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The calcium-activated chloride channel anoctamin 1 acts as a heat sensor in nociceptive neurons

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dc.contributor.authorCho, Hawon-
dc.contributor.authorYang, Young Duk-
dc.contributor.authorLee, Jesun-
dc.contributor.authorLee, Byeongjoon-
dc.contributor.authorKim, Tahnbee-
dc.contributor.authorJang, Yong woo-
dc.contributor.authorBack, Seung Keun-
dc.contributor.authorNa, Heung Sik-
dc.contributor.authorHarfe, Brian D.-
dc.contributor.authorWang, Fan-
dc.contributor.authorRaouf, Ramin-
dc.contributor.authorWood, John N.-
dc.contributor.authorOh, Uhtaek-
dc.date.accessioned2022-07-16T14:49:19Z-
dc.date.available2022-07-16T14:49:19Z-
dc.date.created2021-05-13-
dc.date.issued2012-06-
dc.identifier.issn1097-6256-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/165290-
dc.description.abstractNociceptors are a subset of small primary afferent neurons that respond to noxious chemical, thermal and mechanical stimuli. Ion channels in nociceptors respond differently to noxious stimuli and generate electrical signals in different ways. Anoctamin 1 (ANO1 also known as TMEM16A) is a Ca2+-activated chloride channel that is essential for numerous physiological functions. We found that ANO1 was activated by temperatures over 44 degrees C with steep heat sensitivity. ANO1 was expressed in small sensory neurons and was highly colocalized with nociceptor markers, which suggests that it may be involved in nociception. Application of heat ramps to dorsal root ganglion (DRG) neurons elicited robust ANO1-dependent depolarization. Furthermore, knockdown or deletion of ANO1 in DRG neurons substantially reduced nociceptive behavior in thermal pain models. These results indicate that ANO1 is a heat sensor that detects nociceptive thermal stimuli in sensory neurons and possibly mediates nociception.-
dc.language영어-
dc.language.isoen-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleThe calcium-activated chloride channel anoctamin 1 acts as a heat sensor in nociceptive neurons-
dc.typeArticle-
dc.contributor.affiliatedAuthorJang, Yong woo-
dc.identifier.doi10.1038/nn.3111-
dc.identifier.scopusid2-s2.0-84862896642-
dc.identifier.wosid000305819600020-
dc.identifier.bibliographicCitationNATURE NEUROSCIENCE, v.15, no.7, pp.1015 - 1021-
dc.relation.isPartOfNATURE NEUROSCIENCE-
dc.citation.titleNATURE NEUROSCIENCE-
dc.citation.volume15-
dc.citation.number7-
dc.citation.startPage1015-
dc.citation.endPage1021-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusCAPSAICIN-RECEPTOR-
dc.subject.keywordPlusNOXIOUS HEAT-
dc.subject.keywordPlusION CHANNELS-
dc.subject.keywordPlusPAIN PATHWAY-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusCURRENTS-
dc.subject.keywordPlusTMEM16A-
dc.subject.keywordPlusTRPV1-
dc.subject.keywordPlusRAT-
dc.identifier.urlhttps://www.nature.com/articles/nn.3111-
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