Molecular clones of the p58 NK cell receptor reveal immunoglobulin-related molecules with diversity in both the extra- and intracellular domains.

Recognition of major histocompatibility class I molecules on target cells by natural killer (NK) cells confers selective protection from NK-mediated lysis. Cross-linking of the p58 NK receptor, involved in the recognition of HLA-C alleles, delivers a negative signal that prevents target cell lysis. Molecular cloning of the p58 NK receptor reported here revealed a new member of the immunoglobulin superfamily. Five distinct p58 receptors, with sequence diversity in the immunoglobulin-related domains, were identified in a single individual. All NK clones tested expressed at least one p58 member. Three different types of transmembrane and cytoplasmic domains exist, even among receptors with closely related extracellular domains. These data revealed a repertoire of NK cells with clonally distributed p58 receptors exhibiting diversity in both extracellular and intracellular domains.

[1]  P. Parham,et al.  Specificity of HLA class I antigen recognition by human NK clones: evidence for clonal heterogeneity, protection by self and non-self alleles, and influence of the target cell type , 1993, The Journal of experimental medicine.

[2]  Eric O Long,et al.  Efficient cDNA expression vectors for stable and transient expression of HLA-DR in transfected fibroblast and lymphoid cells. , 1991, Human immunology.

[3]  A. Bairoch,et al.  A unique signature identifies a family of zinc‐dependent metallopeptidases , 1989, FEBS letters.

[4]  A. Amoroso,et al.  Self class I molecules protect normal cells from lysis mediated by autologous natural killer cells , 1994, European journal of immunology.

[5]  M. Moos Isolation of Proteins for Microsequence Analysis , 1992 .

[6]  A. M. Lawson,et al.  Oligosaccharide ligands for NKR-P1 protein activate NK cells and cytotoxicity , 1994, Nature.

[7]  W. Yokoyama Natural killer cell receptors specific for major histocompatibility complex class I molecules. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[8]  P. Parham,et al.  NKB1: a natural killer cell receptor involved in the recognition of polymorphic HLA-B molecules , 1994, The Journal of experimental medicine.

[9]  L. Lanier,et al.  Human NKR-P1A. A disulfide-linked homodimer of the C-type lectin superfamily expressed by a subset of NK and T lymphocytes. , 1994, Journal of immunology.

[10]  F. Bach,et al.  Gamma ray-induced loss of expression of HLA and glyoxalase I alleles in lymphoblastoid cells. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[11]  F. Sánchez‐Madrid,et al.  Molecular cloning, expression, and chromosomal localization of the human earliest lymphocyte activation antigen AIM/CD69, a new member of the C-type animal lectin superfamily of signal-transmitting receptors , 1993, The Journal of experimental medicine.

[12]  P. Parham,et al.  The Bw4 public epitope of HLA-B molecules confers reactivity with natural killer cell clones that express NKB1, a putative HLA receptor , 1995, The Journal of experimental medicine.

[13]  W. Seaman,et al.  Ly-49A, a receptor for H-2Dd, has a functional carbohydrate recognition domain. , 1994, Immunity.

[14]  W. Seaman,et al.  A natural killer cell receptor specific for a major histocompatibility complex class I molecule , 1994, The Journal of experimental medicine.

[15]  E. Ciccone,et al.  P58 molecules as putative receptors for major histocompatibility complex (MHC) class I molecules in human natural killer (NK) cells. Anti-p58 antibodies reconstitute lysis of MHC class I-protected cells in NK clones displaying different specificities , 1993, The Journal of experimental medicine.

[16]  P. Parham,et al.  The NKB1 and HP-3E4 NK cells receptors are structurally distinct glycoproteins and independently recognize polymorphic HLA-B and HLA-C molecules. , 1995, Journal of immunology.

[17]  J. Guardiola,et al.  Evidence of a natural killer (NK) cell repertoire for (allo) antigen recognition: definition of five distinct NK-determined allospecificities in humans , 1992, The Journal of experimental medicine.

[18]  Eric O Long,et al.  Peptide specificity in the recognition of MHC class I by natural killer cell clones , 1995, Science.

