000169366 001__ 169366 000169366 005__ 20231120155332.0 000169366 0247_ $$2doi$$a10.1002/hipo.23494 000169366 0247_ $$2pmid$$apmid:36624660 000169366 0247_ $$2ISSN$$a1050-9631 000169366 0247_ $$2ISSN$$a1098-1063 000169366 0247_ $$2altmetric$$aaltmetric:141036757 000169366 037__ $$aDZNE-2023-00141 000169366 041__ $$aEnglish 000169366 082__ $$a610 000169366 1001_ $$0P:(DE-2719)2810548$$aZocher, Sara$$b0$$eFirst author$$udzne 000169366 245__ $$aEpigenetic aging in adult neurogenesis. 000169366 260__ $$aNew York, NY [u.a.]$$bWiley$$c2023 000169366 3367_ $$2DRIVER$$aarticle 000169366 3367_ $$2DataCite$$aOutput Types/Journal article 000169366 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1680532540_25881$$xReview Article 000169366 3367_ $$2BibTeX$$aARTICLE 000169366 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000169366 3367_ $$00$$2EndNote$$aJournal Article 000169366 500__ $$aFunding information: Deutsche Forschungsgemeinschaft, Grant/Award Numbers: TO1347/4-1, TO1347/3-1; H2020 European Research Council, Grant/Award Numbers: EAGER, 804468 000169366 520__ $$aNeural stem cells (NSCs) in the hippocampus generate new neurons throughout life, which functionally contribute to cognitive flexibility and mood regulation. Yet adult hippocampal neurogenesis substantially declines with age and age-related impairments in NSC activity underlie this reduction. Particularly, increased NSC quiescence and consequently reduced NSC proliferation are considered to be major drivers of the low neurogenesis levels in the aged brain. Epigenetic regulators control the gene expression programs underlying NSC quiescence, proliferation and differentiation and are hence critical to the regulation of adult neurogenesis. Epigenetic alterations have also emerged as central hallmarks of aging, and recent studies suggest the deterioration of the NSC-specific epigenetic landscape as a driver of the age-dependent decline in adult neurogenesis. In this review, we summarize the recently accumulating evidence for a role of epigenetic dysregulation in NSC aging and propose perspectives for future research directions. 000169366 536__ $$0G:(DE-HGF)POF4-352$$a352 - Disease Mechanisms (POF4-352)$$cPOF4-352$$fPOF IV$$x0 000169366 588__ $$aDataset connected to CrossRef, PubMed, , Journals: pub.dzne.de 000169366 650_7 $$2Other$$aDNA methylation 000169366 650_7 $$2Other$$aLamin B1 000169366 650_7 $$2Other$$aaging 000169366 650_7 $$2Other$$achromatin 000169366 650_7 $$2Other$$aepigenetic 000169366 650_7 $$2Other$$ahippocampus 000169366 650_7 $$2Other$$ahistone 000169366 650_7 $$2Other$$aneural stem cells 000169366 650_7 $$2Other$$aneurogenesis 000169366 650_2 $$2MeSH$$aNeurogenesis: physiology 000169366 650_2 $$2MeSH$$aCell Differentiation: genetics 000169366 650_2 $$2MeSH$$aNeurons: metabolism 000169366 650_2 $$2MeSH$$aHippocampus: physiology 000169366 650_2 $$2MeSH$$aEpigenesis, Genetic 000169366 7001_ $$0P:(DE-2719)2814117$$aToda, Tomohisa$$b1$$eLast author$$udzne 000169366 770__ $$aAdult Neurogenesis in the Hippocampus 000169366 773__ $$0PERI:(DE-600)1498049-6$$a10.1002/hipo.23494$$gp. hipo.23494$$n4$$p347-359$$tHippocampus$$v33$$x1050-9631$$y2023 000169366 8564_ $$uhttps://pub.dzne.de/record/169366/files/DZNE-2023-00141.pdf$$yOpenAccess 000169366 8564_ $$uhttps://pub.dzne.de/record/169366/files/DZNE-2023-00141.pdf?subformat=pdfa$$xpdfa$$yOpenAccess 000169366 909CO $$ooai:pub.dzne.de:169366$$pdnbdelivery$$pdriver$$pVDB$$popen_access$$popenaire 000169366 9101_ $$0I:(DE-588)1065079516$$6P:(DE-2719)2810548$$aDeutsches Zentrum für Neurodegenerative Erkrankungen$$b0$$kDZNE 000169366 9101_ $$0I:(DE-588)1065079516$$6P:(DE-2719)2814117$$aDeutsches Zentrum für Neurodegenerative Erkrankungen$$b1$$kDZNE 000169366 9131_ $$0G:(DE-HGF)POF4-352$$1G:(DE-HGF)POF4-350$$2G:(DE-HGF)POF4-300$$3G:(DE-HGF)POF4$$4G:(DE-HGF)POF$$aDE-HGF$$bGesundheit$$lNeurodegenerative Diseases$$vDisease Mechanisms$$x0 000169366 9141_ $$y2023 000169366 915__ $$0StatID:(DE-HGF)0160$$2StatID$$aDBCoverage$$bEssential Science Indicators$$d2022-11-22 000169366 915__ $$0StatID:(DE-HGF)1190$$2StatID$$aDBCoverage$$bBiological Abstracts$$d2022-11-22 000169366 915__ $$0StatID:(DE-HGF)3001$$2StatID$$aDEAL Wiley$$d2022-11-22$$wger 000169366 915__ $$0StatID:(DE-HGF)0113$$2StatID$$aWoS$$bScience Citation Index Expanded$$d2022-11-22 000169366 915__ $$0StatID:(DE-HGF)0510$$2StatID$$aOpenAccess 000169366 915__ $$0LIC:(DE-HGF)CCBY4$$2HGFVOC$$aCreative Commons Attribution CC BY 4.0 000169366 915__ $$0StatID:(DE-HGF)0420$$2StatID$$aNationallizenz$$d2023-10-21$$wger 000169366 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bClarivate Analytics Master Journal List$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)1050$$2StatID$$aDBCoverage$$bBIOSIS Previews$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)1030$$2StatID$$aDBCoverage$$bCurrent Contents - Life Sciences$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)0100$$2StatID$$aJCR$$bHIPPOCAMPUS : 2022$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)0600$$2StatID$$aDBCoverage$$bEbsco Academic Search$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)0030$$2StatID$$aPeer Review$$bASC$$d2023-10-21 000169366 915__ $$0StatID:(DE-HGF)9900$$2StatID$$aIF < 5$$d2023-10-21 000169366 9201_ $$0I:(DE-2719)1710014$$kAG Toda$$lNuclear Architecture in Neural Plasticity and Aging$$x0 000169366 980__ $$ajournal 000169366 980__ $$aVDB 000169366 980__ $$aI:(DE-2719)1710014 000169366 980__ $$aUNRESTRICTED 000169366 9801_ $$aFullTexts