Involvement of Endoplasmic Reticulum Stress in Inflammatory Bowel Disease: A Different Implication for Colonic and Ileal Disease?

被引:63
作者
Bogaert, Sara [1 ]
De Vos, Martine [1 ]
Olievier, Kim [1 ]
Peeters, Harald [1 ]
Elewaut, Dirk [2 ]
Lambrecht, Bart [3 ]
Pouliot, Philippe [3 ]
Laukens, Debby [1 ]
机构
[1] Univ Ghent, Dept Gastroenterol, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Rheumatol, B-9000 Ghent, Belgium
[3] Univ Ghent, Lab Immunoregulat & Mucosal Immunol, B-9000 Ghent, Belgium
来源
PLOS ONE | 2011年 / 6卷 / 10期
关键词
UNFOLDED PROTEIN RESPONSE; XBP1; MESSENGER-RNA; ER STRESS; ATF6; EXPRESSION; IRE1; TRANSLATION; INHIBITION; CLEAVAGE; KINASE;
D O I
10.1371/journal.pone.0025589
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
Background: Endoplasmic reticulum (ER) stress has been suggested to play a role in inflammatory bowel disease (IBD). The three branches (ATF6, IRE1 and PERK) of the unfolded protein response (UPR) have different roles and are not necessarily activated simultaneously. Methodology/Principal Findings: Expression of UPR-related genes was investigated in colonic and ileal biopsies of 23 controls, 15 ulcerative colitis (UC) and 54 Crohn's disease (CD) patients. This expression was confirmed at protein level in colonic and ileal samples of five controls, UC and CD patients. HSPA5, PDIA4 and XBP1s were significantly increased in colonic IBD at mRNA and/or protein levels, indicating activation of the ATF6 and IRE1 branch. Colonic IBD was associated with increased phosphorylation of EIF2A suggesting the activation of the PERK branch, but subsequent induction of GADD34 was not observed. In ileal CD, no differential expression of the UPR-related genes was observed, but our data suggested a higher basal activation of the UPR in the ileal mucosa of controls. This was confirmed by the increased expression of 16 UPR-related genes as 12 of them were significantly more expressed in ileal controls compared to colonic controls. Tunicamycin stimulation of colonic and ileal samples of healthy individuals revealed that although the ileal mucosa is exhibiting this higher basal UPR activation, it is still responsive to ER stress, even more than colonic mucosa. Conclusions/Significance: Activation of the three UPR-related arms is seen in colonic IBD-associated inflammation. However, despite EIF2A activation, inflamed colonic tissue did not increase GADD34 expression, which is usually involved in re-establishment of ER homeostasis. This study also implies the presence of a constitutive UPR activation in healthy ileal mucosa, with no further activation during inflammation. Therefore, engagement of the UPR differs between colon and ileum and this could be a factor in the development of ileal or colonic disease.
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页数:12
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共 43 条
[1]   A genome scan in 260 inflammatory bowel disease-affected relative pairs [J].
Barmada, MM ;
Brant, SR ;
Nicolae, DL ;
Achkar, JP ;
Panhuysen, CI ;
Bayless, TM ;
Cho, JH ;
Duerr, RH .
INFLAMMATORY BOWEL DISEASES, 2004, 10 (01) :15-22
[2]   Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response [J].
Bertolotti, A ;
Zhang, YH ;
Hendershot, LM ;
Harding, HP ;
Ron, D .
NATURE CELL BIOLOGY, 2000, 2 (06) :326-332
[3]   Increased sensitivity to dextran sodium sulfate colitis in IRE1β-deficient mice [J].
Bertolotti, A ;
Wang, XZ ;
Novoa, I ;
Jungreis, R ;
Schlessinger, K ;
Cho, JH ;
West, AB ;
Ron, D .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (05) :585-593
[4]   Acute Tissue Injury Caused by Subcutaneous Fat Biopsies Produces Endoplasmic Reticulum Stress [J].
Boden, Guenther ;
Silviera, Matthew ;
Smith, Brian ;
Cheung, Peter ;
Homko, Carol .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 95 (01) :349-352
[5]   The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments [J].
Bustin, Stephen A. ;
Benes, Vladimir ;
Garson, Jeremy A. ;
Hellemans, Jan ;
Huggett, Jim ;
Kubista, Mikael ;
Mueller, Reinhold ;
Nolan, Tania ;
Pfaffl, Michael W. ;
Shipley, Gregory L. ;
Vandesompele, Jo ;
Wittwer, Carl T. .
CLINICAL CHEMISTRY, 2009, 55 (04) :611-622
[6]   IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA [J].
Calfon, M ;
Zeng, HQ ;
Urano, F ;
Till, JH ;
Hubbard, SR ;
Harding, HP ;
Clark, SG ;
Ron, D .
NATURE, 2002, 415 (6867) :92-96
[7]   Increased interleukin 8 expression in the colon mucosa of patients with inflammatory bowel disease [J].
Daig, R ;
Andus, T ;
Aschenbrenner, E ;
Falk, W ;
Scholmerich, J ;
Gross, V .
GUT, 1996, 38 (02) :216-222
[8]   A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort [J].
Hampe, J ;
Schreiber, S ;
Shaw, SH ;
Lau, KF ;
Bridger, S ;
Macpherson, AJS ;
Cardon, LR ;
Sakul, H ;
Harris, TJR ;
Buckler, A ;
Hall, J ;
Stokkers, P ;
van Deventer, SJH ;
Nürnberg, P ;
Mirza, MM ;
Lee, JCW ;
Lennard-Jones, JE ;
Mathew, CG ;
Curran, ME .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (03) :808-816
[9]   Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase [J].
Harding, HP ;
Zhang, YH ;
Ron, D .
NATURE, 1999, 397 (6716) :271-274
[10]   Regulated translation initiation controls stress-induced gene expression in mammalian cells [J].
Harding, HP ;
Novoa, I ;
Zhang, YH ;
Zeng, HQ ;
Wek, R ;
Schapira, M ;
Ron, D .
MOLECULAR CELL, 2000, 6 (05) :1099-1108