NKG2-C IS A RECEPTOR ON HUMAN NATURAL-KILLER-CELLS THAT RECOGNIZES STRUCTURES ON K562 TARGET-CELLS

被引:31
作者
DUCHLER, M
OFFTERDINGER, M
HOLZMULLER, H
LIPP, J
CHU, CT
ASCHAUER, B
BACH, FH
HOFER, E
机构
[1] VIENNA INT RES COOPERAT CTR, DEPT TRANSPLANTAT, A-1230 VIENNA, AUSTRIA
[2] HARVARD UNIV, NEW ENGLAND DEACONESS HOSP, SANDOZ CTR IMMUNOBIOL, BOSTON, MA 02215 USA
关键词
NATURAL KILLER CELL RECEPTORS; NKG2-C; K562 TARGET CELLS;
D O I
10.1002/eji.1830251032
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NKG2-C is a member of the recently discovered NKG2 family of genes and proteins, which are preferentially expressed on human natural killer (NK) cells. These potential NK cell receptors belong to a larger class of type II transmembrane proteins with a C-type lectin domain. We show here that NKG2-C is expressed as a 36-kDa glycoprotein by translation in vitro, recombinant expression and immunoprecipitation from a human NK cell clone. Further, a recombinant soluble NKG2-C-receptor binds specifically to K562 cells, which are target cells for NK cell killing, and to RPMI 8866 cells, which are feeder cells for NK cells; several other hematopoietic cell lines tested do not show any binding. The binding structures on the surface of K562 cells disappear, concomitant with a loss in susceptibility to killing when the cells are induced to differentiate with phorbol ester and Ca2+ ionophore. Our data suggest the presence of specific target molecules for NKG2-C on K562 cells, since overall glycosylation, Lewis X and Lewis Y structures, as well as the mucin-like CD43 molecule, do not change following induction of the cells. We propose that NKG2-C mediates a specific interaction of NK cells and their target cells with functional importance for NK cell killing.
引用
收藏
页码:2923 / 2931
页数:9
相关论文
共 56 条
  • [1] ADAMKIEWICZ TV, 1994, IMMUNOGENETICS, V39, P218
  • [2] ARAMBURU J, 1991, J IMMUNOL, V147, P714
  • [3] THE ROLE OF NATURAL-KILLER-CELLS IN INNATE RESISTANCE TO INFECTION
    BANCROFT, GJ
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1993, 5 (04) : 503 - 510
  • [4] BEZOUSKA K, 1994, J BIOL CHEM, V269, P16945
  • [5] RETRACTED: OLIGOSACCHARIDE LIGANDS FOR NKR-P1 PROTEIN ACTIVATE NK CELLS AND CYTOTOXICITY (Retracted article. See vol. 500, pg. 492, 2013)
    BEZOUSKA, K
    YUEN, CT
    OBRIEN, J
    CHILDS, RA
    CHAI, WG
    LAWSON, AM
    DRBAL, K
    FISEROVA, A
    POSPISIL, M
    FEIZI, T
    [J]. NATURE, 1994, 372 (6502) : 150 - 157
  • [6] THE HUMAN NATURAL-KILLER-CELL RECEPTOR FOR MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I MOLECULES - SURFACE MODULATION OF P58 MOLECULES AND THEIR LINKAGE TO CD3 ZETA-CHAIN, FC-EPSILON-RI GAMMA-CHAIN AND THE P56(LCK) KINASE
    BOTTINO, C
    VITALE, M
    OLCESE, L
    SIVORI, S
    MORELLI, L
    AUGUGLIARO, R
    CICCONE, E
    MORETTA, L
    MORETTA, A
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (10) : 2527 - 2534
  • [7] EXPRESSION OF DIFFERENT MEMBERS OF THE LY-49 GENE FAMILY DEFINES DISTINCT NATURAL-KILLER-CELL SUBSETS AND CELL-ADHESION PROPERTIES
    BRENNAN, J
    MAGER, D
    JEFFERIES, W
    TAKEI, F
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (06) : 2287 - 2295
  • [8] BRUNNER KT, 1968, IMMUNOLOGY, V14, P181
  • [9] MONOCLONAL-ANTIBODY TO A TRIGGERING STRUCTURE EXPRESSED ON RAT NATURAL-KILLER CELLS AND ADHERENT LYMPHOKINE-ACTIVATED KILLER CELLS
    CHAMBERS, WH
    VUJANOVIC, NL
    DELEO, AB
    OLSZOWY, MW
    HERBERMAN, RB
    HISERODT, JC
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (04) : 1373 - 1389
  • [10] CHAN PY, 1989, J IMMUNOL, V142, P1727