Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease

被引:30
|
作者
Allegretti, Yessica L. [1 ]
Bondar, Constanza [1 ]
Guzman, Luciana [2 ]
Cueto Rua, Eduardo [2 ]
Chopita, Nestor [3 ]
Fuertes, Mercedes [4 ,5 ]
Zwirner, Norberto W. [4 ,6 ]
Chirdo, Fernando G. [1 ]
机构
[1] Univ Nacl La Plata, Fac Ciencias Exactas, Dept Ciencias Biol, Lab Invest Sistema Inmune LISIN, La Plata, Buenos Aires, Argentina
[2] Hosp Ninos Sor Maria Ludovica, Serv Gastroenterol, La Plata, Buenos Aires, Argentina
[3] Hosp San Martin La Plata, Serv Gastroenterol, La Plata, Buenos Aires, Argentina
[4] Consejo Nacl Invest Cient & Tecn CONICET, Lab Fisiopatol Inmunidad Innata, IBYME, Buenos Aires, DF, Argentina
[5] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Biol, Buenos Aires, DF, Argentina
[6] Univ Buenos Aires, Fac Med, Dept Microbiol Parasitol & Inmunol, Buenos Aires, DF, Argentina
来源
PLOS ONE | 2013年 / 8卷 / 09期
关键词
MHC-CLASS-I; ACTIVATED T-LYMPHOCYTES; SMALL-INTESTINAL MUCOSA; OXIDATIVE STRESS; EPITHELIAL-CELLS; IMMUNE-RESPONSE; CHAIN-A; NKG2D; GLIADIN; LIGANDS;
D O I
10.1371/journal.pone.0073658
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The MICA/B genes (MHC class I chain related genes A and B) encode for non conventional class I HLA molecules which have no role in antigen presentation. MICA/B are up-regulated by different stress conditions such as heat-shock, oxidative stress, neoplasic transformation and viral infection. Particularly, MICA/B are expressed in enterocytes where they can mediate enterocyte apoptosis when recognised by the activating NKG2D receptor present on intraepithelial lymphocytes. This mechanism was suggested to play a major pathogenic role in active celiac disease (CD). Due to the importance of MICA/B in CD pathogenesis we studied their expression in duodenal tissue from CD patients. By immunofluorescence confocal microscopy and flow cytometry we established that MICA/B was mainly intracellularly located in enterocytes. In addition, we identified MICA/B+ T cells in both the intraepithelial and lamina propria compartments. We also found MICA/B+ B cells, plasma cells and some macrophages in the lamina propria. The pattern of MICA/B staining in mucosal tissue in severe enteropathy was similar to that found in in vitro models of cellular stress. In such models, MICA/B were located in stress granules that are associated to the oxidative and ER stress response observed in active CD enteropathy. Our results suggest that expression of MICA/B in the intestinal
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页数:12
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