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Protease-activated receptors: the role of cell-surface proteolysis in signalling

Cottrell, G. S., Coelho, A. M. and Bunnett, N. W. (2002) Protease-activated receptors: the role of cell-surface proteolysis in signalling. Essays in Biochemistry, 38. pp. 169-183. ISSN 0071-1365

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Official URL: http://essays.biochemistry.org/bsessays/038/bse038...

Abstract/Summary

Certain extracellular proteases, derived from the circulation and inflammatory cells, can specifically cleave and trigger protease-activated receptors (PARs), a small, but important, sub-group of the G-protein-coupled receptor super-family. Four PARs have been cloned and they all share the same basic mechanism of activation: proteases cleave at a specific site within the extracellular N-terminus to expose a new N-terminal tethered ligand domain, which binds to and thereby activates the cleaved receptor. Thrombin activates PAR1, PAR3 and PAR4, trypsin activates PAR2 and PAR4, and mast cell tryptase activates PAR2 in this manner. Activated PARs couple to signalling cascades that affect cell shape, secretion, integrin activation, metabolic responses, transcriptional responses and cell motility. PARs are 'single-use' receptors: proteolytic activation is irreversible and the cleaved receptors are degraded in lysosomes. Thus, PARs play important roles in 'emergency situations', such as trauma and inflammation. The availability of selective agonists and antagonists of protease inhibitors and of genetic models has generated evidence to suggests that proteases and their receptors play important roles in coagulation, inflammation, pain, healing and protection. Therefore, selective antagonists or agonists of these receptors may be useful therapeutic agents for the treatment of human diseases.

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:30287
Uncontrolled Keywords:Animals Cell Membrane/*metabolism Humans Inflammation Models, Biological Protein Processing, Post-Translational Receptor, PAR-1 Receptor, PAR-2 Receptors, Thrombin/*metabolism/*physiology *Signal Transduction
Additional Information:Cottrell, Graeme S Coelho, Anne-Marie Bunnett, Nigel W DK39957/DK/NIDDK NIH HHS/ DK43207/DK/NIDDK NIH HHS/ DK57840/DK/NIDDK NIH HHS/ England Essays Biochem. 2002;38:169-83.
Publisher:Portland Press Ltd

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