Alterations in junctional proteins, inflammatory mediators and extracellular matrix molecules in eosinophilic esophagitis

作者：Abdulnour Nakhoul Solange M^*; Al Tawil Youhanna; Gyftopoulos Alex A; Brown Karen L; Hansen Molly; Butcher Kathy F; Eidelwein Alexandra P; Noel Robert A; Rabon Edd; Posta Allison; Nakhoul Nazih L

来源：Clinical Immunology, 2013, 148(2): 265-278.

DOI：10.1016/j.clim.2013.05.004

• Cytokines
• Claudin-1
• Occludin
• Vimentin
• E-cadherin
• Inflammation

Eosinophilic esophagitis (EoE), an inflammatory atopic disease of the esophagus, causes massive eosinophil infiltration, basal cell hyperplasia, and sub-epithelial fibrosis. To elucidate cellular and molecular factors involved in esophageal tissue damage and remodeling, we examined pinch biopsies from EoE and normal pediatric patients. An inflammation gene array confirmed that eotaxin-3, its receptor CCR3 and interleukins IL-13 and IL-5 were upregulated. An extracellular matrix (ECM) gene array revealed upregulation of CD44 & CD54, and of ECM proteases (ADAMTS1 & MMP14). A cytokine antibody array showed a marked decrease in IL-1 alpha and IL-1 receptor antagonist and an increase in eotaxin-2 and epidermal growth factor. Western analysis indicated reduced expression of intercellular junction proteins, E-cadherin and claudin-1 and increased expression of occludin and vimentin. We have identified a number of novel genes and proteins whose expression is altered in EoE. These findings provide new insights into the molecular mechanisms of the disease.

• 出版日期2013-8