Abstract
Background:
Eosinophils reside in normal gastrointestinal tracts and increase during disease states. Receptors for eosinophil-derived granule proteins (EDGPs) have not been identified, but highly cationic molecules, similar to eosinophil proteins, bind extracellular calcium–sensing receptors (CaSRs). We hypothesized that stimulation of CaSRs by eosinophil proteins activates epithelial cells.
Methods:
Caco2 intestinal epithelial cells, AML14.3D10 eosinophils, wild-type (WT) human embryonic kidney 293 (HEK293) cells not expressing CaSRs (HEK-WT), and CaSR-transfected HEK293 cells (HEK-CaSR) were stimulated with an eosinophil protein analog poly-L-arginine (PA) and phosphorylated extracellular signal–regulated kinase (pERK)1 and pERK2 were measured. Functional activation was measured with collagen lattice contraction assays.
Results:
Coculture of Caco2 cells with AML14.3D10 eosinophils augmented lattice contraction as compared with lattices containing Caco2 cells alone. PA stimulation of Caco2 lattices augmented contraction. HEK-CaSR stimulation with PA or Ca2+ resulted in greater pERK activation than that of stimulated HEK-WT cells. PA stimulated greater HEK-CaSR lattice contraction than unstimulated lattices. Contraction of PA-stimulated and PA-unstimulated HEK-WT lattices did not differ.
Conclusion:
Exposure of intestinal epithelia to the EDGP analog PA stimulates CaSR-dependent ERK phosphorylation and epithelial-mediated collagen lattice contraction. We speculate that EDGP release within the epithelial layers activates the CaSR receptor, leading to matrix contraction and tissue fibrosis.
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Acknowledgements
The authors acknowledge the excellent technical assistance and expertise of Jonathan Phillips, Joanne Masterson, and Raina Ficherova and the generous advice and support of Sean P. Colgan. R.J.M. holds the Canada Research Chair in GI Cell Physiology.
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Ngo, P., MacLeod, R., Mukkada, V. et al. Epithelial calcium–sensing receptor activation by eosinophil granule protein analog stimulates collagen matrix contraction. Pediatr Res 73, 414–419 (2013). https://doi.org/10.1038/pr.2012.198
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DOI: https://doi.org/10.1038/pr.2012.198
