Stress Responses and Conditioning Effects in Mesothelial Cells Exposed to Peritoneal Dialysis Fluid

被引:23
作者
Kratochwill, Klaus [1 ]
Lechner, Michael [2 ]
Siehs, Christian [3 ]
Lederhuber, Hans C. [1 ]
Rehulka, Pavel [4 ]
Endemann, Michaela [1 ]
Kasper, David C. [1 ]
Herkner, Kurt R. [1 ]
Mayer, Bernd [3 ]
Rizzi, Andreas [2 ]
Aufricht, Christoph [1 ]
机构
[1] Med Univ Wien, Univ Klin F Kinder & Jugenheilkunde, Dept Pediat & Adolescent Med, A-1090 Vienna, Austria
[2] Univ Vienna, Inst Analyt Chem & Food Chem, A-1010 Vienna, Austria
[3] Emergentec Biodev GmbH, Vienna, Austria
[4] Acad Sci Czech Republ, Inst Analyt Chem, CS-61142 Brno, Czech Republic
基金
奥地利科学基金会;
关键词
HEAT-SHOCK PROTEINS; HIGH UREA CONCENTRATIONS; CIS-TRANS-ISOMERASES; MOLECULAR CHAPERONES; GENE-EXPRESSION; OSMOTIC-STRESS; IN-VITRO; PROTEOMICS; APOPTOSIS; KIDNEY;
D O I
10.1021/pr800916s
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Renal replacement therapy by peritoneal dialysis is frequently complicated by technical failure. Peritoneal dialysis fluids (PDF) cause injury to the peritoneal mesothelial cell layer due to their cytotoxicity. As only isolated elements of the involved cellular processes have been studied before, we aimed at a global assessment of the mesothelial stress response to PDF. Following single or repeated exposure to PDF or control medium, proteomics and bioinformatics techniques were combined to study effects in mesothelial cells (MeT-5A). Protein expression was assessed by two-dimensional gel electrophoresis, and significantly altered spots were identified by MALDI-TOF MS and MS2 techniques. The lists of experimentally derived candidate proteins were expanded by a next neighbor approach and analyzed for significantly enriched biological processes. To address the problem of an unknown portion of false positive spots in 2DGE, only proteins showing significant p-values on both levels were further interpreted. Single PDF exposure resulted in reduction of biological processes in favor of reparative responses, including protein metabolism, modification and folding, with chaperones as a major subgroup. The observed biological processes triggered by this acute PDF exposure mainly contained functionally interwoven multitasking proteins contributing as well to cytoskeletal reorganization and defense mechanisms. Repeated PDF exposure resulted in attenuated protein regulation, reflecting inhibition of stress responses by high levels of preincluced chaperones. The identified proteins were less attributable to acute cellular injury but rather to specialized functions with a reduced number of involved multitasking proteins. This finding agrees well with the concept of conditioning effects and cytoprotection. In conclusion, this study describes the reprogrammed proteome of mesothelial cells during recovery from PDF exposure and adaption to repetitive stress. A broad stress response with a number of highly overlapping processes and multitasking proteins shifts toward a more specific response of only few less overlapping processes.
引用
收藏
页码:1731 / 1747
页数:17
相关论文
共 50 条
[31]   The monocyte chemoattractant protein-1 (MCP-1)/CCR2 system is involved in peritoneal dialysis-related epithelial-mesenchymal transition of peritoneal mesothelial cells [J].
Lee, Sun Ha ;
Kang, Hye-Young ;
Kim, Kyung Sik ;
Nam, Bo Young ;
Paeng, Jisun ;
Kim, Seonghun ;
Li, Jin Ji ;
Park, Jung Tak ;
Kim, Dong Ki ;
Han, Seung Hyeok ;
Yoo, Tae-Hyun ;
Kang, Shin-Wook .
LABORATORY INVESTIGATION, 2012, 92 (12) :1698-1711
[32]   Effect of β-(3,4-Dihydroxyphenyl)Lactic Acid on Oxidative Stress Stimulated by High Glucose Levels in Human Peritoneal Mesothelial Cells [J].
