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Erschienen in: Journal of Clinical Immunology 4/2009

01.07.2009

Enhanced Expression of Transcription Factor GATA-4 in Inflammatory Bowel Disease and Its Possible Regulation by TGF-β1

verfasst von: Hanna Haveri, Merja Ashorn, Sari Iltanen, David B. Wilson, Leif C. Andersson, Markku Heikinheimo

Erschienen in: Journal of Clinical Immunology | Ausgabe 4/2009

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Abstract

Background

Transforming growth factor beta 1 (TGF-β1) promotes epithelial healing in inflammatory bowel disease. We hypothesized that GATA-4, a transcription factor cooperating with TGF-β signaling pathway, is upregulated by TGF-β1 in the inflamed intestinal epithelium.

Methods

Normal and inflamed intestinal samples were subjected to immunohistochemistry for GATA-4/6 and the TGF-β signaling pathway components Smad2/3/4. Proliferation and apoptosis were analyzed using Ki-67 and in situ DNA 3′-end labeling assays and Bax and Bcl-2 immunohistochemistry. Furthermore, GATA-4 was assessed in intestinal Caco-2 cells stimulated with TGF-β1, or interleukin-6 and tumor necrosis factor alpha.

Results

GATA-4 was detected in only 20% of normal intestinal samples, but was upregulated in corresponding inflamed regions. GATA-6 expression remained unchanged during inflammation. TGF-β1 and Smad3/4, but not Smad2, were expressed concomitantly with GATA-4 in inflamed bowel mucosa. In intestinal Caco-2 cells, TGF-β1 upregulated GATA-4 and Smad2/3/4, whereas treatment with control cytokines had no effect. Inflammation was associated with increased epithelial cell apoptosis and the enhancement of Bcl-2, but not Bax.

Conclusions

We surmise GATA-4 expression is upregulated in inflamed intestine correlating with the activation of TGF-β signaling pathway. We speculate that TGF-β1 drives GATA-4 expression during intestinal inflammation, these two components cooperating to promote epithelial healing.
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Metadaten
Titel
Enhanced Expression of Transcription Factor GATA-4 in Inflammatory Bowel Disease and Its Possible Regulation by TGF-β1
verfasst von
Hanna Haveri
Merja Ashorn
Sari Iltanen
David B. Wilson
Leif C. Andersson
Markku Heikinheimo
Publikationsdatum
01.07.2009
Verlag
Springer US
Erschienen in
Journal of Clinical Immunology / Ausgabe 4/2009
Print ISSN: 0271-9142
Elektronische ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-009-9292-x

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