Publication:
Proteome profiling of neuron-derived exosomes in alzheimer's disease reveals hemoglobin as a potential biomarker

dc.contributor.coauthorArıöz, Burak İbrahim
dc.contributor.coauthorTüfekçi, Kemal Uğur
dc.contributor.coauthorÖlçüm, Melis
dc.contributor.coauthorDurur, Devrim Yağmur
dc.contributor.coauthorBağrıyanık, H. Alper
dc.contributor.coauthorKeskinoğlu, Pembe
dc.contributor.coauthorYener, Görsev
dc.contributor.coauthorGenç, Şermin
dc.contributor.departmentDepartment of Molecular Biology and Genetics
dc.contributor.kuauthorAkarlar, Büşra
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.date.accessioned2024-11-09T23:04:11Z
dc.date.issued2021
dc.description.abstractAlzheimer's disease is a chronic and progressive neurodegenerative disorder, which is the most common cause of dementia worldwide. Although amyloid plaques and neurofibrillary tangles are identified as the hallmarks of the disease, the only valid diagnostic method yet is post-mortem imaging of these molecules in brain sections. Exosome is a type of extracellular vesicles secreted into extracellular space and plays fundamental roles in healthy and pathological conditions, including cell-to-cell communication. In this study, we aimed to investigate the proteomic contents of neuron-derived exosomes (NDEs) from AD patients and healthy controls (HCs) to identify a possible marker for AD diagnosis. We identified alpha-globin, beta-globin, and delta-globin increase in neuron-derived exosomes of AD patients compared to HCs with LC-MS/MS proteomics analysis. Then, we confirmed the high hemoglobin (Hb) level in NDEs of AD patients with ELISA. We found the area under the curve of hemoglobin level as 0.6913 with ROC analysis. Cargo proteins of NDEs may be useful diagnostic biomarker for AD.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK) [217S584] This study received financial support from the Scientific and Technological Research Council of Turkey (TUBITAK) (Project number 217S584).
dc.description.volume755
dc.identifier.doi10.1016/j.neulet.2021.135914
dc.identifier.eissn1872-7972
dc.identifier.issn0304-3940
dc.identifier.quartileQ3
dc.identifier.scopus2-s2.0-85105837092
dc.identifier.urihttps://doi.org/10.1016/j.neulet.2021.135914
dc.identifier.urihttps://hdl.handle.net/20.500.14288/8583
dc.identifier.wos647728900002
dc.keywordsExosome
dc.keywordsHemoglobin
dc.keywordsAlzheimer's disease oxidative stress
dc.keywordsPlasma exsomes
dc.keywordsDiagnosisI
dc.keywordsDementia
dc.keywordsProteins
dc.language.isoeng
dc.publisherElsevier Ireland Ltd
dc.relation.ispartofNeuroscience Letters
dc.subjectNeurosciences
dc.titleProteome profiling of neuron-derived exosomes in alzheimer's disease reveals hemoglobin as a potential biomarker
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorAkarlar, Büşra Aytül
local.contributor.kuauthorÖzlü, Nurhan
local.publication.orgunit1College of Sciences
local.publication.orgunit2Department of Molecular Biology and Genetics
relation.isOrgUnitOfPublicationaee2d329-aabe-4b58-ba67-09dbf8575547
relation.isOrgUnitOfPublication.latestForDiscoveryaee2d329-aabe-4b58-ba67-09dbf8575547
relation.isParentOrgUnitOfPublicationaf0395b0-7219-4165-a909-7016fa30932d
relation.isParentOrgUnitOfPublication.latestForDiscoveryaf0395b0-7219-4165-a909-7016fa30932d

Files