Literature DB >> 21193553

Peritoneal dialysis fluid induces p38-dependent inflammation in human mesothelial cells.

Andrea Riesenhuber1, Klaus Kratochwill, Thorsten O Bender, Regina Vargha, David C Kasper, Rebecca Herzog, Elisabeth Salzer, Christoph Aufricht.   

Abstract

BACKGROUND: Noninfectious upregulation of proinflammatory pathways in mesothelial cells may represent an integral part of their stress response upon exposure to peritoneal dialysis fluids (PDF).
OBJECTIVE: The aim of this study was to evaluate the role of the stress-inducible mitogen-activated protein kinase (MAPK) p38 in regulation of inflammatory and stress responses in mesothelial cells following in vitro exposure to PDF.
MATERIALS AND METHODS: Human peritoneal mesothelial cells were exposed to Dianeal PD4 or Physioneal (Baxter AG, Vienna, Austria) containing 1.36% glucose and then allowed to recover. Phosphorylation of p38, induction of heat shock protein-70 (HSP70), release of lactate dehydrogenase (LDH), secretion of interleukin (IL)-8, gene transcription, and mRNA stability were assessed with and without the MAPK p38 inhibitor SB203580.
RESULTS: Exposure to Dianeal resulted in phosphorylation of p38 within 30 minutes (309% of control, p < 0.05) and increased IL-8 release (370% of control, p < 0.05), HSP70 expression (151% of control, p < 0.05), and LDH release (180% of control, p < 0.05). Exposure to Physioneal resulted in attenuated changes in IL-8, HSP70, and LDH. Addition of the p38 inhibitor SB203580 to Dianeal resulted in dampened IL-8 release (-55%; p < 0.05) and basal HSP70 expression, and unchanged LDH release. Effects of p38 on IL-8 were at transcriptional, posttranscriptional, and translational levels.
CONCLUSION: These data confirm concordant p38-dependent upregulation of IL-8 and HSP70 following exposure to bioincompatible PDF. The MAPK p38 pathway therefore links proinflammatory processes and the cellular stress response in human peritoneal mesothelial cells.

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Year:  2010        PMID: 21193553     DOI: 10.3747/pdi.2009.00206

Source DB:  PubMed          Journal:  Perit Dial Int        ISSN: 0896-8608            Impact factor:   1.756


  3 in total

1.  PPAR-γ agonist rosiglitazone ameliorates peritoneal deterioration in peritoneal dialysis rats with LPS-induced peritonitis through up-regulation of AQP-1 and ZO-1.

Authors:  Yunfang Zhang; Junxia Feng; Qi Wang; Shili Zhao; Jiaqi Xu; Hongyan Li
Journal:  Biosci Rep       Date:  2018-06-21       Impact factor: 3.840

2.  Activation of General Control Nonderepressible-2 Kinase Ameliorates Glucotoxicity in Human Peritoneal Mesothelial Cells, Preserves Their Integrity, and Prevents Mesothelial to Mesenchymal Transition.

Authors:  Theodoros Eleftheriadis; Georgios Pissas; Georgia Antoniadi; Evdokia Nikolaou; Spyridon Golfinopoulos; Vassilios Liakopoulos; Ioannis Stefanidis
Journal:  Biomolecules       Date:  2019-12-05

3.  Bacterial infection elicits heat shock protein 72 release from pleural mesothelial cells.

Authors:  Julius F Varano Della Vergiliana; Sally M Lansley; Jose M Porcel; Silvia Bielsa; Jeremy S Brown; Jenette Creaney; Suzanna E L Temple; Grant W Waterer; Y C Gary Lee
Journal:  PLoS One       Date:  2013-05-21       Impact factor: 3.240

  3 in total

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