Human CC chemokine liver-expressed chemokine/CCL16 is a functional ligand for CCR1, CCR2 and CCR5, and constitutively expressed by hepatocytes

被引:81
作者
Nomiyama, H [1 ]
Hieshima, K
Nakayama, T
Sakaguchi, T
Fujisawa, R
Tanase, S
Nishiura, H
Matsuno, K
Takamori, H
Tabira, Y
Yamamoto, T
Miura, R
Yoshie, O
机构
[1] Kumamoto Univ, Sch Med, Dept Biochem, Kumamoto 8600811, Japan
[2] Kumamoto Univ, Sch Med, Dept Surg, Kumamoto 8600811, Japan
[3] Kumamoto Univ, Sch Med, Dept Mol Pathol, Kumamoto 8600811, Japan
[4] Kumamoto Univ, Sch Med, Dept Anat, Kumamoto 8600811, Japan
[5] Kinki Univ, Sch Med, Dept Microbiol, Osaka 5898511, Japan
关键词
chemokine; chemokine receptor; hepatocyte; HIV-1; plasma;
D O I
10.1093/intimm/13.8.1021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Liver-expressed chemokine (LEC)/CCL16 is a human CC chemokine selectively expressed in the liver. Here, we investigated its receptor usage by calcium mobilization and chemotactic assays using mouse L1.2 pre-B cell lines stably expressing a panel of 12 human chemokine receptors. At relatively high concentrations, LEG induced calcium mobilization and chemotaxis via CCR1 and CCR2. LEG also induced calcium mobilization, but marginal chemotaxis via CCR5. Consistently, LEG was found to bind to CCR1, CCR2 and CCR5 with relatively low affinities. The binding of LEG to CCR8 was much less significant. In spite of its binding to CCR5, LEG was unable to inhibit infection of an R5-type HIV-1 to activated human peripheral blood mononuclear cells even at high concentrations. In human liver sections, hepatocytes were strongly stained by anti-LEC antibody. HepG2, a human hepatocarcinoma cell line, was found to constitutively express LEC. LEG was also present in the plasma samples from healthy adult donors at relatively high concentrations (0.3-4 nM). Taken together, LEG is a new low-affinity functional ligand for CCR1, CCR2 and CCR5, and is constitutively expressed by liver parenchymal cells. The presence of LEG in normal plasma at relatively high concentrations may modulate inflammatory responses.
引用
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页码:1021 / 1029
页数:9
相关论文
共 38 条
[1]
Bernardini G, 1998, EUR J IMMUNOL, V28, P582, DOI 10.1002/(SICI)1521-4141(199802)28:02<582::AID-IMMU582>3.0.CO
[2]
2-A
[3]
Natural proteolytic processing of hemofiltrate CC chemokine 1 generates a potent CC chemokine receptor (CCR)1 and CCR5 agonist with anti-HIV properties [J].
Detheux, M ;
Ständker, L ;
Vakili, J ;
Münch, J ;
Forssmann, U ;
Adermann, K ;
Pöhlmann, S ;
Vassart, G ;
Kirchhoff, F ;
Parmentier, M ;
Forssmann, WG .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (10) :1501-1508
[4]
Genomic organization of the genes for human and mouse CC chemokine LEC [J].
Fukuda, S ;
Hanano, Y ;
Iio, M ;
Miura, R ;
Yoshie, O ;
Nomiyama, H .
DNA AND CELL BIOLOGY, 1999, 18 (04) :275-283
[5]
Garlisi CG, 1999, EUR J IMMUNOL, V29, P3210, DOI 10.1002/(SICI)1521-4141(199910)29:10<3210::AID-IMMU3210>3.0.CO
[6]
2-W
[7]
Tumor rejection and immune memory elicited by locally released LEC chemokine are associated with an impressive recruitment of APCs, lymphocytes, and granulocytes [J].
Giovarelli, M ;
Cappello, P ;
Forni, G ;
Salcedo, T ;
Moore, PA ;
LeFleur, DW ;
Nardelli, B ;
Di Carlo, E ;
Lollini, PL ;
Ruben, S ;
Ullrich, S ;
Garotta, G ;
Musiani, P .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :3200-3206
[8]
CX3C-chemokine, fractalkine-enhanced adhesion of THP-1 cells to endothelial cells through integrin-dependent and -independent mechanisms [J].
Goda, S ;
Imai, T ;
Yoshie, O ;
Yoneda, O ;
Inoue, H ;
Nagano, Y ;
Okazaki, T ;
Imai, H ;
Bloom, ET ;
Domae, N ;
Umehara, H .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :4313-4320
[9]
Characterization of a novel CC chemokine, HCC-4, whose expression is increased by interleukin-10 [J].
Hedrick, JA ;
Helms, A ;
Vicari, A ;
Zlotnik, A .
BLOOD, 1998, 91 (11) :4242-4247
[10]
Chemokine receptors and HIV-1: the fusion of two major research fields [J].
Horuk, R .
IMMUNOLOGY TODAY, 1999, 20 (02) :89-94