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ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus
Recent studies have shown that ZBTB20, a zinc-finger protein containing transcription factor, is highly expressed in small-diameter primary sensory neurons in mice, and modulates pain through regulating TRP channels. However, whether ZBTB20 regulates itch sensation has not been demonstrated. In this...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969640/ https://www.ncbi.nlm.nih.gov/pubmed/33748159 http://dx.doi.org/10.3389/fmed.2021.626554 |
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author | Jia, Xin Dai, Meng-Han Ren, An-Jing Wang, Ting-Ting Zhang, Weiping J. Zhang, Ling |
author_facet | Jia, Xin Dai, Meng-Han Ren, An-Jing Wang, Ting-Ting Zhang, Weiping J. Zhang, Ling |
author_sort | Jia, Xin |
collection | PubMed |
description | Recent studies have shown that ZBTB20, a zinc-finger protein containing transcription factor, is highly expressed in small-diameter primary sensory neurons in mice, and modulates pain through regulating TRP channels. However, whether ZBTB20 regulates itch sensation has not been demonstrated. In this study, small-diameter primary sensory neuron-specific ZBTB20 knockout (PN-ZB20KO) mice were used to investigate the role of ZBTB20 in the regulation of itch sensation. First, both histamine-dependent and non-histamine-dependent itch behaviors induced by injection of histamine and chloroquine (CQ) into the cheek were significantly diminished in PN-ZB20KO mice. Second, double immunohistochemistry showed that ZBTB20 was mainly expressed in CGRP-labeled small peptidergic neurons and was expressed at low levels in IB4-labeled small non-peptidergic and NF200-labeled large neurons in the trigeminal ganglia (TG). ZBTB20 was also expressed in most TRPV1(+) and TRPA1(+) neurons and to a lesser extent in TRPM8(+) neurons in the TG. Furthermore, cheek injection of histamine and CQ enhanced the mRNA expression of TRPV1 and TRPA1 but not TRPM8 in the TG. Moreover, TRPV1 and TRPA1 knockout (KO) mice exhibited attenuation of itch behavior induced by histamine and CQ, respectively. Finally, silencing endogenous ZBTB20 with recombinant lentivirus expressing a short hairpin RNA against ZBTB20 (LV-shZBTB20) in TG neurons attenuated histamine- and non-histamine-induced itch and downregulated TRP channels in the TG. Our study suggests that ZBTB20 plays an important role in mediating itch in small primary sensory neurons. |
format | Online Article Text |
id | pubmed-7969640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79696402021-03-19 ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus Jia, Xin Dai, Meng-Han Ren, An-Jing Wang, Ting-Ting Zhang, Weiping J. Zhang, Ling Front Med (Lausanne) Medicine Recent studies have shown that ZBTB20, a zinc-finger protein containing transcription factor, is highly expressed in small-diameter primary sensory neurons in mice, and modulates pain through regulating TRP channels. However, whether ZBTB20 regulates itch sensation has not been demonstrated. In this study, small-diameter primary sensory neuron-specific ZBTB20 knockout (PN-ZB20KO) mice were used to investigate the role of ZBTB20 in the regulation of itch sensation. First, both histamine-dependent and non-histamine-dependent itch behaviors induced by injection of histamine and chloroquine (CQ) into the cheek were significantly diminished in PN-ZB20KO mice. Second, double immunohistochemistry showed that ZBTB20 was mainly expressed in CGRP-labeled small peptidergic neurons and was expressed at low levels in IB4-labeled small non-peptidergic and NF200-labeled large neurons in the trigeminal ganglia (TG). ZBTB20 was also expressed in most TRPV1(+) and TRPA1(+) neurons and to a lesser extent in TRPM8(+) neurons in the TG. Furthermore, cheek injection of histamine and CQ enhanced the mRNA expression of TRPV1 and TRPA1 but not TRPM8 in the TG. Moreover, TRPV1 and TRPA1 knockout (KO) mice exhibited attenuation of itch behavior induced by histamine and CQ, respectively. Finally, silencing endogenous ZBTB20 with recombinant lentivirus expressing a short hairpin RNA against ZBTB20 (LV-shZBTB20) in TG neurons attenuated histamine- and non-histamine-induced itch and downregulated TRP channels in the TG. Our study suggests that ZBTB20 plays an important role in mediating itch in small primary sensory neurons. Frontiers Media S.A. 2021-03-04 /pmc/articles/PMC7969640/ /pubmed/33748159 http://dx.doi.org/10.3389/fmed.2021.626554 Text en Copyright © 2021 Jia, Dai, Ren, Wang, Zhang and Zhang. 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) and the copyright owner(s) 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 | Medicine Jia, Xin Dai, Meng-Han Ren, An-Jing Wang, Ting-Ting Zhang, Weiping J. Zhang, Ling ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus |
title | ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus |
title_full | ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus |
title_fullStr | ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus |
title_full_unstemmed | ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus |
title_short | ZBTB20 in Nociceptive Neurons of the Trigeminal Ganglia Regulates Pruritus |
title_sort | zbtb20 in nociceptive neurons of the trigeminal ganglia regulates pruritus |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969640/ https://www.ncbi.nlm.nih.gov/pubmed/33748159 http://dx.doi.org/10.3389/fmed.2021.626554 |
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