The chemokine receptor CXCR7 is expressed on lymphatic endothelial cells during renal allograft rejection

被引:31
|
作者
Neusser, Matthias A. [1 ,2 ]
Kraus, Anna K. [1 ]
Regele, Heinz [3 ]
Cohen, Clemens D. [1 ,4 ]
Fehr, Thomas [1 ]
Kerjaschki, Dontscho [3 ]
Wuethrich, Rudolf P. [1 ]
Penfold, Mark E. T. [5 ]
Schall, Thomas [5 ]
Segerer, Stephan [1 ,6 ]
机构
[1] Univ Zurich Hosp, Div Nephrol, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Dept Internal Med, CH-8091 Zurich, Switzerland
[3] Univ Vienna, Clin Inst Pathol, Vienna, Austria
[4] Univ Zurich, Inst Physiol, Zurich Ctr Integrat Human Physiol, Zurich, Switzerland
[5] ChemoCentryx, Mountain View, CA USA
[6] Univ Zurich, Inst Anat, Zurich, Switzerland
关键词
chemokines; CXCL12; CXCR7; lymphatic endothelial cell; renal allograft; GENE-EXPRESSION; NEOANGIOGENESIS; RDC1; CXCL12/SDF-1; MIGRATION; PROTOCOL; LIGAND; TISSUE; CXCL11; SDF-1;
D O I
10.1038/ki.2010.6
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
CXCR7 is an atypical receptor for the chemokines CXCL11 and CXCL12, which were found to be involved in animal models of allograft injury. We studied the expression of CXCR7 and its ligands in human kidneys by first quantifying the mRNA in 53 renal allograft biopsies. Receptor and ligand mRNAs were expressed in renal allografts, with a significant induction of CXCL11 and CXCL12 in biopsies showing borderline lesions and acute rejection. Immunohistochemical analysis for CXCR7 was performed in a series of 64 indication and 24 protocol biopsies. The indication biopsies included 46 acute rejections, 6 with interstitial fibrosis and tubular atrophy, and 12 pretransplant biopsies as controls. In control biopsies, CXCR7 protein was found on smooth muscle and on endothelial cells of a small number of peritubular vessels. The number of CXCR7-positive vessels was increased in acute rejection and, using double immunofluorescence labeling, a subset of these CXCR7-positive endothelial cells were identified as lymphatic vessels. Both CXCR7-positive blood and lymphatic vessels increased during allograft rejection. We found that CXCR7 is present in both blood and lymphatic endothelial cells in human renal allografts. Whether its presence modulates the formation of chemokine gradients and the recruitment of inflammatory cells will require further experimental studies. Kidney International (2010) 77, 801-808; doi: 10.1038/ki.2010.6; published online 17 February 2010
引用
收藏
页码:801 / 808
页数:8
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