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Mitochondria-derived peptide SHLP2 regulates energy homeostasis through the activation of hypothalamic neurons.

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dc.contributor.authorKim, Seul Ki-
dc.contributor.authorTran, Le Trung-
dc.contributor.authorNamKoong, Cherl-
dc.contributor.authorChoi, Hyung Jin-
dc.contributor.authorChun, Hye Jin-
dc.contributor.authorLee, Yong-Ho-
dc.contributor.authorCheon, MyungHyun-
dc.contributor.authorChung, ChiHye-
dc.contributor.authorHwang, Junmo-
dc.contributor.authorLim, Hyun-Ho-
dc.contributor.authorShin, Dong Min-
dc.contributor.authorChoi, Yun-Hee-
dc.contributor.authorKim, Ki Woo-
dc.date.accessioned2023-08-16T09:28:47Z-
dc.date.available2023-08-16T09:28:47Z-
dc.date.issued2023-08-
dc.identifier.issn2041-1723-
dc.identifier.issn2041-1723-
dc.identifier.urihttp://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/112-
dc.description.abstractSmall humanin-like peptide 2 (SHLP2) is a mitochondrial-derived peptide implicated in several biological processes such as aging and oxidative stress. However, its functional role in the regulation of energy homeostasis remains unclear, and its corresponding receptor is not identified. Hereby, we demonstrate that both systemic and intracerebroventricular (ICV) administrations of SHLP2 protected the male mice from high-fat diet (HFD)-induced obesity and improved insulin sensitivity. In addition, the activation of pro-opiomelanocortin (POMC) neurons by SHLP2 in the arcuate nucleus of the hypothalamus (ARC) is involved in the suppression of food intake and the promotion of thermogenesis. Through high-throughput structural complementation screening, we discovered that SHLP2 binds to and activates chemokine receptor 7 (CXCR7). Taken together, our study not only reveals the therapeutic potential of SHLP2 in metabolic disorders but also provides important mechanistic insights into how it exerts its effects on energy homeostasis. © 2023. The Author(s).-
dc.language영어-
dc.language.isoENG-
dc.publisherNature Publishing Group-
dc.titleMitochondria-derived peptide SHLP2 regulates energy homeostasis through the activation of hypothalamic neurons.-
dc.typeArticle-
dc.publisher.locationUnited Kingdom-
dc.identifier.doi10.1038/s41467-023-40082-7-
dc.identifier.scopusid2-s2.0-85165272958-
dc.identifier.wosid001037980500020-
dc.identifier.bibliographicCitationNature Communications, v.14, no.1, pp 4321-
dc.citation.titleNature Communications-
dc.citation.volume14-
dc.citation.number1-
dc.citation.startPage4321-
dc.type.docTypeJournal Article;Research Support, Non-U.S. Gov't-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusBETA-ARRESTIN-
dc.subject.keywordPlusOBESITY-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusHUMANIN-
dc.subject.keywordPlusLEPTIN-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusERK1/2-
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연구본부 (신경·혈관단위체 연구그룹)
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