NeuroD2 Modulates Hippocampal Neuronal Organization and Axon Guidance During Aging

dc.contributor.authorBeker, Merve
dc.contributor.authorBolat, Busenur
dc.contributor.authorJohnson, Bahar Sarikamis
dc.contributor.authorErcin, Nilufer
dc.contributor.authorCakmak, Rabia Kalkan
dc.contributor.authorKaya, Sare B.
dc.contributor.authorBesli, Nail
dc.date.accessioned2025-11-16T19:34:36Z
dc.date.issued2025
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground/Aim: Biological aging refers to the progressive deterioration of an organism's functions due to accumulated cellular and molecular damage. NeuroD2, a critical transcription factor, plays a crucial role in neuronal development and synaptic maturation. This study investigates the role of NeuroD2 in hippocampal neuron organization, focusing on hilar mossy cells during aging, and employs bioinformatics to identify NeuroD2 targets linked to cellular aging. Materials and Methods: We used 21 adult C57Bl/6 mice, categorized into three age groups: young (2 months), old (12 months), and very old (24 months). Mice were administered BrdU intraperitoneally for three consecutive days, 10 days before euthanasia. The brains were harvested and analyzed using immunofluorescence, Western blotting, and quantitative real-time PCR to evaluate NeuroD2 expression and associated signaling pathways in hippocampal tissue. Additionally, bioinformatics analysis was performed using two open-access datasets (ProteomeXchange Consortium, Dataset identifier: PXD043352; Gene Expression Omnibus, GEO: GSE67539) and to explore potential interactions between NeuroD2 targets and biological aging components. Results: Our results revealed that NeuroD2 expression changed significantly with age and correlated with AKT signaling. Moreover, we identified a potential link between NeuroD2 activity and the AKT pathway, indicating NeuroD2's role in mitigating aging-related stress. Bioinformatics analysis identified 513 down-regulated and 638 up- regulated proteins, with NeuroD2 targets involved in axonal projection showing increased expression in older mice. Contrary to expectations, pathway enrichment analysis highlighted axon guidance molecules rather than oxidative stress markers. Conclusion: This study underscores NeuroD2's critical role in preserving hippocampal integrity and reveals molecular mechanisms underlying age-related neuronal changes. Our findings provide insights into the role of NeuroD2 in regulating key pathways during healthy aging, potentially mitigating the impacts of aging.
dc.identifier.doi10.21873/invivo.14000
dc.identifier.endpage2065
dc.identifier.issn0258-851X
dc.identifier.issn1791-7549
dc.identifier.issue4
dc.identifier.pmid40579006
dc.identifier.scopus2-s2.0-105010011958
dc.identifier.scopusqualityQ2
dc.identifier.startpage2050
dc.identifier.urihttps://doi.org/10.21873/invivo.14000
dc.identifier.urihttps://hdl.handle.net/20.500.14730/15399
dc.identifier.volume39
dc.identifier.wosWOS:001522192700016
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherInt Inst Anticancer Research
dc.relation.ispartofIn Vivo
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectAging
dc.subjectAKT
dc.subjectcell signaling
dc.subjecthippocampus
dc.subjectNeuroD2.
dc.titleNeuroD2 Modulates Hippocampal Neuronal Organization and Axon Guidance During Aging
dc.typeArticle

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