [1 ,3 ]
Lichtenauer, AntonM. [1 ,2 ]
Herzog, Rebecca [1 ,2 ]
Tarantino, Silvia [1 ]
Bialas, Katarzyna [2 ]
Joerres, Achim [3 ]
Aufricht, Christoph [1 ]
机构
[1] Med Univ Vienna, Dept Pediat & Adolescent Med, A-1090 Vienna, Austria
[2] Zytoprotec GmbH, A-1090 Vienna, Austria
[3] Charite, Dept Nephrol & Med Intens Care, Campus Virchow Klinikum, D-13353 Berlin, Germany
关键词
GLUCOSE DEGRADATION-PRODUCTS; CIS-TRANS-ISOMERASES; OXIDATIVE STRESS; PROTEIN; GLUCOSE-6-PHOSPHATE-DEHYDROGENASE; EXPRESSION; IMPAIRS; CALCINEURIN; CULTURE;
D O I
10.1155/2015/628158
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Recent research suggests that cytoprotective responses, such as expression of heat-shock proteins, might be inadequately induced in mesothelial cells by heat-sterilized peritoneal dialysis (PD) fluids. This study compares transcriptome data and multiple protein expression profiles for providing new insight into regulatory mechanisms. Two-dimensional difference gel electrophoresis (2D-DIGE) based proteomics and topic defined gene expression microarray-based transcriptomics techniques were used to evaluate stress responses in human omental peritoneal mesothelial cells in response to heat-or filter-sterilized PD fluids. Data from selected heat-shock proteins were validated by 2D western-blot analysis. Comparison of proteomics and transcriptomics data discriminated differentially regulated protein abundance into groups depending on correlating or noncorrelating transcripts. Inadequate abundance of several heat-shock proteins following exposure to heat-sterilized PD fluids is not reflected on the mRNA level indicating interference beyond transcriptional regulation. For the first time, this study describes evidence for posttranscriptional inadequacy of heat-shock protein expression by heat-sterilized PD fluids as a novel cytotoxic property. Crossomics technologies introduce a novel way of understanding PDF bioincompatibility and searching for new interventions to reestablish adequate cytoprotective responses.
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页数:12
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