[19]  G. Ferrara,et al.  HLA-C is the inhibitory ligand that determines dominant resistance to lysis by NK1- and NK2-specific natural killer cells. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[20]  P. Romeo,et al.  Human CD3−CD16+ natural killer cells express the hGATA‐3 T cell transcription factor and an unrearranged 2.3‐kb TcR δ transcript , 1993, European journal of immunology.

[21]  W. Yokoyama,et al.  MHC class I alloantigen specificity of Ly-49+ IL-2-activated natural killer cells , 1992, Nature.

[22]  E. Ciccone,et al.  Identification of four subsets of human CD3-CD16+ natural killer (NK) cells by the expression of clonally distributed functional surface molecules: correlation between subset assignment of NK clones and ability to mediate specific alloantigen recognition , 1990, The Journal of experimental medicine.

[23]  B. Dupont,et al.  Cell surface phenotype of a cloned line of human natural killer cells. , 1982, Journal of immunology.

[24]  R. A. Phillips,et al.  Natural killer (NK) cells are present in mice with severe combined immunodeficiency (scid). , 1985, Journal of immunology.

[25]  A. F. Williams,et al.  The immunoglobulin superfamily--domains for cell surface recognition. , 1988, Annual review of immunology.

[26]  Dan R. Littman,et al.  Signal transduction by lymphocyte antigen receptors , 1994, Cell.

[27]  V. Stewart,et al.  RAG-2-deficient mice lack mature lymphocytes owing to inability to initiate V(D)J rearrangement , 1992, Cell.

[28]  E. Coligan Current protocols in immunology , 1991 .

[29]  E. Ciccone,et al.  The human natural killer cell receptor for major histocompatibility complex class I molecules. Surface modulation of p58 molecules and their linkage to CD3 ζ chain, FcϵRI γ chain and the p56lck kinase , 1994 .

[30]  A. Amoroso,et al.  Involvement of HLA class I alleles in natural killer (NK) cell-specific functions: expression of HLA-Cw3 confers selective protection from lysis by alloreactive NK clones displaying a defined specificity (specificity 2) , 1992, The Journal of experimental medicine.

[31]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[32]  D. Raulet,et al.  Multiple natural killer cell‐activating signals are inhibited by major histocompatibility complex class I expression in target cells , 1994, European journal of immunology.

[33]  M. López-Botet,et al.  Human natural killer cell receptors for HLA-class I molecules. Evidence that the Kp43 (CD94) molecule functions as receptor for HLA-B alleles , 1994, The Journal of experimental medicine.

[34]  W. Seaman,et al.  The Ly-49 and NKR-P1 gene families encoding lectin-like receptors on natural killer cells: the NK gene complex. , 1993, Annual review of immunology.

[35]  K. Kane,et al.  Ly-49 mediates EL4 lymphoma adhesion to isolated class I major histocompatibility complex molecules , 1994, The Journal of experimental medicine.

[36]  T. Sekiya,et al.  Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. , 1989, Genomics.

[37]  D. Raulet,et al.  Binding of diverse peptides to MHC class I molecules inhibits target cell lysis by activated natural killer cells. , 1995, Immunity.

[38]  Eric O Long,et al.  Recognition of virus-infected cells by natural killer cell clones is controlled by polymorphic target cell elements , 1993, The Journal of experimental medicine.

[39]  H. Ljunggren,et al.  In search of the 'missing self': MHC molecules and NK cell recognition. , 1990, Immunology today.

[40]  L. Moretta,et al.  Coexpression of two functionally independent p58 inhibitory receptors in human natural killer cell clones results in the inability to kill all normal allogeneic target cells. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[41]  G. Pantaleo,et al.  A novel surface antigen expressed by a subset of human CD3- CD16+ natural killer cells. Role in cell activation and regulation of cytolytic function , 1990, The Journal of experimental medicine.

[42]  M. Mitchell,et al.  Organization of human T-cell receptor beta-chain genes: clusters of V beta genes are present on chromosomes 7 and 9. , 1993, Proceedings of the National Academy of Sciences of the United States of America.