Redefining the concept of protease-activated receptors: cathepsin S evokes itch via activation of Mrgprs

Sensory neurons expressing Mas-related G protein coupled receptors (Mrgprs) mediate histamine-independent itch. We show that the cysteine protease cathepsin S activates MrgprC11 and evokes receptor-dependent scratching in mice. In contrast to its activation of conventional protease-activated receptors, cathepsin S mediated activation of MrgprC11 did not involve the generation of a tethered ligand. We demonstrate further that different cysteine proteases selectively activate specific mouse and human Mrgpr family members. This expansion of our understanding by which proteases interact with GPCRs redefines the concept of what constitutes a protease-activated receptor. The findings also implicate proteases as ligands to members of this orphan receptor family while providing new insights into how cysteine proteases contribute to itch.

[1]  David J. Anderson,et al.  A Diverse Family of GPCRs Expressed in Specific Subsets of Nociceptive Sensory Neurons , 2001, Cell.

[2]  J. Vilardaga ENDOSOMAL GENERATION OF cAMP in GPCR SIGNALING , 2014, Nature chemical biology.

[3]  S. Bevan,et al.  Inhibition of spinal microglial cathepsin S for the reversal of neuropathic pain , 2007, Proceedings of the National Academy of Sciences.

[4]  E. Lerner,et al.  Plant cysteine proteases that evoke itch activate protease‐activated receptors , 2010, The British journal of dermatology.

[5]  G. Bilbe,et al.  Molecular cloning of human cDNA for cathepsin K: novel cysteine proteinase predominantly expressed in bone. , 1995, Biochemical and biophysical research communications.

[6]  D. Banville,et al.  Proenkephalin A gene products activate a new family of sensory neuron–specific GPCRs , 2002, Nature Neuroscience.

[7]  P. Nurden,et al.  The Cleaved Peptide of PAR1 Results in a Redistribution of the Platelet Surface GPIb-IX-V Complex to the Surface-Connected Canalicular System , 2000, Thrombosis and Haemostasis.

[8]  Xinzhong Dong,et al.  TRPA1 is required for histamine-independent, Mas-related G protein-coupled receptor-mediated itch , 2011, Nature Neuroscience.

[9]  K. Hoffmann,et al.  Upregulation of cathepsin S in psoriatic keratinocytes , 2009, Experimental dermatology.

[10]  Hollenberg Proteinases and signalling - to PAR or Bogey: Pathophysiological and therapeutic implications via PARs and more , 2007 .

[11]  Ping-Chang Yang,et al.  Mast Cell Tryptase Controls Paracellular Permeability of the Intestine , 2005, Journal of Biological Chemistry.

[12]  M. Grossmann,et al.  G Protein-coupled Receptors , 1998, The Journal of Biological Chemistry.

[13]  M. Bogyo,et al.  Cathepsin S is activated during colitis and causes visceral hyperalgesia by a PAR2-dependent mechanism in mice. , 2011, Gastroenterology.

[14]  R. LaMotte,et al.  Mechanisms of Itch Evoked by β-Alanine , 2012, The Journal of Neuroscience.

[15]  T. Lotti,et al.  Itch in psoriasis: epidemiology, clinical aspects and treatment options , 2009, Clinical, cosmetic and investigational dermatology.

[16]  M. von Zastrow,et al.  G Protein-coupled Receptor (GPCR) Signaling via Heterotrimeric G Proteins from Endosomes* , 2015, The Journal of Biological Chemistry.

[17]  Xinzhong Dong,et al.  The Distinct Roles of Two GPCRs, MrgprC11 and PAR2, in Itch and Hyperalgesia , 2011, Science Signaling.

[18]  E. Lerner,et al.  Cathepsin S Signals via PAR2 and Generates a Novel Tethered Ligand Receptor Agonist , 2014, PloS one.

[19]  R. Dubner,et al.  Central Terminal Sensitization of TRPV1 by Descending Serotonergic Facilitation Modulates Chronic Pain , 2014, Neuron.

[20]  김나리,et al.  Overexpression of cathepsin S induces chronic atopic dermatitis in mice , 2011 .

[21]  HighWire Press The journal of neuroscience : the official journal of the Society for Neuroscience. , 1981 .

[22]  M. Pellegrino,et al.  The Epithelial Cell-Derived Atopic Dermatitis Cytokine TSLP Activates Neurons to Induce Itch , 2013, Cell.

[23]  J. Wallace,et al.  Agonists of proteinase-activated receptor 2 induce inflammation by a neurogenic mechanism , 2000, Nature Medicine.

[24]  C. Flordellis,et al.  Parstatin, the Cleaved Peptide on Proteinase-Activated Receptor 1 Activation, Is a Potent Inhibitor of Angiogenesis , 2009, Journal of Pharmacology and Experimental Therapeutics.

[25]  Erik Lindström,et al.  Cathepsin S Causes Inflammatory Pain via Biased Agonism of PAR2 and TRPV4* , 2014, The Journal of Biological Chemistry.

[26]  R. LaMotte,et al.  Cathepsin S elicits itch and signals via protease-activated receptors. , 2010, The Journal of investigative dermatology.

[27]  R. LaMotte,et al.  BAM8–22 Peptide Produces Itch and Nociceptive Sensations in Humans Independent of Histamine Release , 2011, The Journal of Neuroscience.

[28]  Bonnie F. Sloane,et al.  Cysteine cathepsins: multifunctional enzymes in cancer , 2006, Nature Reviews Cancer.

[29]  V. Wheaton,et al.  Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activation , 1991, Cell.

[30]  Robert H. LaMotte,et al.  Cowhage-Evoked Itch Is Mediated by a Novel Cysteine Protease: A Ligand of Protease-Activated Receptors , 2008, The Journal of Neuroscience.

[31]  David J. Anderson,et al.  Sensory Neuron-Specific GPCR Mrgprs Are Itch Receptors Mediating Chloroquine-Induced Pruritus , 2009, Cell.

[32]  N. Schork,et al.  Pruritus in psoriasis. A prospective study of some psychiatric and dermatologic correlates. , 1988, Archives of dermatology.

[33]  M. Bayliss,et al.  The impact of itch symptoms in psoriasis: results from physician interviews and patient focus groups , 2009, Health and quality of life outcomes.

[34]  R. LaMotte,et al.  Behavioral differentiation between itch and pain in mouse , 2008, PAIN.

[35]  M. Hollenberg,et al.  Proteinases and signalling: pathophysiological and therapeutic implications via PARs and more , 2008, British journal of pharmacology.

[36]  Christopher M. Tan,et al.  Genetic and pharmacological evaluation of cathepsin s in a mouse model of asthma. , 2011, American journal of respiratory cell and molecular biology.

[37]  A. Ray,et al.  Cysteine cathepsin S as an immunomodulatory target: present and future trends , 2008, Expert opinion on therapeutic targets.

[38]  Alex Bateman,et al.  MEROPS: the database of proteolytic enzymes, their substrates and inhibitors , 2011, Nucleic Acids Res..