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Secretory autophagy machinery and vesicular trafficking are involved in HMGB1 secretion

DC Field Value Language
dc.contributor.authorYoung Hun Kim-
dc.contributor.authorMan Sup Kwak-
dc.contributor.authorBin Lee-
dc.contributor.authorJae Min Shin-
dc.contributor.authorSowon Aum-
dc.contributor.authorIn Ho Park-
dc.contributor.authorMin Goo Lee-
dc.contributor.authorJeon-Soo Shin-
dc.date.accessioned2022-01-04T01:30:14Z-
dc.date.available2022-01-04T01:30:14Z-
dc.date.created2020-11-09-
dc.date.issued2021-09-
dc.identifier.issn1554-8627-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/10966-
dc.description.abstract© 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. Nuclear protein HMGB1 is secreted in response to various stimuli and functions as a danger-associated molecular pattern. Extracellular HMGB1 induces inflammation, cytokine production, and immune cell recruitment via activation of various receptors. As HMGB1 does not contain an endoplasmic reticulum-targeting signal peptide, HMGB1 is secreted via the endoplasmic reticulum-Golgi independently via an unconventional secretion pathway. However, the mechanism underlying HMGB1 secretion remains largely unknown. Here, we investigated the role of secretory autophagy machinery and vesicular trafficking in HMGB1 secretion. We observed that HSP90AA1 (heat shock protein 90 alpha family class A member 1), a stress-inducible protein, regulates the translocation of HMGB1 from the nucleus to the cytoplasm and its secretion through direct interaction. Additionally, geldanamycin, an HSP90AA1 inhibitor, reduced HMGB1 secretion. GORASP2/GRASP55 (golgi reassembly stacking protein 2), ARF1Q71L (ADP ribosylation factor 1), and SAR1AT39N (secretion associated Ras related GTPase 1A), which promoted unconventional protein secretion, increased HMGB1 secretion. HMGB1 secretion was inhibited by an early autophagy inhibitor and diminished in ATG5-deficient cells even when GORASP2 was overexpressed. In contrast, a late autophagy inhibitor increased HMGB1 secretion under the same conditions. The multivesicular body formation inhibitor GW4869 dramatically decreased HMGB1 secretion under HMGB1 secretion-inducing conditions. Thus, we demonstrated that secretory autophagy and multivesicular body formation mediate HMGB1 secretion.-
dc.language영어-
dc.publisherLandes Bioscience-
dc.titleSecretory autophagy machinery and vesicular trafficking are involved in HMGB1 secretion-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000575257200001-
dc.identifier.scopusid2-s2.0-85092076632-
dc.identifier.rimsid73300-
dc.contributor.affiliatedAuthorJeon-Soo Shin-
dc.identifier.doi10.1080/15548627.2020.1826690-
dc.identifier.bibliographicCitationAutophagy, v.17, no.9, pp.2345 - 2362-
dc.relation.isPartOfAutophagy-
dc.citation.titleAutophagy-
dc.citation.volume17-
dc.citation.number9-
dc.citation.startPage2345-
dc.citation.endPage2362-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusMOBILITY GROUP BOX-1-
dc.subject.keywordPlusUNCONVENTIONAL SECRETION-
dc.subject.keywordPlusCYTOPLASMIC TRANSLOCATION-
dc.subject.keywordPlusPROTEIN HMGB1-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusSTRESS-
dc.subject.keywordPlusREDOX-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusBIOGENESIS-
dc.subject.keywordAuthorautophagy-
dc.subject.keywordAuthorGORASP2-
dc.subject.keywordAuthorHMGB1-
dc.subject.keywordAuthorHSP90AA1-
dc.subject.keywordAuthorMVB formation-
dc.subject.keywordAuthorunconventional protein secretion-
Appears in Collections:
Center for Nanomedicine (나노의학 연구단) > 1. Journal Papers (저널논문)
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