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dc.contributor.author Kang, Chan Woo -
dc.contributor.author Han, Ye Eon -
dc.contributor.author Lee, Mi Kyung -
dc.contributor.author Cho, Yoon Hee -
dc.contributor.author Kang, Na Na -
dc.contributor.author Koo, Jae Hyung -
dc.contributor.author Ku, Cheol Ryong -
dc.contributor.author Lee, Eun Jig -
dc.date.accessioned 2018-05-02T00:12:52Z -
dc.date.available 2018-05-02T00:12:52Z -
dc.date.created 2018-04-30 -
dc.date.issued 2018-04 -
dc.identifier.issn 1226-3613 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/6249 -
dc.description.abstract Olfactory marker protein (OMP) is a marker of olfactory receptor-mediated chemoreception, even outside the olfactory system. Here, we report that OMP expression in the pituitary gland plays a role in basal and thyrotropin-releasing hormone (TRH)-induced prolactin (PRL) production and secretion. We found that OMP was expressed in human and rodent pituitary glands, especially in PRL-secreting lactotrophs. OMP knockdown in GH4 rat pituitary cells increased PRL production and secretion via extracellular signal-regulated kinase (ERK)1/2 signaling. Real-time PCR analysis and the Ca2+ influx assay revealed that OMP was critical for TRH-induced PRL secretion. OMP-knockout mice showed lower fertility than control mice, which was associated with increased basal PRL production via activation of ERK1/2 signaling and reduced TRH-induced PRL secretion. However, both in vitro and in vivo results indicated that OMP was only required for hormone production and secretion because ERK1/2 activation failed to stimulate cell proliferation. Additionally, patients with prolactinoma lacked OMP expression in tumor tissues with hyperactivated ERK1/2 signaling. These findings indicate that OMP plays a role in PRL production and secretion in lactotrophs through the modulation of Ca2+ and TRH signaling. © 2018 The Author(s). -
dc.language English -
dc.publisher Nature Publishing Group -
dc.title Olfactory marker protein regulates prolactin secretion and production by modulating Ca2+ and TRH signaling in lactotrophs -
dc.type Article -
dc.identifier.doi 10.1038/s12276-018-0035-z -
dc.identifier.scopusid 2-s2.0-85045096918 -
dc.identifier.bibliographicCitation Experimental and Molecular Medicine, v.50, no.4, pp.1 - 11 -
dc.identifier.kciid ART002342553 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus THYROTROPIN-RELEASING-HORMONE -
dc.subject.keywordPlus VECTOR-MEDIATED RESCUE -
dc.subject.keywordPlus PITUITARY-CELLS -
dc.subject.keywordPlus GENE-EXPRESSION -
dc.subject.keywordPlus NEUROENDOCRINE CARCINOMAS -
dc.subject.keywordPlus ADENYLYL-CYCLASE -
dc.subject.keywordPlus RECEPTOR -
dc.subject.keywordPlus MOUSE -
dc.subject.keywordPlus OMP -
dc.subject.keywordPlus KINASE -
dc.citation.endPage 11 -
dc.citation.number 4 -
dc.citation.startPage 1 -
dc.citation.title Experimental and Molecular Medicine -
dc.citation.volume 50 -
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Department of New Biology Brain-Immune Axis Laboratory 1. Journal Articles

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