Journal
JOURNAL OF CLINICAL GASTROENTEROLOGY
Volume 53, Issue 6, Pages 449-456Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MCG.0000000000001011
Keywords
intestinal inflammation; diverticular disease; enteric glial cells; S100 beta
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Funding
- German Research Society (Deutsche Forschungsgemeinschaft, DFG) [WE 2366/4-3]
- Faculty of Medicine, University of Kiel [F356920]
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Background: Diverticular disease (DD) is a common gastrointestinal inflammatory disorder associated with an enteric neuropathy. Although enteric glial cells (EGCs) are essential regulators of intestinal inflammation and motility functions, their contribution to the pathophysiology of DD remains unclear. Therefore, we analyzed the expression of specific EGC markers in patients with DD. Materials and Methods: Expression of the glial markers S100 beta, GFAP, Sox10, and Connexin 43 was analyzed by real-time quantitative PCR in colonic specimens of patients with DD and in that of controls. Protein expression levels of S100 beta, GFAP, and Connexin 43 were further analyzed using immunohistochemistry in the submucosal and myenteric plexus of patients with DD and in that of controls. Expression of the inflammatory cytokines tumor necrosis factor-alpha and interleukin-6 was quantified using qPCR, and infiltration of CD3+ lymphocytes was determined using immunohistochemistry. Results: Expression of S100 beta was increased in the submucosal and myenteric plexus of patients with DD compared with that in controls, whereas expression of other glial factors remained unchanged. This increased expression of S100 beta was correlated to CD3+ lymphocytic infiltrates in patients with DD, whereas no correlation was observed in controls. Conclusions: DD is associated with limited but significant alterations of the enteric glial network. The increased expression of S100 beta is associated with a persistent low-grade inflammation reported in patients with DD, further emphasizing the role of EGCs in intestinal inflammation.
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