Expression of the DNAM-1 ligands, Nectin-2 (CD112) and poliovirus receptor (CD155), on dendritic cells: relevance for natural killer-dendritic cell interaction

被引:210
作者
Pende, D
Castriconi, R
Romagnani, P
Spaggiari, GM
Marcenaro, S
Dondero, A
Lazzeri, E
Lasagni, L
Martini, S
Rivera, P
Capobianco, A
Moretta, L
Moretta, A
Bottino, C
机构
[1] Ist Nazl Ric Canc, I-16132 Genoa, Italy
[2] Univ Genoa, Dipartimento Med Sperimentale, Genoa, Italy
[3] Ist Giannina Gaslini, Genoa, Italy
[4] Univ Florence, Ctr Res Transfer & High Educ De Nono Therapies, Florence, Italy
[5] Univ Genoa, Ctr Eccellenza Ric Biomed, Genoa, Italy
[6] Univ Genoa, Dipartimento Oncol Biol & Genet, I-16126 Genoa, Italy
关键词
D O I
10.1182/blood-2005-07-2696
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study, we demonstrate the involvement of DNAM-1-triggering receptor and its ligands, poliovirus receptor (PVR) and Nectin-2, in natural killer (NK) cell-mediated lysis of dendritic cells (DCs). The surface expression of both ligands was up-regulated in DCs as compared to monocytes. It reached maximal densities after DC maturation induced by different stimuli including lipopolysaccharide (LPS), poly I:C, flagellin, and CD40L. Both immunohistochemical analysis and confocal microscopy revealed expression of DNAM-1 ligands by DCs in lymph nodes in which they were localized in the parafollicular T-cell region and surrounded the high endothelial venules. Remarkably, in cytolytic assays, DNAM-1 cooperated with NKp30 in the NK-mediated killing of both immature and mature DCs and the degree of contribution of DNAM-1 appeared to correlate with the surface densities of its specific ligands PVR and Nectin-2.
引用
收藏
页码:2030 / 2036
页数:7
相关论文
共 42 条
[41]   KIR: Diverse, rapidly evolving receptors of innate and adaptive immunity [J].
Vilches, C ;
Parham, P .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :217-251
[42]   NK-dependent DC maturation is mediated by TNFα and IFNγ released upon engagement of the NKp30 triggering receptor [J].
Vitale, M ;
Della Chiesa, M ;
Carlomagno, S ;
Pende, D ;
Aricò, M ;
Moretta, L ;
Moretta, A .
BLOOD, 2005, 106 (02) :566-571