The molecular basis of Natural Killer (NK) cell recognition and function

被引:39
作者
Moretta, L
Mingari, MC
Pende, D
Bottino, C
Biassoni, R
Moretta, A
机构
[1] UNIV GENOA,IST PATOL GEN,GENOA,ITALY
[2] UNIV GENOA,DIPARTIMENTO MED & ONCOL SPERIMENTALE,GENOA,ITALY
[3] UNIV GENOA,DIPARTIMENTO SCI BIOMED & BIOTECNOL,GENOA,ITALY
关键词
natural killer (NK) cells; NK cell recognition; NK cell function; NK cell receptors;
D O I
10.1007/BF01541388
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural Killer cells are likely to play an important role in the host defenses because they kill virally infected or tumor cells but spare normal self-cells. The molecular mechanism that explains why NK cells do not kill indiscriminately has recently been elucidated. It is due to several specialized receptors that recognize major histocompatibility complex (MHC) class I molecules expressed on normal cells. The lack of expression of one or more HLA class I alleles leads to NK-mediated target cell lysis. Different types of receptors specific for groups of HLA-C, HLA-B, and, very recently, HLA-A alleles have been identified. While in most instances, they function as inhibitory receptors, an activatory form of the HLA-C-specific receptors has been identified in some donors. Molecular cloning of HLA-C-, HLA-B- or HLA-A-specific receptors has revealed new members of the immunoglobulin superfamily with two or three Ig-like domains, respectively, in their extracellular portion. While the inhibitory form is characterized by a long cytoplasmic tail associated with a non-polar transmembrane portion, the activatory one has a short tail asociated with a Lys-containing transmembrane portion. Thus, these human Mt receptors are different from the murine Ly49, that is a type II transmembrane protein characterized by a C-type lectin domain. A subset of activated T lymphocytes expresses NK-type class I-specific receptors. These receptors exert an inhibiting activity on T cell receptor-mediated functions and may provide an important mechanism of downregulation of T cell responses.
引用
收藏
页码:243 / 253
页数:11
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