Filtration of Macrophage Migration Inhibitory Factor (MIF) in Patients with End Stage Renal Disease Undergoing Hemodialysis

被引:7
作者
Luedike, Peter [1 ]
Rammos, Christos [1 ]
Pohl, Julia [1 ]
Heisler, Martin [1 ]
Totzeck, Matthias [1 ]
Kleophas, Werner [2 ]
Hetzel, Gerd R. [2 ]
Kelm, Malte [1 ]
Hendgen-Cotta, Ulrike [1 ]
Rassaf, Tienush [1 ]
机构
[1] Univ Hosp Dusseldorf, Fac Med, Div Cardiol Pulmonol & Vasc Med, D-40225 Dusseldorf, Germany
[2] DaVita Renal Ctr, D-40210 Dusseldorf, Germany
关键词
CHRONIC KIDNEY-DISEASE; CARDIOVASCULAR OUTCOMES; OXIDATIVE STRESS; DYSFUNCTION; EXPRESSION; CHEMOKINE; INFLAMMATION; ACTIVATION; PLATELETS; SECRETION;
D O I
10.1371/journal.pone.0140215
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background End stage renal disease (ESRD) patients are characterized by increased morbidity and mortality due to highest prevalence of cardiovascular disease. Macrophage migration inhibitory factor (MIF) is an inflammatory cytokine that controls cellular signaling in human physiology, pathophysiology, and diseases. Increased MIF plasma levels promote vascular inflammation and development of atherosclerosis. We have shown that MIF is associated with vascular dysfunction in ESRD patients. Whether hemodialysis (HD) affects circulating MIF plasma levels is unknown. We here aimed to investigate whether HD influences the circulating MIF pool in ESRD patients. Methods and Results An observational single-center study was conducted. MIF plasma levels in ESRD patients were assessed before, during, and after a HD session (n = 29). Healthy age-matched volunteers served as controls to compare correlations of MIF plasma levels with inflammatory plasma components (n = 20). MIF removed from the circulating blood pool could be detected in the dialysate and allowed for calculation of totally removed MIF (MIF content in dialysate 219 +/- 4 mu g/HD-session). MIF plasma levels were markedly decreased 2 hour after initiation of HD (MIF plasma level pre-HD 84.8 +/- 6 ng/ml to intra-HD 61.2 +/- 5 ng/ml p<0.001) and were replenished already 20 min after termination of HD to basal levels (intra-HD 61.2 +/- 5 ng/ml to post-HD 79.8 +/- 5 ng/ml, p<0.001). Conclusion MIF is a dialyzable plasma component that is effectively filtrated during HD from the patient blood pool in large amounts. After removal of remarkable amounts of MIF during a single HD session, MIF plasma pool is early reconstituted after termination of HD from unknown sources.
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页数:13
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共 31 条
[1]  
Anavekar NS, 2004, NEW ENGL J MED, V351, P1285, DOI 10.1056/NEJMoa041365
[2]   Regulation of the immune response by macrophage migration inhibitory factor: biological and structural features [J].
Bernhagen, J ;
Calandra, T ;
Bucala, R .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1998, 76 (3-4) :151-161
[3]   MIF is a noncognate ligand of CXC chemokine receptors in inflammatory and atherogenic cell recruitment [J].
Bernhagen, Juergen ;
Krohn, Regina ;
Lue, Hongqi ;
Gregory, Julia L. ;
Zernecke, Alma ;
Koenen, Rory R. ;
Dewor, Manfred ;
Georgiev, Ivan ;
Schober, Andreas ;
Leng, Lin ;
Kooistra, Teake ;
Fingerle-Rowson, Guenter ;
Ghezzi, Pietro ;
Kleemann, Robert ;
McColl, Shaun R. ;
Bucala, Richard ;
Hickey, Michael J. ;
Weber, Christian .
NATURE MEDICINE, 2007, 13 (05) :587-596
[4]   Expression of macrophage migration inhibitory factor in different stages of human atherosclerosis [J].
Burger-Kentischer, A ;
Goebel, H ;
Seder, R ;
Fraedrich, G ;
Schaefer, HE ;
Dimmeler, S ;
Kleemann, R ;
Bernhagen, J ;
Ihling, C .
CIRCULATION, 2002, 105 (13) :1561-1566
[5]   Macrophage Migration Inhibitory Factor Limits Activation-Induced Apoptosis of Platelets via CXCR7-Dependent Akt Signaling [J].
Chatterjee, Madhumita ;
Borst, Oliver ;
Walker, Britta ;
Fotinos, Anna ;
Vogel, Sebastian ;
Seizer, Peter ;
Mack, Andreas ;
Alampour-Rajabi, Setareh ;
Rath, Dominik ;
Geisler, Tobias ;
Lang, Florian ;
Langer, Harald F. ;
Bernhagen, Juergen ;
Gawaz, Meinrad .
CIRCULATION RESEARCH, 2014, 115 (11) :939-+
[6]   Experience with the GENIUS® hemodialysis system [J].
Fassbinder, W .
KIDNEY & BLOOD PRESSURE RESEARCH, 2003, 26 (02) :96-99
[7]   Inflammation and oxidative stress in end-stage renal disease patients treated with hemodialysis or peritoneal dialysis [J].
Filiopoulos, Vassilis ;
Hadjiyannakos, Dimitrios ;
Takouli, Lambrini ;
Metaxaki, Polixeni ;
Sideris, Vasilis ;
Vlassopoulos, Dimosthenis .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 2009, 32 (12) :872-882
[8]   Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization [J].
Go, AS ;
Chertow, GM ;
Fan, DJ ;
McCulloch, CE ;
Hsu, CY .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (13) :1296-1305
[9]   Chronic kidney disease is associated with increased platelet activation and poor response to antiplatelet therapy [J].
Gremmel, Thomas ;
Mueller, Markus ;
Steiner, Sabine ;
Seidinger, Daniela ;
Koppensteiner, Renate ;
Kopp, Christoph W. ;
Panzer, Simon .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2013, 28 (08) :2116-2122
[10]   Cardioprotection Through S-Nitros(yl)ation of Macrophage Migration Inhibitory Factor [J].
Luedike, Peter ;
Hendgen-Cotta, Ulrike B. ;
Sobierajski, Julia ;
Totzeck, Matthias ;
Reeh, Marcel ;
Dewor, Manfred ;
Lue, Hongqi ;
Krisp, Christoph ;
Wolters, Dirk ;
Kelm, Malte ;
Bernhagen, Juergen ;
Rassaf, Tienush .
CIRCULATION, 2012, 125 (15) :1880-+