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Published in: BMC Gastroenterology 1/2011

Open Access 01-12-2011 | Research article

Distribution of enteric glia and GDNF during gut inflammation

Authors: Georg BT von Boyen, Nadine Schulte, Carolin Pflüger, Ulrike Spaniol, Christoph Hartmann, Martin Steinkamp

Published in: BMC Gastroenterology | Issue 1/2011

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Abstract

Background

The enteric glia network may be involved in the pathogenesis of inflammatory bowel disease (IBD). Enteric glia cells (EGCs) are the major source of glial-derived neurotrophic factor (GDNF), which regulates apoptosis of enterocytes. The aim of the study was to determine the distribution of EGCs and GDNF during gut inflammation and to elucidate a possible diminished enteric glia network in IBD.

Methods

The expression of glial fibrillary acidic protein (GFAP) in colonic biopsies of patients with IBD, controls and patients with infectious colitis was detected by immunohistochemistry and Western blot. Tissue GDNF levels were measured by ELISA.

Results

The expression of GFAP and GDNF in the mucosal plexus is highly increased in the inflamed colon of patients with ulcerative colitis (UC) and infectious colitis. Although the GDNF and GFAP content are increased in Crohn's disease (CD), it is significantly less. Additionally the non-inflamed colon of CD patients showed a reduced GFAP and no GDNF expression compared to controls and the non-inflamed colon of UC patients.

Conclusions

GFAP and GDNF as signs of activated EGCs are increased in the inflamed mucosa of patients with UC and infectious colitis, which underline an unspecific role of EGC in the regulation of intestinal inflammation. The reduced GFAP and GDNF content in the colon of CD patients suggest a diminished EGC network in this disease. This might be a part of the pathophysiological puzzle of CD.
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Metadata
Title
Distribution of enteric glia and GDNF during gut inflammation
Authors
Georg BT von Boyen
Nadine Schulte
Carolin Pflüger
Ulrike Spaniol
Christoph Hartmann
Martin Steinkamp
Publication date
01-12-2011
Publisher
BioMed Central
Published in
BMC Gastroenterology / Issue 1/2011
Electronic ISSN: 1471-230X
DOI
https://doi.org/10.1186/1471-230X-11-3

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