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Brain-specific chemokine FAM19A5 induces hypothalamic inflammation

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dc.contributor.authorKang, Dasol-
dc.contributor.authorKim, Han Rae-
dc.contributor.authorKim, Kwang Kon-
dc.contributor.authorKim, Dong Hee-
dc.contributor.authorJeong, Bora-
dc.contributor.authorJin, Sungho-
dc.contributor.authorPark, Jeong Woo-
dc.contributor.authorSeong, Jae Young-
dc.contributor.authorLee, Byung Ju-
dc.date.accessioned2021-08-31T06:22:01Z-
dc.date.available2021-08-31T06:22:01Z-
dc.date.created2021-06-18-
dc.date.issued2020-03-19-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/57247-
dc.description.abstractThe cytokine-like protein FAM19A5 is highly expressed in the brain, but little is known about its functions there. Here, we found that FAM19A5 was expressed in mouse hypothalamic cells expressing proopiomelanocortin (POMC) and neuropeptide Y (NPY)/agouti-related peptide (AgRP), and in the microglia. Tumor necrosis factor-alpha (TNF-alpha), which induces inflammatory sickness responses, greatly increased hypothalamic expression of FAM19A5. Knockdown of FAM19A5 expression resulted in decreased TNF-alpha-induced anorexia, body weight loss and TNF-alpha-induced expression of inflammatory factors. In contrast, intracerebroventricular administration of FAM19A5 induced anorexia, body weight loss and hyperthermia, together with increased expression of inflammatory factors. FAM19A5 injection also induced increases in c-fos activation and POMC mRNA level in hypothalamic POMC neurons. Together, these results suggest that FAM19A5 plays an important role in hypothalamic inflammatory responses. (C) 2020 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectPROOPIOMELANOCORTIN NEURONS-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectSICKNESS BEHAVIOR-
dc.subjectPROSTAGLANDINS-
dc.subjectEXPRESSION-
dc.subjectNUCLEUS-
dc.subjectFAMILY-
dc.titleBrain-specific chemokine FAM19A5 induces hypothalamic inflammation-
dc.typeArticle-
dc.contributor.affiliatedAuthorSeong, Jae Young-
dc.identifier.doi10.1016/j.bbrc.2019.12.119-
dc.identifier.scopusid2-s2.0-85077932218-
dc.identifier.wosid000526787700002-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.523, no.4, pp.829 - 834-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume523-
dc.citation.number4-
dc.citation.startPage829-
dc.citation.endPage834-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusPROOPIOMELANOCORTIN NEURONS-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusSICKNESS BEHAVIOR-
dc.subject.keywordPlusPROSTAGLANDINS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusNUCLEUS-
dc.subject.keywordPlusFAMILY-
dc.subject.keywordAuthorTumor necrosis factor-alpha (TNF-alpha)-
dc.subject.keywordAuthorHypothalamic inflammation-
dc.subject.keywordAuthorSickness responses-
dc.subject.keywordAuthorAnorexia-
dc.subject.keywordAuthorHyperthermia-
dc.subject.keywordAuthorProinflammatory cytokines-
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