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Identification of a bilirubin receptor that may mediate a component of cholestatic itch

Various pathologic conditions result in jaundice, a yellowing of the skin due to a buildup of bilirubin. Patients with jaundice commonly report experiencing an intense non-histaminergic itch. Despite this association, the pruritogenic capacity of bilirubin itself has not been described, and no bilir...

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Autores principales: Meixiong, James, Vasavda, Chirag, Green, Dustin, Zheng, Qin, Qi, Lijun, Kwatra, Shawn G, Hamilton, James P, Snyder, Solomon H, Dong, Xinzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368403/
https://www.ncbi.nlm.nih.gov/pubmed/30657454
http://dx.doi.org/10.7554/eLife.44116
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author Meixiong, James
Vasavda, Chirag
Green, Dustin
Zheng, Qin
Qi, Lijun
Kwatra, Shawn G
Hamilton, James P
Snyder, Solomon H
Dong, Xinzhong
author_facet Meixiong, James
Vasavda, Chirag
Green, Dustin
Zheng, Qin
Qi, Lijun
Kwatra, Shawn G
Hamilton, James P
Snyder, Solomon H
Dong, Xinzhong
author_sort Meixiong, James
collection PubMed
description Various pathologic conditions result in jaundice, a yellowing of the skin due to a buildup of bilirubin. Patients with jaundice commonly report experiencing an intense non-histaminergic itch. Despite this association, the pruritogenic capacity of bilirubin itself has not been described, and no bilirubin receptor has been identified. Here, we demonstrate that pathophysiologic levels of bilirubin excite peripheral itch sensory neurons and elicit pruritus through MRGPRs, a family of G-protein coupled receptors expressed in primary sensory neurons. Bilirubin binds and activates two MRGPRs, mouse MRGPRA1 and human MRGPRX4. In two mouse models of pathologic hyperbilirubinemia, we show that genetic deletion of either Mrgpra1 or Blvra, the gene that encodes the bilirubin-producing enzyme biliverdin reductase, attenuates itch. Similarly, plasma isolated from hyperbilirubinemic patients evoked itch in wild-type animals but not Mrgpra1(-/-) animals. Removing bilirubin decreased the pruritogenic capacity of patient plasma. Based on these data, targeting MRGPRs is a promising strategy for alleviating jaundice-associated itch.
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spelling pubmed-63684032019-02-11 Identification of a bilirubin receptor that may mediate a component of cholestatic itch Meixiong, James Vasavda, Chirag Green, Dustin Zheng, Qin Qi, Lijun Kwatra, Shawn G Hamilton, James P Snyder, Solomon H Dong, Xinzhong eLife Neuroscience Various pathologic conditions result in jaundice, a yellowing of the skin due to a buildup of bilirubin. Patients with jaundice commonly report experiencing an intense non-histaminergic itch. Despite this association, the pruritogenic capacity of bilirubin itself has not been described, and no bilirubin receptor has been identified. Here, we demonstrate that pathophysiologic levels of bilirubin excite peripheral itch sensory neurons and elicit pruritus through MRGPRs, a family of G-protein coupled receptors expressed in primary sensory neurons. Bilirubin binds and activates two MRGPRs, mouse MRGPRA1 and human MRGPRX4. In two mouse models of pathologic hyperbilirubinemia, we show that genetic deletion of either Mrgpra1 or Blvra, the gene that encodes the bilirubin-producing enzyme biliverdin reductase, attenuates itch. Similarly, plasma isolated from hyperbilirubinemic patients evoked itch in wild-type animals but not Mrgpra1(-/-) animals. Removing bilirubin decreased the pruritogenic capacity of patient plasma. Based on these data, targeting MRGPRs is a promising strategy for alleviating jaundice-associated itch. eLife Sciences Publications, Ltd 2019-01-21 /pmc/articles/PMC6368403/ /pubmed/30657454 http://dx.doi.org/10.7554/eLife.44116 Text en © 2019, Meixiong et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Meixiong, James
Vasavda, Chirag
Green, Dustin
Zheng, Qin
Qi, Lijun
Kwatra, Shawn G
Hamilton, James P
Snyder, Solomon H
Dong, Xinzhong
Identification of a bilirubin receptor that may mediate a component of cholestatic itch
title Identification of a bilirubin receptor that may mediate a component of cholestatic itch
title_full Identification of a bilirubin receptor that may mediate a component of cholestatic itch
title_fullStr Identification of a bilirubin receptor that may mediate a component of cholestatic itch
title_full_unstemmed Identification of a bilirubin receptor that may mediate a component of cholestatic itch
title_short Identification of a bilirubin receptor that may mediate a component of cholestatic itch
title_sort identification of a bilirubin receptor that may mediate a component of cholestatic itch
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368403/
https://www.ncbi.nlm.nih.gov/pubmed/30657454
http://dx.doi.org/10.7554/eLife.44116
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