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Nanoelectrical characterization of individual exosomes secreted by A beta(42)-ingested cells using electrostatic force microscopy

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dc.contributor.authorChoi, Yeseong-
dc.contributor.authorKim, Su-Mi-
dc.contributor.authorHeo, Youhee-
dc.contributor.authorLee, Gyudo-
dc.contributor.authorKang, Ji Yoon-
dc.contributor.authorYoon, Dae Sung-
dc.date.accessioned2021-08-30T04:25:03Z-
dc.date.available2021-08-30T04:25:03Z-
dc.date.created2021-06-19-
dc.date.issued2021-01-08-
dc.identifier.issn0957-4484-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/50135-
dc.description.abstractQuantifying the physical properties of individual exosomes containing amyloid-beta(42)(A beta(42)) is crucial for a better understanding of an underpinning mechanism of Alzheimer's disease expression which is associated with the A beta(42)transfer. Because of the lack of proper tools, however, there have been very few studies on how the amount of A beta(42) affects the physical properties of exosomes. To answer the question, we investigated the physical properties of exosomes secreted by neuroblastoma by probing individual exosomes using electrostatic force microscopy. Interestingly, we observed that when the higher concentration of A beta(42) oligomers was fed to cells, the higher surface charge of the exosomes appeared. This result indicates that the exosomes contain more A beta(42) with the increase in A beta(42) concentration in cell media, implying that they serve as transport vesicles for A beta(42). Our approach could help to better understand how the neuronal exosomes are related to the propagation of neurodegenerative diseases and to seek how to make an early diagnosis of those diseases.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherIOP PUBLISHING LTD-
dc.subjectEXTRACELLULAR VESICLES-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectIDENTIFICATION-
dc.subjectPROPAGATION-
dc.subjectNANOPARTICLES-
dc.subjectBIOGENESIS-
dc.subjectTIP-
dc.titleNanoelectrical characterization of individual exosomes secreted by A beta(42)-ingested cells using electrostatic force microscopy-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Gyudo-
dc.contributor.affiliatedAuthorYoon, Dae Sung-
dc.identifier.doi10.1088/1361-6528/abba58-
dc.identifier.scopusid2-s2.0-85094222112-
dc.identifier.wosid000577199800001-
dc.identifier.bibliographicCitationNANOTECHNOLOGY, v.32, no.2-
dc.relation.isPartOfNANOTECHNOLOGY-
dc.citation.titleNANOTECHNOLOGY-
dc.citation.volume32-
dc.citation.number2-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusEXTRACELLULAR VESICLES-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusPROPAGATION-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusBIOGENESIS-
dc.subject.keywordPlusTIP-
dc.subject.keywordAuthorexosome-
dc.subject.keywordAuthoramyloid beta-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthoratomic force microscopy-
dc.subject.keywordAuthorelectrostatic force microscopy-
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