Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic Itch

Itch is a clinical problem that leaves many sufferers insufficiently treated, with over 20 million cases in the United States. This is due to incomplete understanding of its molecular, cellular, and cell-to-cell signaling mechanisms. Transient receptor potential (TRP) ion channels are involved in se...

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Main Authors: Qiaojuan Zhang, Gwendolyn Henry, Yong Chen
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/14/7591
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spelling doaj-88bf8165f793482fba6d9f47b55359382021-07-23T13:46:27ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-07-01227591759110.3390/ijms22147591Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic ItchQiaojuan Zhang0Gwendolyn Henry1Yong Chen2Department of Neurology, Duke University, Durham, NC 27710, USADepartment of Neurology, Duke University, Durham, NC 27710, USADepartment of Neurology, Duke University, Durham, NC 27710, USAItch is a clinical problem that leaves many sufferers insufficiently treated, with over 20 million cases in the United States. This is due to incomplete understanding of its molecular, cellular, and cell-to-cell signaling mechanisms. Transient receptor potential (TRP) ion channels are involved in several sensory modalities including pain, vision, taste, olfaction, hearing, touch, and thermosensation, as well as itch. Relative to the extensive studies on TRPV1 and TRPA1 ion channels in itch modulation, TRPV4 has received relatively little research attention and its mechanisms have remained poorly understood until recently. TRPV4 is expressed in ganglion sensory neurons and a variety of skin cells. Growing evidence in the past few years strongly suggests that TRPV4 in these cells contributes to acute and chronic disease-associated itch. This review focuses on the current experimental evidence involving TRPV4 in itch under pathophysiological conditions and discusses its possible cellular and molecular mechanisms.https://www.mdpi.com/1422-0067/22/14/7591TRPV4itchkeratinocytessensory neuronspruritogen
collection DOAJ
language English
format Article
sources DOAJ
author Qiaojuan Zhang
Gwendolyn Henry
Yong Chen
spellingShingle Qiaojuan Zhang
Gwendolyn Henry
Yong Chen
Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic Itch
International Journal of Molecular Sciences
TRPV4
itch
keratinocytes
sensory neurons
pruritogen
author_facet Qiaojuan Zhang
Gwendolyn Henry
Yong Chen
author_sort Qiaojuan Zhang
title Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic Itch
title_short Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic Itch
title_full Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic Itch
title_fullStr Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic Itch
title_full_unstemmed Emerging Role of Transient Receptor Potential Vanilloid 4 (TRPV4) Ion Channel in Acute and Chronic Itch
title_sort emerging role of transient receptor potential vanilloid 4 (trpv4) ion channel in acute and chronic itch
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-07-01
description Itch is a clinical problem that leaves many sufferers insufficiently treated, with over 20 million cases in the United States. This is due to incomplete understanding of its molecular, cellular, and cell-to-cell signaling mechanisms. Transient receptor potential (TRP) ion channels are involved in several sensory modalities including pain, vision, taste, olfaction, hearing, touch, and thermosensation, as well as itch. Relative to the extensive studies on TRPV1 and TRPA1 ion channels in itch modulation, TRPV4 has received relatively little research attention and its mechanisms have remained poorly understood until recently. TRPV4 is expressed in ganglion sensory neurons and a variety of skin cells. Growing evidence in the past few years strongly suggests that TRPV4 in these cells contributes to acute and chronic disease-associated itch. This review focuses on the current experimental evidence involving TRPV4 in itch under pathophysiological conditions and discusses its possible cellular and molecular mechanisms.
topic TRPV4
itch
keratinocytes
sensory neurons
pruritogen
url https://www.mdpi.com/1422-0067/22/14/7591
work_keys_str_mv AT qiaojuanzhang emergingroleoftransientreceptorpotentialvanilloid4trpv4ionchannelinacuteandchronicitch
AT gwendolynhenry emergingroleoftransientreceptorpotentialvanilloid4trpv4ionchannelinacuteandchronicitch
AT yongchen emergingroleoftransientreceptorpotentialvanilloid4trpv4ionchannelinacuteandchronicitch
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