Zhang, H. ;
Wang, J-W ;
Xu, Y. ;
Zhang, K. ;
Yi, B. ;
Sun, J. ;
Liu, Y. ;
Zhang, X-M ;
Liu, J-S .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2012, 40 (03) :943-953
[33]   Endothelial Cells Exposed to Fluid Shear Stress Support Diffusion Based Maturation of Adult Neural Progenitor Cells [J].
Dumont, C. M. ;
Piselli, J. ;
Temple, S. ;
Dai, G. ;
Thompson, D. M. .
CELLULAR AND MOLECULAR BIOENGINEERING, 2018, 11 (02) :117-130
[34]   Autophagy caused by oxidative stress promotes TGF-β1-induced epithelial-to-mesenchymal transition in human peritoneal mesothelial cells [J].
Oh, Se-Hyun ;
Yook, Ju-Min ;
Jung, Hee-Yeon ;
Choi, Ji-Young ;
Cho, Jang-Hee ;
Park, Sun-Hee ;
Kim, Chan-Duck ;
Kim, Yong-Lim ;
Lim, Jeong-Hoon .
CELL DEATH & DISEASE, 2024, 15 (05)
[35]   CYTOTOXICITY OF MONONUCLEAR CELLS AS INDUCED BY PERITONEAL DIALYSIS FLUIDS: INSIGHT INTO MECHANISMS THAT REGULATE OSMOTIC STRESS-RELATED APOPTOSIS [J].
Gastaldello, Karine ;
Husson, Cecile ;
Dondeyne, Jean-Paul ;
Vanherweghem, Jean-Louis ;
Tielemans, Christian .
PERITONEAL DIALYSIS INTERNATIONAL, 2008, 28 (06) :655-666
[36]   The effects of fluid shear stress on proliferation and osteogenesis of human periodontal ligament cells [J].
Zheng, Lisha ;
Chen, Luoping ;
Chen, Yuchao ;
Gui, Jinpeng ;
Li, Qing ;
Huang, Yan ;
Liu, Meili ;
Jia, Xiaolin ;
Song, Wei ;
Ji, Jing ;
Gong, Xianghui ;
Shi, Ruoshi ;
Fan, Yubo .
JOURNAL OF BIOMECHANICS, 2016, 49 (04) :572-579
[37]   Effects of Fluid Shear Stress on a Distinct Population of Vascular Smooth Muscle Cells [J].
Hsu, Steven ;
Chu, Julia S. ;
Chen, Fanqing F. ;
Wang, Aijun ;
Li, Song .
CELLULAR AND MOLECULAR BIOENGINEERING, 2011, 4 (04) :627-636
[38]   Fluid Shear Stress Pre-Conditioning Promotes Endothelial Morphogenesis of Embryonic Stem Cells Within Embryoid Bodies [J].
Nsiah, Barbara A. ;
Ahsan, Tabassum ;
Griffiths, Sarah ;
Cooke, Marissa ;
Nerem, Robert M. ;
McDevitt, Todd C. .
TISSUE ENGINEERING PART A, 2014, 20 (5-6) :954-965
[39]   Protective Effects of Transforming Growth Factor β2 in Intestinal Epithelial Cells by Regulation of Proteins Associated with Stress and Endotoxin Responses [J].
Duc Ninh Nguyen ;
Jiang, Pingping ;
Jacobsen, Susanne ;
Sangild, Per T. ;
Bendixen, Emoke ;
Chatterton, Dereck E. W. .
PLOS ONE, 2015, 10 (02)
[40]   Effects of Astragaloside IV Against the TGF-β1-Induced Epithelial-to-Mesenchymal Transition in Peritoneal Mesothelial Cells by Promoting Smad 7 Expression [J].
Zhang, Lu ;
Li, Zhenghong ;
He, Weinning ;
Xu, Lingdong ;
Wang, Jing ;
Shi, Jun ;
Sheng, Meixiao .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2015, 37 (01) :43-54