Cutting edge: NTB-A activates NK cells via homophilic interaction

被引:67
作者
Flaig, RM [1 ]
Stark, S [1 ]
Watzl, C [1 ]
机构
[1] Univ Heidelberg, Inst Immunol, D-69120 Heidelberg, Germany
关键词
D O I
10.4049/jimmunol.172.11.6524
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NK cells are an important component of the innate immune system. Their activity is tightly regulated by activating and inhibitory surface receptors. However, the exact functions of many activating surface receptors, as well as their ligands, still remain to be elucidated. NTB-A is a receptor on the surfaces of human NK, T, and B cells, mediating a signal whose malfunction may be involved in X-linked lymphoproliferative disease. However, the ligand of NTB-A has remained elusive so far. Using trimeric recombinant proteins, we now show that NTB-A is its own ligand. Homophilic interaction of NTB- A enhances NK cell cytotoxicity and influences NK cell proliferation and IFN-gamma secretion. We suggest that NTB-A is an interlymphocyte signaling molecule, which serves to orchestrate the activities of immune cells.
引用
收藏
页码:6524 / 6527
页数:4
相关论文
共 27 条
[1]   Natural killer cells in antiviral defense: Function and regulation by innate cytokines [J].
Biron, CA ;
Nguyen, KB ;
Pien, GC ;
Cousens, LP ;
Salazar-Mather, TP .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :189-220
[2]   GNTB-A, a novel SH2D1A-associated surface molecule contributing to the inability of natural killer cells to kill Epstein-Barr-virus-infected B cells in X-linked lymphoproliferative disease [J].
Bottino, C ;
Falco, M ;
Parolini, S ;
Marcenaro, E ;
Augugliaro, R ;
Sivori, S ;
Landi, E ;
Biassoni, R ;
Notarangelo, LD ;
Moretta, L ;
Moretta, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (03) :235-246
[3]   2B4, the natural killer and T cell immunoglobulin superfamily surface protein, is a ligand for CD48 [J].
Brown, MH ;
Boles, K ;
van der Merwe, PA ;
Kumar, V ;
Mathew, PA ;
Barclay, AN .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (11) :2083-2090
[4]   The SAP and SLAM families in immune responses and X-linked lymphoproliferative disease [J].
Pablo Engel ;
Michael J. Eck ;
Cox Terhorst .
Nature Reviews Immunology, 2003, 3 (10) :813-821
[5]   Identification and characterization of SF2000 and SF2001, two new members of the immune receptor SLAM/CD2 family [J].
Fraser, CC ;
Howie, D ;
Morra, M ;
Qiu, YB ;
Murphy, C ;
Shen, Q ;
Gutierrez-Ramos, JC ;
Coyle, A ;
Kingsbury, GA ;
Terhorst, C .
IMMUNOGENETICS, 2002, 53 (10-11) :843-850
[6]   CRYSTAL-STRUCTURE OF AN ISOLEUCINE-ZIPPER TRIMER [J].
HARBURY, PB ;
KIM, PS ;
ALBER, T .
NATURE, 1994, 371 (6492) :80-83
[7]   CD48 IS A COUNTER-RECEPTOR FOR MOUSE CD2 AND IS INVOLVED IN T-CELL ACTIVATION [J].
KATO, K ;
KOYANAGI, M ;
OKADA, H ;
TAKANASHI, T ;
WONG, YW ;
WILLIAMS, AF ;
OKUMURA, K ;
YAGITA, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (05) :1241-1249
[8]   PHYSICAL AND GENETIC-LINKAGE OF THE GENES ENCODING LY-9 AND CD48 ON MOUSE AND HUMAN-CHROMOSOMES-1 [J].
KINGSMORE, SF ;
SOURYAL, CA ;
WATSON, ML ;
PATEL, DD ;
SELDIN, MF .
IMMUNOGENETICS, 1995, 42 (01) :59-62
[9]   CS1, a novel member of the CD2 family, is homophilic and regulates NK cell function [J].
Kumaresan, PR ;
Lai, WC ;
Chuang, SS ;
Bennett, M ;
Mathew, PA .
MOLECULAR IMMUNOLOGY, 2002, 39 (1-2) :1-8
[10]   Natural killer cell receptor signaling [J].
Lanier, LL .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (03) :308-314