Cutting edge: Murine UL16-binding protein-like transcript 1: A newly described transcript encoding a high-affinity ligand for marine NKG2D

被引:222
作者
Carayannopoulos, LN
Naidenko, OV
Fremont, DH
Yokoyama, WM
机构
[1] Washington Univ, Sch Med, Div Rheumatol, St Louis, MO 63110 USA
[2] Barnes Jewish Hosp, Div Pulm & Crit Care Med, St Louis, MO 63110 USA
[3] Barnes Jewish Hosp, Dept Pathol & Immunol, St Louis, MO 63110 USA
[4] Barnes Jewish Hosp, Div Rheumatol, St Louis, MO 63110 USA
[5] Barnes Jewish Hosp, Howard Hughes Med Inst, St Louis, MO 63110 USA
关键词
D O I
10.4049/jimmunol.169.8.4079
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Murine NKG2D is known to recognize H60 and five RAE1 variants. The human homologue recognizes both inducible MHC class I chain-related gene and constitutive (UL16-binding protein (ULBP)) ligands. Widely expressed, the latter are thought to mark transformed or infected cells for destruction by NK cells in the context of down-regulated cell surface class I (i.e., the "missing self"-response). Unlike MIC and ULBP however, mRNA for the murine ligands appears only in very limited contexts in the mature animal. In this study, we describe a NKG2D ligand termed "murine ULBP-like transcript 1 (MULT1) whose mRNA appears to be widely expressed in adult parenchyma. This molecule possesses MHC class I-like alpha1 and alpha2 domains as well as a large cytoplasmic domain. Recombinant MULT1 binds NKG2D with relatively high affinity (K-D approximate to 6 nM) and low k(off) (similar to 0.006s(-1)). Expression of MULT1 by normally resistant RMA cells results in their susceptibility to lysis by C57BL/6 splenocytes.
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页码:4079 / 4083
页数:5
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