Involvement of CC chemokine ligand 18 (CCL18) in normal and pathological processes

被引:229
作者
Schutyser, E
Richmond, A
Van Damme, J
机构
[1] Katholieke Univ Leuven, Lab Mol Immunol, Rega Inst Med Res, B-3000 Louvain, Belgium
[2] Vanderbilt Univ, Sch Med, Dept Vet Affairs, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Canc Biol, Nashville, TN 37212 USA
关键词
dendritic cells; macrophages; chemotaxis; inflammatory; homing;
D O I
10.1189/jlb.1204712
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CC chemokine ligand 18 (CCL18) was originally discovered as pulmonary and activation-regulated chemokine (PARC), dendritic cell (DC)-chemokine 1 (DC-CK1), alternative macrophage activation-associated CC chemokine-1 (AMAC-1), and macrophage inflammatory protein-4 (MIP-4). CCL18 primarily targets lymphocytes and immature DC, although its agonistic receptor remains unknown so far. CCL18 is mainly expressed by a broad range of monocytes/macrophages and DC. A more profound understanding of the various activation programs and functional phenotypes of these producer cells might give a better insight in the proinflammatory versus anti-inflammatory role of this CC chemokine. It is interesting that CCL18 is constitutively present at high levels in human plasma and likely contributes to the physiological homing of lymphocytes and DC and to the generation of primary immune responses. Furthermore, enhanced CCL18 production has been demonstrated in several diseases, including various malignancies and inflammatory joint, lung, and skin diseases. The lack of a rodent counterpart for human CCL18 sets all hope on primate animal models to further elucidate the importance of CCL18 in vivo. This review will address these different aspects in more detail.
引用
收藏
页码:14 / 26
页数:13
相关论文
共 95 条
[1]   Expression of T lymphocyte chemoattractants and activation markers in vernal keratoconjunctivitis [J].
Abu El-Asrar, AM ;
Struyf, S ;
Al-Kharashi, SA ;
Missotten, L ;
Van Damme, J ;
Geboes, K .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2002, 86 (10) :1175-1180
[2]   A dendritic-cell-derived C-C chemokine that preferentially attracts naive T cells [J].
Adema, GJ ;
Hartgers, F ;
Verstraten, R ;
deVries, E ;
Marland, G ;
Menon, S ;
Foster, J ;
Xu, YM ;
Nooyen, P ;
McClanahan, T ;
Bacon, KB ;
Figdor, CG .
NATURE, 1997, 387 (6634) :713-717
[3]   Pulmonary and activation-regulated chemokine stimulates collagen production in lung fibroblasts [J].
Atamas, SP ;
Luzina, IG ;
Choi, J ;
Tsymbalyuk, N ;
Carbonetti, NH ;
Singh, IS ;
Trojanowska, M ;
Jimenez, SA ;
White, B .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2003, 29 (06) :743-749
[4]   Molecular cloning and sequencing of 25 different rhesus macaque chemokine cDNAs reveals evolutionary conservation among C, CC, CXC, and CX3C families of chemokines [J].
Basu, S ;
Schaefer, TM ;
Ghosh, M ;
Fuller, CL ;
Reinhart, TA .
CYTOKINE, 2002, 18 (03) :140-148
[5]  
BERKMAN N, 1995, J IMMUNOL, V155, P4412
[6]   Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention [J].
Boot, RG ;
Verhoek, M ;
de Fost, M ;
Hollak, CEM ;
Maas, M ;
Bleijlevens, B ;
van Breemen, MJ ;
van Meurs, M ;
Boven, LA ;
Laman, JD ;
Moran, MT ;
Cox, TM ;
Aerts, JMFG .
BLOOD, 2004, 103 (01) :33-39
[7]  
BORXMEYER HE, 1999, ANN NY ACAD SCI, V872, P142
[8]   Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophages [J].
Boven, LA ;
van Meurs, M ;
Boot, RG ;
Mehta, A ;
Boon, L ;
Aerts, JM ;
Laman, JD .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2004, 122 (03) :359-369
[9]   The β-thromboglobulins and platelet factor 4:: blood platelet-derived CXC chemokines with divergent roles in early neutrophil regulation [J].
Brandt, E ;
Petersen, F ;
Ludwig, A ;
Ehlert, JE ;
Bock, L ;
Flad, HD .
JOURNAL OF LEUKOCYTE BIOLOGY, 2000, 67 (04) :471-478
[10]   Generation of functional human dendritic cells from adherent peripheral blood monocytes by CD40 ligation in the absence of granulocyte-macrophage colony-stimulating factor [J].
Brossart, P ;
Grünebach, F ;
Stuhler, G ;
Reichardt, VL ;
Möhle, R ;
Kanz, L ;
Brugger, WR .
BLOOD, 1998, 92 (11) :4238-4247