The multiple roles of major histocompatibility complex class-I-like molecules in mucosal immune function

被引:12
作者
Blumberg, RS
van de Wal, Y
Claypool, S
Corazza, N
Dickinson, B
Nieuwenhuis, E
Pitman, R
Spiekermann, G
Zhu, XP
Colgan, S
Lencer, WI
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Gastroenterol, Boston, MA 02115 USA
[2] Harvard Univ, Childrens Hosp, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
epithelium; intestine; major histocompatibility complex;
D O I
10.1080/000163501750266729
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The human major histocompatibility complex (MHC) on chromosome 6 encodes three classical class-I genes: human leukocyte antigens (HLA) A, B, and C. These polymorphic genes encode a 43- to 45-kDa cell surface glycoprotein that, in association with the 12-kDa beta (2)-microglobulin molecule, functions in the presentation of nine amino acid peptides to the T-cell receptor of CD8-bearing T lymphocytes and killer inhibitory receptors on natural killer cells. In addition to these ubiquitously expressed, polymorphic proteins, the human genome also encodes several nonclassical MHC class-I-like, or class Ib, genes that, in general, encode nonpolymorphic molecules involved in various specific immunological functions. Many of these genes, including CD1, the neonatal Fe receptor for IgG, HLA-G, HLA-E, the MHC class-I chain-related gene A, and Hfe, are prominently displayed on epithelial cells, suggesting an important role in epithelial cell biology.
引用
收藏
页码:139 / 144
页数:6
相关论文
共 47 条
[41]  
SANCHEZ LM, 1997, P NATL ACAD SCI USA, V94, P46216
[42]   Activation of natural killer T cells by α-galactosylceramide in the presence of CD1d provides protection against colitis in mice [J].
Saubermann, LJ ;
Beck, P ;
De Jong, YP ;
Pitman, RS ;
Ryan, MS ;
Kim, HS ;
Exley, M ;
Snapper, S ;
Balk, SP ;
Hagen, SJ ;
Kanauchi, O ;
Motoki, K ;
Sakai, T ;
Terhorst, C ;
Koezuka, Y ;
Podolsky, DK ;
Blumberg, RS .
GASTROENTEROLOGY, 2000, 119 (01) :119-+
[43]   Immunolocalization of CD1d in human intestinal epithelial cells and identification of a β2-microglobulin-associated form [J].
Somnay-Wadgaonkar, K ;
Nusrat, A ;
Kim, HS ;
Canchis, WP ;
Balk, SP ;
Colgan, SP ;
Blumberg, RS .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (03) :383-392
[44]   Cytoplasmic tail-dependent localization of CD1b antigen-presenting molecules to MIICs [J].
Sugita, M ;
Jackman, RM ;
vanDonselaar, E ;
Behar, SM ;
Rogers, RA ;
Peters, PJ ;
Brenner, MB ;
Porcelli, SA .
SCIENCE, 1996, 273 (5273) :349-352
[45]   MOLECULAR COMPARISONS OF THE BETA-2-MICROGLOBULIN-BINDING SITE IN CLASS-I MAJOR-HISTOCOMPATIBILITY-COMPLEX ALPHA-CHAINS AND PROTEINS OF RELATED SEQUENCES [J].
TYSOECALNON, VA ;
GRUNDY, JE ;
PERKINS, SJ .
BIOCHEMICAL JOURNAL, 1991, 277 :359-369
[46]  
VANDERVEN K, 1994, J IMMUNOL, V153, P5628
[47]   Crystal structure of mouse CD1: An MHC-like fold with a large hydrophobic binding groove [J].
Zeng, ZH ;
Castano, AR ;
Segelke, BW ;
Stura, EA ;
Peterson, PA ;
Wilson, IA .
SCIENCE, 1997, 277 (5324) :339-345