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Mast cell tryptase and proteinase-activated receptor 2 induce hyperexcitability of guinea-pig submucosal neurons

Reed, D. E., Barajas-Lopez, C., Cottrell, G. S., Velazquez-Rocha, S., Dery, O., Grady, E. F., Bunnett, N. W. and Vanner, S. J. (2003) Mast cell tryptase and proteinase-activated receptor 2 induce hyperexcitability of guinea-pig submucosal neurons. Journal of Physiology, 547 (2). pp. 531-542. ISSN 0022-3751

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To link to this item DOI: 10.1113/jphysiol.2002.032011

Abstract/Summary

Mast cells that are in close proximity to autonomic and enteric nerves release several mediators that cause neuronal hyperexcitability. This study examined whether mast cell tryptase evokes acute and long-term hyperexcitability in submucosal neurons from the guinea-pig ileum by activating proteinase-activated receptor 2 (PAR2) on these neurons. We detected the expression of PAR2 in the submucosal plexus using RT-PCR. Most submucosal neurons displayed PAR2 immunoreactivity, including those colocalizing VIP. Brief (minutes) application of selective PAR2 agonists, including trypsin, the activating peptide SL-NH2 and mast cell tryptase, evoked depolarizations of the submucosal neurons, as measured with intracellular recording techniques. The membrane potential returned to resting values following washout of agonists, but most neurons were hyperexcitable for the duration of recordings (> 30 min-hours) and exhibited an increased input resistance and amplitude of fast EPSPs. Trypsin, in the presence of soybean trypsin inhibitor, and the reverse sequence of the activating peptide (LR-NH2) had no effect on neuronal membrane potential or long-term excitability. Degranulation of mast cells in the presence of antagonists of established excitatory mast cell mediators (histamine, 5-HT, prostaglandins) also caused depolarization, and following washout of antigen, long-term excitation was observed. Mast cell degranulation resulted in the release of proteases, which desensitized neurons to other agonists of PAR2. Our results suggest that proteases from degranulated mast cells cleave PAR2 on submucosal neurons to cause acute and long-term hyperexcitability. This signalling pathway between immune cells and neurons is a previously unrecognized mechanism that could contribute to chronic alterations in visceral function.

Item Type:Article
Refereed:Yes
Divisions:Faculty of Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy > Division of Pharmacology
No Reading authors. Back catalogue items
ID Code:30285
Uncontrolled Keywords:Animals Cell Degranulation Electrophysiology Guinea Pigs Ileum/innervation Immunohistochemistry Lactoglobulins/pharmacology Mast Cells/*metabolism/physiology Neurons/drug effects/*physiology Oligopeptides/pharmacology Receptor, PAR-2 Receptors, Thrombin/agonists/*metabolism Reverse Transcriptase Polymerase Chain Reaction Serine Endopeptidases/*metabolism Submucous Plexus/cytology/drug effects/*physiology Synapses/drug effects/physiology Tissue Distribution Trypsin/pharmacology Tryptases Vasoactive Intestinal Peptide/metabolism
Publisher:Wiley-Blackwell

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