Expression of chemokine receptors CCR7 and CCR8 in the CNS during ChREAE

被引:20
作者
Bielecki, B. [1 ]
Mazurek, A. [1 ]
Wolinski, P. [1 ]
Glabinski, A. [1 ]
机构
[1] Med Univ Lodz, Dept Expt & Clin Neurol, PL-92215 Lodz, Poland
关键词
D O I
10.1111/j.1365-3083.2007.01954.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemokines and their receptors are important players in organism homeostasis, development and immune response to inflammatory stimuli. It has been recently confirmed that they are also involved in the development of several autoimmune diseases. In this study, we analysed the expression of two recently identified CC chemokine receptors, CCR7 and CCR8, in the central nervous system (CNS) and in peripheral tissues during chronic relapsing experimental autoimmune encephalomyelitis (ChREAE) - an animal model of the human demyelinating disease multiple sclerosis (MS). We observed upregulation of both chemokine receptors in the CNS during the first and second attacks of ChREAE, whereas disease remission was characterized by a lower expression of those receptors. An analysis of the kinetics of CCR7 and CCR8 expression in the CNS during the first attack of the disease showed a constant increase in the first few days after the onset of clinical signs. This expression correlated with the clinical severity of ChREAE. CCR7-positive mononuclear cells were detected mostly in perivascular inflammatory cuffs in the CNS. In peripheral tissues (the spleen and kidneys) expression of both receptors was not upregulated during active ChREAE. These findings suggest that CCR7 and CCR8 may play a significant role in the pathogenesis of EAE and probably MS.
引用
收藏
页码:383 / 392
页数:10
相关论文
共 68 条
[1]  
Alt C, 2002, EUR J IMMUNOL, V32, P2133, DOI 10.1002/1521-4141(200208)32:8<2133::AID-IMMU2133>3.0.CO
[2]  
2-W
[3]   CCR5+ and CXCR3+ T cells are increased in multiple sclerosis and their ligands MIP-1α and IP-10 are expressed in demyelinating brain lesions [J].
Balashov, KE ;
Rottman, JB ;
Weiner, HL ;
Hancock, WW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) :6873-6878
[4]   CC chemokine ligand 1 promotes recruitment of eosinophils but not Th2 cells during the development of allergic airways disease [J].
Bishop, B ;
Lloyd, CM .
JOURNAL OF IMMUNOLOGY, 2003, 170 (09) :4810-4817
[5]   CCR7 and CXCR4 as novel biomarkers predicting axillary lymph node metastasis in T1 breast cancer [J].
Cabioglu, N ;
Yazici, MS ;
Arun, B ;
Broglio, KR ;
Hortobagyi, GN ;
Price, JE ;
Sahin, A .
CLINICAL CANCER RESEARCH, 2005, 11 (16) :5686-5693
[6]  
Campbell JJ, 1999, J IMMUNOL, V163, P2353
[7]   Disparate lymphoid chemokine expression in mice and men: no evidence of CCL21 synthesis by human high endothelial venules [J].
Carlsen, HS ;
Haraldsen, G ;
Brandtzaeg, P ;
Baekkevold, ES .
BLOOD, 2005, 106 (02) :444-446
[8]   Focal interstitial CC chemokine receptor 7 (CCR7) expression in idiopathic interstitial pneumonia [J].
Choi, ES ;
Pierce, EM ;
Jakubzick, C ;
Carpenter, KJ ;
Kunkel, SL ;
Evanoff, H ;
Martinez, FJ ;
Flaherty, KR ;
Moore, BB ;
Toews, GB ;
Colby, TV ;
Kazerooni, EA ;
Gross, BH ;
Travis, WD ;
Hogaboam, CM .
JOURNAL OF CLINICAL PATHOLOGY, 2006, 59 (01) :28-39
[9]   The vast majority of CLA+ T cells are resident in normal skin [J].
Clark, Rachael A. ;
Chong, Benjamin ;
Mirchandani, Nina ;
Brinster, Nooshin K. ;
Yamanaka, Kei-ichi ;
Dowgiert, Rebecca K. ;
Kupper, Thomas S. .
JOURNAL OF IMMUNOLOGY, 2006, 176 (07) :4431-4439
[10]  
Columba-Cabezas S, 2003, BRAIN PATHOL, V13, P38