TAP1 MUTANT MICE ARE DEFICIENT IN ANTIGEN PRESENTATION, SURFACE CLASS-I MOLECULES, AND CD4-8+ T-CELLS

被引:0
作者
VANKAER, L
ASHTONRICKARDT, PG
PLOEGH, HL
TONEGAWA, S
机构
[1] MIT, CTR CANC RES, CAMBRIDGE, MA 02139 USA
[2] MIT, DEPT BIOL, CAMBRIDGE, MA 02139 USA
关键词
D O I
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中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transporter associated with the antigen processing 1 (TAP1) gene encodes a subunit for a transporter, presumed to be involved in the delivery of peptides across the endoplasmic reticulum membrane to class I molecules. We have generated mice with a disrupted TAP1 gene using embryonic stem cell technology. TAP1-deficient mice are defective in the stable assembly and intracellular transport of class I molecules and consequently show severely reduced levels of surface class I molecules. These properties are strikingly similar to those described for the TAP2 mutant cell line RMA-S. Cells from the TAP1-deficient mice are unable to present cytosolic antigens to class I-restricted cytotoxic T cells. As predicted from the near absence of class I surface expression, TAP1-deficient mice lack CD4-8+ T cells.
引用
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页码:1205 / 1214
页数:10
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