Tu1845 Mesenteric Preadipocytes From Crohn's Disease Patients Exhibit Differential mRNA Expression Patterns and Induce Protective Responses in Colonic Epithelial Cells and Mice With Colitis

2016 ◽  
Vol 150 (4) ◽  
pp. S959
Author(s):  
Jill M. Hoffman ◽  
Aristea Sideri ◽  
Jonathan J. Ruiz ◽  
Dimitris Stavrakis ◽  
Charalabos Pothoulakis ◽  
...  
PLoS ONE ◽  
2019 ◽  
Vol 14 (2) ◽  
pp. e0212850 ◽  
Author(s):  
Stephen M. Matthews ◽  
Melanie A. Eshelman ◽  
Arthur S. Berg ◽  
Walter A. Koltun ◽  
Gregory S. Yochum

2005 ◽  
Vol 43 (05) ◽  
Author(s):  
J Büning ◽  
G Hundorfean ◽  
M Schmitz ◽  
KP Zimmer ◽  
S Strobel ◽  
...  

2020 ◽  
Vol 38 (5) ◽  
pp. 398-407
Author(s):  
Stefan Reischl ◽  
Jasmin Troger ◽  
Moritz Jesinghaus ◽  
Atsuko Kasajima ◽  
Dirk Felix Wilhelm ◽  
...  

Introduction: Crohn’s disease (CD) is characterized by relapsing intestinal inflammation. The anti-inflammatory protein annexin A1 (ANXA1) has been linked to inflammatory processes in the gut. Objective: To examine ANXA1 expression patterns in the inflamed intestine of patients with CD and associate ANXA1 expression capacity with disease characteristics. Methods: Surgical specimens of patients with CD operated between 2003 and 2015 were examined. Immunohistochemistry and immunofluorescence were performed to delineate ANXA1 expression. Those with pronounced ANXA1 expression were included in further analysis by qPCR. ANXA1 mRNA expression ratio of the inflamed to non-inflamed tissue was determined and defined as expression capacity of the tissue. Depending on their expression capacity, patients were divided into 2 groups (ANXA1-low vs. ANXA1-high), which were associated with clinical characteristics. Results: Immunohistochemical ANXA1 expression was localized in inflamed regions of the intestine. In immunofluorescence, ANXA1 costained with myeloperoxidase as neutrophil marker, CD4 and CD8 as T cell marker but not CD20 as B cell marker or CD68 as macrophage marker. In qPCR, ANXA1 mRNA expression was upregulated by 20-fold in inflamed to noninflamed tissues. Patients with higher intrinsic ANXA1 expression capacity had significantly less severity of inflammation. Furthermore, the ANXA1-high group had significantly more locally restricted disease (p = 0.0070), more stricturating disease (p = 0.0037), and was less frequently treated by preoperative steroid therapy (p = 0.030). Conclusions: ANXA1 expression was strongly associated with intestinal inflammation and expressed in T cells and neutrophils of the CD tissues. Patients with higher intrinsic ANXA1 expression capacity of the inflamed tissue presented milder inflammatory changes and indolent clinical course.


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