Efficient Renal Recruitment of Macrophages and T Cells in Mice Lacking the Duffy Antigen/Receptor for Chemokines

被引:31
|
作者
Vielhauer, Volker [2 ]
Allam, Ramanjaneyulu [2 ]
Lindenmeyer, Maja T. [1 ,3 ,4 ]
Cohen, Clemens D. [1 ,3 ,4 ]
Draganovici, Dan [2 ]
Mandelbaum, Jana [2 ]
Eltrich, Nuru [2 ]
Nelson, Peter J. [2 ]
Anders, Hans-Joachim [2 ]
Pruenster, Monika [6 ]
Rot, Antal [6 ]
Schloedorff, Detlef [7 ]
Segerer, Stephan [1 ,2 ,5 ]
机构
[1] Univ Zurich Hosp, Div Nephrol, CH-8091 Zurich, Switzerland
[2] Univ Munich, Med Poliklin, D-8000 Munich, Germany
[3] Univ Zurich, Inst Physiol, Zurich, Switzerland
[4] Univ Zurich, Ctr Integrat Human Physiol, Zurich, Switzerland
[5] Univ Zurich, Inst Anat, Zurich, Switzerland
[6] Novartis Inst BioMed Res, Vienna, Austria
[7] Mt Sinai Sch Med, New York, NY USA
来源
AMERICAN JOURNAL OF PATHOLOGY | 2009年 / 175卷 / 01期
关键词
CRESCENTIC GLOMERULONEPHRITIS; INTERSTITIAL INFLAMMATION; PROGRESSIVE FIBROSIS; TRANSPLANT REJECTION; ENDOTHELIAL-CELLS; LEUKOCYTE SUBSETS; ANTIGEN RECEPTOR; EXPRESSION; DARC; BLOCKADE;
D O I
10.2353/ajpath.2009.080590
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The Duffy antigen/receptor for chemokines (DARC) is a chemokine-binding protein that is expressed on erythrocytes and renal endothelial cells. DARC-mediated endothelial transcytosis of chemokines may facilitate the renal recruitment of macrophages and T cells, as has been suggested for neutrophils. We studied the role of Darc in two mouse models of prolonged renal inflammation, one that primarily involves the tubulointerstitium (unilateral ureteral obstruction), and one that requires an adaptive immune response that leads to glomerulonephritis (accelerated nephrotoxic nephritis). Renal expression of Darc and its ligands was increased in both models. Leukocytes effectively infiltrated obstructed kidneys in Darc-deficient mice with pronounced T-cell infiltration at early time points. Development of interstitial fibrosis was comparable in both genotypes. Nephrotoxic nephritis was inducible in Darc-deficient mice, with both an increased humoral immune response and functional impairment during the early phase of disease. Lecukocytes efficiently infiltrated kidneys of Darc-deficient mice, with increased cell numbers at early but not late time points. Taken together, renal inflammation developed more rapidly in DARC-deficient mice, without affecting the extent of renal injury at later time points. Thus, genetic elimination of Darc in mice does not prevent the development of renal infiltrates and may even enhance such development during the early phases of interstitial and glomerular diseases in mouse models of prolonged renal inflammation. (Am J Pathol 2009, 175:119-131; DOI: 10.2353/ajpath.2009.080590)
引用
收藏
页码:119 / 131
页数:13
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