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Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations

Itch, a sensation eliciting a desire to scratch, is distinct from but not completely independent of pain. Inspiring achievements have been made in the characterization of itch-related receptors and neurotransmitters, but the molecular mechanisms controlling the development of pruriceptors remain poo...

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Autores principales: Huang, Chengcheng, Lu, Fumin, Li, Ping, Cao, Cheng, Liu, Zijing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487456/
https://www.ncbi.nlm.nih.gov/pubmed/28701920
http://dx.doi.org/10.3389/fnmol.2017.00205
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author Huang, Chengcheng
Lu, Fumin
Li, Ping
Cao, Cheng
Liu, Zijing
author_facet Huang, Chengcheng
Lu, Fumin
Li, Ping
Cao, Cheng
Liu, Zijing
author_sort Huang, Chengcheng
collection PubMed
description Itch, a sensation eliciting a desire to scratch, is distinct from but not completely independent of pain. Inspiring achievements have been made in the characterization of itch-related receptors and neurotransmitters, but the molecular mechanisms controlling the development of pruriceptors remain poorly understood. Here, our RNAseq and in situ hybridization data show that the transcription factor Tlx3 is required for the expression of a majority of itch-related molecules in the dorsal root ganglion (DRG). As a result, Tlx3(F/F);Nav1.8-cre mice exhibit significantly attenuated acute and dry skin-induced chronic itch. Furthermore, our study indicates that TRPV1 plays a pivotal role in the chronic itch evoked by dry skin and allergic contact dermatitis (ACD). The mutants also display impaired response to cold and inflammatory pain and elevated response to capsaicin, whereas the responses to acute mechanical, thermal stimuli and neuropathic pain remain normal. In Tlx3(F/F);Nav1.8-cre mice, TRPV1 is derepressed and expands predominantly into IB4(+) non-peptidergic (NP) neurons. Collectively, our data reveal a molecular mechanism in regulating the development of pruriceptors and controlling itch and pain sensations.
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spelling pubmed-54874562017-07-12 Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations Huang, Chengcheng Lu, Fumin Li, Ping Cao, Cheng Liu, Zijing Front Mol Neurosci Neuroscience Itch, a sensation eliciting a desire to scratch, is distinct from but not completely independent of pain. Inspiring achievements have been made in the characterization of itch-related receptors and neurotransmitters, but the molecular mechanisms controlling the development of pruriceptors remain poorly understood. Here, our RNAseq and in situ hybridization data show that the transcription factor Tlx3 is required for the expression of a majority of itch-related molecules in the dorsal root ganglion (DRG). As a result, Tlx3(F/F);Nav1.8-cre mice exhibit significantly attenuated acute and dry skin-induced chronic itch. Furthermore, our study indicates that TRPV1 plays a pivotal role in the chronic itch evoked by dry skin and allergic contact dermatitis (ACD). The mutants also display impaired response to cold and inflammatory pain and elevated response to capsaicin, whereas the responses to acute mechanical, thermal stimuli and neuropathic pain remain normal. In Tlx3(F/F);Nav1.8-cre mice, TRPV1 is derepressed and expands predominantly into IB4(+) non-peptidergic (NP) neurons. Collectively, our data reveal a molecular mechanism in regulating the development of pruriceptors and controlling itch and pain sensations. Frontiers Media S.A. 2017-06-28 /pmc/articles/PMC5487456/ /pubmed/28701920 http://dx.doi.org/10.3389/fnmol.2017.00205 Text en Copyright © 2017 Huang, Lu, Li, Cao and Liu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Huang, Chengcheng
Lu, Fumin
Li, Ping
Cao, Cheng
Liu, Zijing
Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations
title Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations
title_full Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations
title_fullStr Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations
title_full_unstemmed Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations
title_short Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations
title_sort tlx3 function in the dorsal root ganglion is pivotal to itch and pain sensations
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487456/
https://www.ncbi.nlm.nih.gov/pubmed/28701920
http://dx.doi.org/10.3389/fnmol.2017.00205
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