NKp44, a triggering receptor involved in tumor cell lysis by activated human natural killer cells, is a novel member of the immunoglobulin superfamily

被引:367
作者
Cantoni, C
Bottino, C
Vitale, M
Pessino, A
Augugliaro, R
Malaspina, A
Parolini, S
Moretta, L
Moretta, A
Biassoni, R
机构
[1] Ctr Biotechnol Avanzate, Lab Immunopatol, I-16132 Genoa, Italy
[2] Ist Nazl Ric Canc, I-16132 Genoa, Italy
[3] Univ Genoa, Dipartimento Med Sperimentale, I-16132 Genoa, Italy
[4] Univ Brescia, Dipartimento Sci Biomed & Biotecnol, I-25100 Brescia, Italy
关键词
natural killer cells; activating receptor; natural cytotoxicity; immunoglobulin superfamily; cDNA;
D O I
10.1084/jem.189.5.787
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
Surface receptors involved in natural killer (NK) cell triggering during the process of tumor cell lysis have recently been identified. Of these receptors, NKp44 is selectively expressed by IL-2-activated NK cells and may contribute to the increased efficiency of activated. NK cells to mediate tumor cell lysis, Here we describe the molecular cloning of NKp44. Analysis of the cloned cDNA indicated that NKp44 is a novel transmembrane glycoprotein belonging to the Immunoglobulin superfamily characterized by a single extracellular V-type domain. The charged amino acid lysine in the transmembrane region may be involved in the association of NKp44 with the signal transducing molecule killer activating receptor-associated polypeptide (KARAP)/DAP12. These molecules were found to be crucial for the surface expression of NKp44. In agreement with data of NKp44 surface expression, the NKp44 transcripts were strictly confined to activated NK cells and to a minor subset of TCR-gamma/delta(+) T lymphocytes. Unlike genes coding for other receptors involved in NK cell triggering or inhibition, the NKp44 gene is on human chromosome 6.
引用
收藏
页码:787 / 795
页数:9
相关论文
共 27 条
[1]
BIASSONI R, 1988, J IMMUNOL, V140, P1685
[2]
Borges L, 1997, J IMMUNOL, V159, P5192
[3]
THE HUMAN E48 ANTIGEN, HIGHLY HOMOLOGOUS TO THE MURINE LY-6 ANTIGEN THB, IS A GPI-ANCHORED MOLECULE APPARENTLY INVOLVED IN KERATINOCYTE CELL-CELL ADHESION [J].
BRAKENHOFF, RH ;
GERRETSEN, M ;
KNIPPELS, EMC ;
VANDIJK, M ;
VANESSEN, H ;
WEGHUIS, DO ;
SINKE, RJ ;
SNOW, GB ;
VANDONGEN, GAMS .
JOURNAL OF CELL BIOLOGY, 1995, 129 (06) :1677-1689
[4]
TRANSCRIPTION OF THE DYSTROPHIN GENE IN HUMAN-MUSCLE AND NON-MUSCLE TISSUES [J].
CHELLY, J ;
KAPLAN, JC ;
MAIRE, P ;
GAUTRON, S ;
KAHN, A .
NATURE, 1988, 333 (6176) :858-860
[5]
FERRINI S, 1987, J IMMUNOL, V138, P1297
[6]
LYMPHOKINE-ACTIVATED KILLER CELL PHENOMENON - LYSIS OF NATURAL KILLER-RESISTANT FRESH SOLID TUMOR-CELLS BY INTERLEUKIN 2-ACTIVATED AUTOLOGOUS HUMAN PERIPHERAL-BLOOD LYMPHOCYTES [J].
GRIMM, EA ;
MAZUMDER, A ;
ZHANG, HZ ;
ROSENBERG, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (06) :1823-1841
[7]
PREDICTION OF O-GLYCOSYLATION OF MAMMALIAN PROTEINS - SPECIFICITY PATTERNS OF UDP-GALNAC-POLYPEPTIDE N-ACETYLGALACTOSAMINYLTRANSFERASE [J].
HANSEN, JE ;
LUND, O ;
ENGELBRECHT, J ;
BOHR, H ;
NIELSEN, JO ;
HANSEN, JES ;
BRUNAK, S .
BIOCHEMICAL JOURNAL, 1995, 308 :801-813
[8]
MOLECULAR-CLONING OF A NOVEL MEMBER OF THE IMMUNOGLOBULIN GENE SUPERFAMILY HOMOLOGOUS TO THE POLYMERIC IMMUNOGLOBULIN RECEPTOR [J].
JACKSON, DG ;
HART, DNJ ;
STARLING, G ;
BELL, JI .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (05) :1157-1163
[9]
WHY ARE PROTEINS O-GLYCOSYLATED [J].
JENTOFT, N .
TRENDS IN BIOCHEMICAL SCIENCES, 1990, 15 (08) :291-294
[10]
SPECIFIC RECRUITMENT OF SH-PTP1 TO THE ERYTHROPOIETIN RECEPTOR CAUSES INACTIVATION OF JAK2 AND TERMINATION OF PROLIFERATIVE SIGNALS [J].
KLINGMULLER, U ;
LORENZ, U ;
CANTLEY, LC ;
NEEL, BG ;
LODISH, HF .
CELL, 1995, 80 (05) :729-738