Peritoneal dialysate fluid composition determines heat shock protein expression patterns in human mesothelial cells

Peritoneal dialysate fluid composition determines heat shock protein expression patterns in human mesothelial cells. Low biocompatibility of peritoneal dialysis fluids (PDF) contributes to mesothelial injury. We investigated whether the heat shock proteins (HSP)-27, HSP-72, and HSP-90 are differenti...

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Veröffentlicht in:Kidney international 2001-11, Vol.60 (5), p.1930-1937
Hauptverfasser: Arbeiter, Klaus, Bidmon, Bettina, Endemann, Michaela, Bender, Thorsten Onno, Eickelberg, Oliver, Ruffingshofer, Dagmar, Mueller, Thomas, Regele, Heinz, Herkner, Kurt, Aufricht, Christoph
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container_end_page 1937
container_issue 5
container_start_page 1930
container_title Kidney international
container_volume 60
creator Arbeiter, Klaus
Bidmon, Bettina
Endemann, Michaela
Bender, Thorsten Onno
Eickelberg, Oliver
Ruffingshofer, Dagmar
Mueller, Thomas
Regele, Heinz
Herkner, Kurt
Aufricht, Christoph
description Peritoneal dialysate fluid composition determines heat shock protein expression patterns in human mesothelial cells. Low biocompatibility of peritoneal dialysis fluids (PDF) contributes to mesothelial injury. We investigated whether the heat shock proteins (HSP)-27, HSP-72, and HSP-90 are differentially induced upon exposure of mesothelial cells to PDF and whether this was affected by selective modulation of the physicochemical properties of PDF. Human mesothelial cells (Met5A and primary human mesothelial cells) were exposed to acidic lactate and glucose-monomer based PDF (CAPD2 and CAPD3), to control culture media, or to a neutral lactate and glucose-monomer-based PDF with reduced levels of glucose degradation products (BALANCE). Expression of HSP-27, HSP-72, and HSP-90 and cellular distribution of HSP-72 were assessed by Western blotting and immunocytochemistry. Mesothelial cells exhibited strong constitutive expression of HSP-27 and to a lesser extent HSP-72 and HSP-90. Exposure of the cells to CAPD2 and CAPD3 resulted in strong up-regulation of HSP-72. HSP-27 levels were slightly increased, but HSP-90 levels were unchanged upon exposure to CAPD2 or CAPD3. In contrast, exposure of the cells to BALANCE did not affect HSP-27 or HSP-72 expression. The acidic pH and glucose degradation products were found to be principal in mediating increased HSP-72 expression upon exposure to PDF. Analysis of HSP expression represents a novel tool to assess biocompatibility of PDF. Among the HSP investigated, HSP-72 is the most predictive and accurate parameter to assess mesothelial cell injury in the early phase of exposure to PDF.
doi_str_mv 10.1046/j.1523-1755.2001.00004.x
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Low biocompatibility of peritoneal dialysis fluids (PDF) contributes to mesothelial injury. We investigated whether the heat shock proteins (HSP)-27, HSP-72, and HSP-90 are differentially induced upon exposure of mesothelial cells to PDF and whether this was affected by selective modulation of the physicochemical properties of PDF. Human mesothelial cells (Met5A and primary human mesothelial cells) were exposed to acidic lactate and glucose-monomer based PDF (CAPD2 and CAPD3), to control culture media, or to a neutral lactate and glucose-monomer-based PDF with reduced levels of glucose degradation products (BALANCE). Expression of HSP-27, HSP-72, and HSP-90 and cellular distribution of HSP-72 were assessed by Western blotting and immunocytochemistry. Mesothelial cells exhibited strong constitutive expression of HSP-27 and to a lesser extent HSP-72 and HSP-90. Exposure of the cells to CAPD2 and CAPD3 resulted in strong up-regulation of HSP-72. 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Low biocompatibility of peritoneal dialysis fluids (PDF) contributes to mesothelial injury. We investigated whether the heat shock proteins (HSP)-27, HSP-72, and HSP-90 are differentially induced upon exposure of mesothelial cells to PDF and whether this was affected by selective modulation of the physicochemical properties of PDF. Human mesothelial cells (Met5A and primary human mesothelial cells) were exposed to acidic lactate and glucose-monomer based PDF (CAPD2 and CAPD3), to control culture media, or to a neutral lactate and glucose-monomer-based PDF with reduced levels of glucose degradation products (BALANCE). Expression of HSP-27, HSP-72, and HSP-90 and cellular distribution of HSP-72 were assessed by Western blotting and immunocytochemistry. Mesothelial cells exhibited strong constitutive expression of HSP-27 and to a lesser extent HSP-72 and HSP-90. Exposure of the cells to CAPD2 and CAPD3 resulted in strong up-regulation of HSP-72. HSP-27 levels were slightly increased, but HSP-90 levels were unchanged upon exposure to CAPD2 or CAPD3. In contrast, exposure of the cells to BALANCE did not affect HSP-27 or HSP-72 expression. The acidic pH and glucose degradation products were found to be principal in mediating increased HSP-72 expression upon exposure to PDF. Analysis of HSP expression represents a novel tool to assess biocompatibility of PDF. Among the HSP investigated, HSP-72 is the most predictive and accurate parameter to assess mesothelial cell injury in the early phase of exposure to PDF.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>11703612</pmid><doi>10.1046/j.1523-1755.2001.00004.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
biocompatibility
Biological and medical sciences
cell injury
Cells, Cultured
cytotoxicity
Dialysis Solutions - chemistry
Emergency and intensive care: renal failure. Dialysis management
Epithelial Cells - metabolism
glucose degradation
Heat-Shock Proteins - biosynthesis
HSP72 Heat-Shock Proteins
HSP90 Heat-Shock Proteins - biosynthesis
Humans
Intensive care medicine
Medical sciences
Peritoneal Dialysis
stress response
ultrafiltration
title Peritoneal dialysate fluid composition determines heat shock protein expression patterns in human mesothelial cells
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