Correlation between HSP-72 expression and IL-8 secretion in human mesothelial cells

被引:15
作者
Bender, T. O.
Riesenhuber, A.
Endemann, M.
Herkner, K.
Witowski, J.
Joerres, A.
Aufricht, C.
机构
[1] Med Univ, Dept Pediat, Vienna, Austria
[2] Univ Klinikum Berlin, Charite, Dept Nephrol & Med Intens Care, Berlin, Germany
关键词
peritoneal dialysis; HSP-72; IL-8; HPMC; heat shock response; PERITONEAL-DIALYSIS FLUIDS; IN-VITRO; INDUCE;
D O I
10.1177/039139880703000304
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: Cytotoxicity of peritoneal dialysis fluid (PDF) and peritoneal inflammation are currently regarded as the two major culprits for chronic mesothelial injury and peritoneal membrane failure. In this study, we correlated induction of HSP-72, as a marker of the cellular stress response, to secretion of IL-8, as a marker for pro-inflammatory cytokines, in mesothelial cells upon sublethal PDF exposure. Methods: Primary omental cell cultures of human mesothelial cells were subjected to sublethal PDF exposure times (CAPD2, Fresenius, Germany). At the end of a 24 hour recovery period, induction of HSP-72 in the cell homogenate and IL-8 secretion in the supernatant was assessed by immunodensitometry and ELISA, respectively. Results: PDF exposure times from 15 min to 60 min resulted in progressively increased HSP-72 expression levels (267 vs 320 vs 419% of controls, p<0.05 vs controls) as well as increased IL-8 secretion (323 vs 528 vs 549% of controls, p<0.05 vs controls) with full cell viability (MTT unchanged to control). HSP-72 expression was statistically significantly correlated with IL-8 secretion. Conclusions: The significant correlation between HSP-72 expression and IL-8 secretion suggests that the regulation of pro-inflammatory pathways in mesothelial cells exposed to PDF may represent an integral part of their stress response. Future studies to investigate the cellular regulatory mechanism involved are warranted.
引用
收藏
页码:199 / 203
页数:5
相关论文
共 18 条
[1]   Peritoneal dialysate fluid composition determines heat shock protein expression patterns in human mesothelial cells [J].
Arbeiter, K ;
Bidmon, B ;
Endemann, M ;
Bender, TO ;
Eickelberg, O ;
Ruffingshofer, D ;
Mueller, T ;
Regele, H ;
Herkner, K ;
Aufricht, C .
KIDNEY INTERNATIONAL, 2001, 60 (05) :1930-1937
[2]  
ARBEITER K, 2003, PERITON DIALYSIS INT, V23, P1
[3]   HSP: Helper, suppressor, protector [J].
Aufricht, C .
KIDNEY INTERNATIONAL, 2004, 65 (02) :739-740
[4]  
Aufricht C, 2001, PERITON DIALYSIS INT, V21, P85
[5]   Effect of glucose concentration, osmolality, and sterilization process of peritoneal dialysis fluids on cytokine production by peripheral blood mononuclear cells and polymorphonuclear cell functions in vitro [J].
Cendoroglo, M ;
Sundaram, S ;
Jaber, BL ;
Pereira, BJG .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (02) :273-282
[6]   What really happens to people on long-term peritoneal dialysis? [J].
Davies, SJ ;
Phillips, L ;
Griffiths, AM ;
Russell, LH ;
Naish, PF ;
Russell, GI .
KIDNEY INTERNATIONAL, 1998, 54 (06) :2207-2217
[7]   Many forms of renal injury induce a stereotyped response with increased expression of MHC, IFN-gamma, and adhesion molecules [J].
Goes, N ;
Hobart, M ;
Ramassar, V ;
Urmson, J ;
Halloran, PF .
TRANSPLANTATION PROCEEDINGS, 1997, 29 (1-2) :1085-1085
[8]   Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases [J].
Johnson, GL ;
Lapadat, R .
SCIENCE, 2002, 298 (5600) :1911-1912
[9]   Early loss of proliferative potential of human peritoneal mesothelial cells in culture:: the role of p16INK4a-mediated premature senescence [J].
Ksiazek, K ;
Piwocka, K ;
Brzezinska, A ;
Sikora, E ;
Zabel, M ;
Breborowicz, A ;
Jörres, A ;
Witowski, J .
JOURNAL OF APPLIED PHYSIOLOGY, 2006, 100 (03) :988-995
[10]   Expression of heat shock proteins 72/73 in human peritoneal mesothelial cells in vivo and in vitro [J].
López-Cotarelo, C ;
Sellhaus, B ;
Baba, HA ;
Manegold, E ;
Luka, J ;
Handt, S ;
Mittermayer, C ;
Klosterhalfen, B ;
Tietze, L .
NEPHRON, 2000, 85 (02) :148-155