Characterization of guinea-pig group 1 CD1 proteins

被引:52
作者
Hiromatsu, K
Dascher, CC
Sugita, M
Gingrich-Baker, C
Behar, SM
LeClair, KP
Brenner, MB
Porcelli, SA
机构
[1] Brigham & Womens Hosp, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Antigen Inc, Framingham, MA USA
关键词
D O I
10.1046/j.1365-2567.2002.01422.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD1 molecules are cell-surface glycoproteins with strong structural similarities to major histocompatibility complex (MHC) class I molecules, and studies in humans and mice have demonstrated that CD1 proteins perform the unique role of presenting lipid antigens to T lymphocytes. Our previous studies have shown that guinea-pigs, unlike the muroid rodents, have an extended family of group 1 CD1 genes. In the current study, we raised monoclonal anibodies (mAbs) against guinea-pig CD1 proteins and generated transfected cell lines expressing individual members of the guinea-pig CD1 family. Our results indicated that multiple members of the guinea-pig CD1 family, including members that are homologous to the human CD1b and CD1c proteins, are expressed at the protein level in transfected cells and in specialized antigen-presenting cells such as monocyte-derived dendritic cells. In addition, CD1 proteins, especially guinea-pig CD1b3, were expressed on a large number of B cells in the guinea-pig, and CD1 expression appeared to be regulated by B-cell maturation or differentiation. Interestingly, three different patterns of intracellular localization were observed for the various guinea-pig CD1 isoforms, a finding that is reminiscent of the distinct patterns of intracellular localization that have been previously demonstrated for human CD1a, CD1b and CD1c. Taken together, these results provide further evidence for substantial similarities between the guinea-pig and human CD1 systems, thus supporting the possibility that the guinea-pig may offer significant advantages as an animal model for the study of the in vivo role of CD1 proteins in infectious and autoimmune diseases.
引用
收藏
页码:159 / 172
页数:14
相关论文
共 46 条
[21]   NKT cells: facts, functions and fallacies [J].
Godfrey, DI ;
Hammond, KJL ;
Poulton, LD ;
Smyth, MJ ;
Baxter, AG .
IMMUNOLOGY TODAY, 2000, 21 (11) :573-583
[22]   Group 1 CD1 genes in rabbit [J].
Hayes, SM ;
Knight, KL .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :403-410
[23]   COMPARISON OF CD1 MONOCLONAL-ANTIBODIES ON BOVINE CELLS AND TISSUES [J].
HOWARD, CJ ;
SOPP, P ;
BEMBRIDGE, G ;
YOUNG, J ;
PARSONS, KR .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1993, 39 (1-3) :77-83
[24]   GENERATION OF LARGE NUMBERS OF DENDRITIC CELLS FROM MOUSE BONE-MARROW CULTURES SUPPLEMENTED WITH GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR [J].
INABA, K ;
INABA, M ;
ROMANI, N ;
AYA, H ;
DEGUCHI, M ;
IKEHARA, S ;
MURAMATSU, S ;
STEINMAN, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) :1693-1702
[25]   CHARACTERIZATION OF A BOVINE THYMIC DIFFERENTIATION ANTIGEN ANALOGOUS TO CD1 IN THE HUMAN [J].
MACHUGH, ND ;
BENSAID, A ;
DAVIS, WC ;
HOWARD, CJ ;
PARSONS, KR ;
JONES, B ;
KAUSHAL, A .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1988, 27 (05) :541-547
[26]  
MACKAY CR, 1985, IMMUNOLOGY, V55, P729
[27]   CD1c-mediated T-cell recognition of isoprenoid glycolipids in Mycobacterium tuberculosis infection [J].
Moody, DB ;
Ulrichs, T ;
Mühlecker, W ;
Young, DC ;
Gurcha, SS ;
Grant, E ;
Rosat, JP ;
Brenner, MB ;
Costello, CE ;
Besra, GS ;
Porcelli, SA .
NATURE, 2000, 404 (6780) :884-888
[28]  
PORCELLI SA, 1995, ADV IMMUNOL, V59, P1, DOI 10.1016/S0065-2776(08)60629-X
[29]   The CD1 family of lipid antigen-presenting molecules [J].
Porcelli, SA ;
Segelke, BW ;
Sugita, M ;
Wilson, IA ;
Brenner, MB .
IMMUNOLOGY TODAY, 1998, 19 (08) :362-368
[30]   The CD1 system: Antigen-presenting molecules for T cell recognition of lipids and glycolipids [J].
Porcelli, SA ;
Modlin, RL .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :297-329