HLA-B27 polymorphism at position 116 critically influences the association with TAP/tapasin, intracellular trafficking and conformational homodimers formation

被引:17
作者
Blanco-Gelaz, M. A. [1 ]
Suarez-Alvareza, B. [1 ]
Diaz-Pena, R. [1 ]
Lopez-Larrea, C. [1 ,2 ]
机构
[1] Hosp Univ Cent Asturias, Histocompatibil & Transplantat Unit, Oviedo 33006, Spain
[2] Fdn Renal Inigo Alvarez de Toledo, Madrid, Spain
关键词
Spondyloarthropathies; Immunopathogenesis; Antigen processing; Homodimer; ANKYLOSING-SPONDYLITIS; SURFACE EXPRESSION; CELL-LINE; HLA-B; ENDOPLASMIC-RETICULUM; MONOCLONAL-ANTIBODY; PEPTIDE; ANTIGEN; TAPASIN; SUSCEPTIBILITY;
D O I
10.1016/j.molimm.2008.11.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
HLA-B27 confers susceptibility to ankylosing spondylitis but AS disease mechanisms remain unknown. We determined here the effect of polymorphism and tapasin dependence on the expression, intracellular maturation and homodimer formation among HLA-B27 subtypes. We found that B*2709 with a histidine at position 116 was strongly associated with the transporter associated with antigen processing complex, correlated with lower, non-conformational expression on the cell surface, delayed maturation rate and minimal conformational and non-conformational homodimer formation. in contrast, B*2705 showed a low dependence for transporter associated with antigen processing, faster intracellular maturation and increased levels of homodimeric forms. The absence of tapasin significantly influenced the rate of intracellular maturation of B*2709, showing faster transport out of the endoplasmic reticulum, but similar to that of B*2705. All B27 subtypes examined were unable to express conformational homodimeric forms in the absence of tapasin. This study suggests that HLA-B27 polymorphism drives the tapasin dependency, rates of intracellular maturation and expressions of homodimers. (C) 2009 Published by Elsevier Ltd.
引用
收藏
页码:1304 / 1311
页数:8
相关论文
共 36 条
[1]
Allen RL, 1999, J IMMUNOL, V162, P5045
[2]
Formation of HLA-B27 homodimers and their relationship to assembly kinetics [J].
Antoniou, AN ;
Ford, S ;
Taurog, JD ;
Butcher, GW ;
Powis, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (10) :8895-8902
[3]
Susceptibility to ankylosing spondylitis is independent of the Bw4 and Bw6 epitopes of HLA-B27 alleles [J].
Armas, JB ;
Gonzalez, S ;
Martinez-Borra, J ;
Laranjeira, F ;
Ribeiro, E ;
Correia, J ;
Ferreira, ML ;
Toste, M ;
López-Vazquez, A ;
López-Larrea, C .
TISSUE ANTIGENS, 1999, 53 (03) :237-243
[4]
Lymphoblastoid cells express HLA-1327 homodimers both intracellularly and at the cell surface following endosomal recycling [J].
Bird, LA ;
Peh, CA ;
Kolinberger, S ;
Elliott, T ;
McMichael, AJ ;
Bowness, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (03) :748-759
[5]
The amino acid at position 97 is involved in folding and surface expression of HLA-B27 [J].
Blanco-Gelaz, MA ;
Suárez-Alvarez, B ;
González, S ;
López-Vázquez, A ;
Martínez-Borra, J ;
López-Larrea, C .
INTERNATIONAL IMMUNOLOGY, 2006, 18 (01) :211-220
[6]
BREWERTON DA, 1973, LANCET, V1, P904
[7]
HLA-B27 misfolding: a solution to the spondyloarthropathy conundrum? [J].
Colbert, RA .
MOLECULAR MEDICINE TODAY, 2000, 6 (06) :224-230
[8]
RELEVANCE OF RESIDUE-116 OF HLA-B27 IN DETERMINING SUSCEPTIBILITY TO ANKYLOSING-SPONDYLITIS [J].
DAMATO, M ;
FIORILLO, MT ;
CARCASSI, C ;
MATHIEU, A ;
ZUCCARELLI, A ;
BITTI, PP ;
TOSI, R ;
SORRENTINO, R .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (11) :3199-3201
[9]
HLA-B27 misfolding is associated with aberrant intermolecular disulfide bond formation (dimerization) in the endoplasmic reticulum [J].
Dangoria, NS ;
DeLay, ML ;
Kingsbury, DJ ;
Mear, JP ;
Uchanska-Ziegler, B ;
Ziegler, A ;
Colbert, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (26) :23459-23468
[10]
HLA-B27:: a registry of constitutive peptide ligands [J].
de Castro, JAL ;
Alvarez, I ;
Marcilla, M ;
Paradela, A ;
Ramos, M ;
Sesma, L ;
Vázquez, M .
TISSUE ANTIGENS, 2004, 63 (05) :424-445