Expression of functional CD32 molecules on human NK cells is determined by an allelic polymorphism of the FcγRIIC gene

被引:96
作者
Metes, D
Ernst, LK
Chambers, WH
Sulica, A
Herberman, RB
Morel, PA
机构
[1] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Sch Med, Dept Med, Pittsburgh, PA 15261 USA
[5] Inst Virol, Ctr Immunol, Bucharest, Romania
关键词
D O I
10.1182/blood.V91.7.2369.2369_2369_2380
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human natural killer (NK) cells were thought to express only Fc gamma RIIIA (CD16), but recent reports have indicated that NK cells also express a second type of Fc gamma R, ie, Fc gamma RII (CD32). We have isolated, cloned, and sequenced full-length cDNAs of Fc gamma RII from NK cells derived from several normal individuals that may represent four different products of the Fc gamma RIIC gene. One transcript (IIc1) is identical with the already described Fc gamma RIIc form. The other three (IIc2-IIc4) appear to represent unique, alternatively spliced products of the same gene, and include a possible soluble form. Analyses of the full-length clones have revealed an allelic polymorphism in the first extracellular exon, resulting in either a functional open reading frame isoform or a null allele. Stable transfection experiments enabled us to determine a unique binding pattern of anti-CD32 monoclonal antibodies to Fc gamma RIIc. Further analyses of NK-cell preparations revealed heterogeneity in CD32 expression, ranging from donors racking CD32 expression to donors expressing high levels of CD32 that were capable of triggering cytotoxicity. Differences in expression were correlated with the presence or absence of null alleles. These data show that certain individuals express high levels of functional Fc gamma RIIc isoforms on their NK cells. (C) 1998 by The American Society of Hematology.
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页码:2369 / 2380
页数:12
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