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NF‐κB is activated in oesophageal fibroblasts in response to a paracrine signal generated by acid‐exposed primary oesophageal squamous cells
Author(s) -
Green Nicola H.,
Huang Qizhi,
Corfe Bernard M.,
Bury Jonathan P.,
MacNeil Sheila
Publication year - 2011
Publication title -
international journal of experimental pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.671
H-Index - 72
eISSN - 1365-2613
pISSN - 0959-9673
DOI - 10.1111/j.1365-2613.2011.00778.x
Subject(s) - stromal cell , paracrine signalling , nf κb , cancer research , cell culture , chemistry , biology , microbiology and biotechnology , signal transduction , receptor , biochemistry , genetics
Summary Oesophageal exposure to duodenogastro‐oesophageal refluxate leads to reflux oesophagitis and is implicated in the development of Barrett’s metaplasia (BM). NF‐κB signalling in epithelial cells is associated with the activation of transcription factors believed to be central to BM development, whilst NF‐κB activation in fibroblasts plays a critical role in matrix remodelling. Our aim was to study the effects of acid exposure on NF‐κB activation in primary human oesophageal fibroblasts (HOFs) and primary and immortalized oesophageal squames and to investigate any epithelial/stromal interactions in the response of these cells to acid. Primary HOFs and primary and immortalized oesophageal epithelial cells were exposed to acid (pH 7 – pH 4 ≤ 120 min) in single or pulsed treatments. Conditioned medium from epithelial cells following acid exposure was also applied to fibroblasts. Cell viability was determined by MTT‐ESTA. NF‐κB activation was determined by cellular localization of NF‐κB/p65 visualized by immunofluorescence. Conditioned medium from oesophageal epithelial cells, subjected to pH 5 pulsatile exposure, activated NF‐κB in fibroblasts, with some inter‐patient variability, but these conditions did not directly activate NF‐κB in the epithelial cells themselves. Significant NF‐κB activation was seen in the epithelial cells but only with greater acidity and exposure times (pH 4, 60–120 min). Our findings show that acid exposure can cause indirect activation of stromal cells by epithelial–stromal interactions. This may contribute to the pathogenesis of oesophageal diseases, and the inter‐patient variability may go some way to explain why some patients with reflux oesophagitis develop BM and others do not.