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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Main Authors: Chengcheng Huang, Fumin Lu, Ping Li, Cheng Cao, Zijing Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-06-01
Series:Frontiers in Molecular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fnmol.2017.00205/full
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spelling doaj-14a5b73dbf5447e88bb727fee66acbc82020-11-24T23:51:57ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992017-06-011010.3389/fnmol.2017.00205261372Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain SensationsChengcheng Huang0Fumin Lu1Ping Li2Cheng Cao3Zijing Liu4Beijing Institute of BiotechnologyBeijing, ChinaSchool of Life Sciences, Anhui Agricultural UniversityHefei, ChinaBeijing Institute of BiotechnologyBeijing, ChinaBeijing Institute of BiotechnologyBeijing, ChinaBeijing Institute of BiotechnologyBeijing, ChinaItch, 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, Tlx3F/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 Tlx3F/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.http://journal.frontiersin.org/article/10.3389/fnmol.2017.00205/fullTlx3itchpainpruriceptorTRPV1dorsal root ganglion
collection DOAJ
language English
format Article
sources DOAJ
author Chengcheng Huang
Fumin Lu
Ping Li
Cheng Cao
Zijing Liu
spellingShingle Chengcheng Huang
Fumin Lu
Ping Li
Cheng Cao
Zijing Liu
Tlx3 Function in the Dorsal Root Ganglion is Pivotal to Itch and Pain Sensations
Frontiers in Molecular Neuroscience
Tlx3
itch
pain
pruriceptor
TRPV1
dorsal root ganglion
author_facet Chengcheng Huang
Fumin Lu
Ping Li
Cheng Cao
Zijing Liu
author_sort Chengcheng Huang
title 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_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_sort tlx3 function in the dorsal root ganglion is pivotal to itch and pain sensations
publisher Frontiers Media S.A.
series Frontiers in Molecular Neuroscience
issn 1662-5099
publishDate 2017-06-01
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, Tlx3F/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 Tlx3F/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.
topic Tlx3
itch
pain
pruriceptor
TRPV1
dorsal root ganglion
url http://journal.frontiersin.org/article/10.3389/fnmol.2017.00205/full
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