Peroxisome proliferator-activated receptor-γ and thymic stromal lymphopoietin are involved in the pathophysiology of childhood coeliac disease

• Published in: Virchows Archiv : an international journal of pathology Vol. 465; no. 4; pp. 385 - 393
• Main Authors: Sziksz, Erna, Molnár, Kriszta, Lippai, Rita, Pap, Domonkos, Ónody, Anna, Veres-Székely, Apor, Vörös, Péter, Szabó, Dolóresz, Győrffy, Hajnalka, Veres, Gábor, Tulassay, Tivadar, Vannay, Ádám, Arató, András
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01-10-2014
• Subjects: Adolescent; Blotting, Western; Celiac Disease - diet therapy; Celiac Disease - metabolism; Child; Child, Preschool; Cytokines - metabolism; Diet, Gluten-Free; Duodenum - pathology; Female; Humans; Immunohistochemistry; Intestinal Mucosa - pathology; Male; Medicine; Medicine & Public Health; Original Article; Pathology; PPAR gamma - metabolism; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Duodenal biopsies; Children; TSLP; Coeliac disease; PPARγ
• ISSN: 0945-6317; 1432-2307
• DOI: 10.1007/s00428-014-1650-2

Celiac disease (CD) is a chronic autoimmune enteropathy caused by exposure to dietary gluten in genetically predisposed individuals. The transcription factor peroxisome proliferator-activated receptor gamma (PPARγ) was shown to exert protective effects in several immune-mediated disorders. Activation of PPARγ suppressed the expression of thymic stromal lymphopoietin (TSLP), an inducer of proinflammatory cytokines. Since the role of TSLP in gluten-sensitive enteropathy is completely unknown, we investigated the involvement of TSLP and its regulator PPARγ in childhood CD. We collected duodenal biopsy specimens from 19 children with newly diagnosed CD, 6 children with treated CD (gluten-free diet, GFD), and 10 controls. Expression of mRNA and protein levels of PPARγ, TSLP, and TSLP receptor were determined by real-time RT-PCR and Western blot, respectively. Duodenal localization of PPARγ and TSLP was studied by immunohistochemistry. In duodenal mucosa of children with CD, the amount of PPARγ was significantly lower and simultaneously that of TSLP significantly higher compared to controls (
p
 < 0.05). In GFD-treated patients, the levels of PPARγ mRNA and protein were significantly higher while that of TSLP markedly lower compared to newly diagnosed CD (
p
 < 0.05). Immunohistochemistry revealed PPARγ and TSLP expression in lamina propria immune cells and in enterocytes. Low expression of PPARγ and high expression of TSLP in the duodenal mucosa of children with newly diagnosed CD suggest that they are involved in the pathophysiology of CD. We hypothesize that PPARγ may be an inhibitory regulator of TSLP-stimulated inflammatory processes in CD.