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Stricker, S.H. ; Götz, M.

Epigenetic regulation of neural lineage elaboration: Implications for therapeutic reprogramming.

Neurobiol. Dis. 148:105174 (2021)
Verlagsversion DOI
Open Access Hybrid
Creative Commons Lizenzvertrag
The vulnerability of the mammalian brain is mainly due to its limited ability to generate new neurons once fully matured. Direct conversion of non-neuronal cells to neurons opens up a new avenue for therapeutic intervention and has made great strides also for in vivo applications in the injured brain. These great achievements raise the issue of adequate identity and chromatin hallmarks of the induced neurons. This may be particularly important, as aberrant epigenetic settings may reveal their adverse effects only in certain brain activity states. Therefore, we review here the knowledge about epigenetic memory and partially resetting of chromatin hallmarks from other reprogramming fields, before moving to the knowledge in direct neuronal reprogramming, which is still limited. Most importantly, novel tools are available now to manipulate specific epigenetic marks at specific sites of the genome. Applying these will eventually allow erasing aberrant epigenetic memory and paving the way towards new therapeutic approaches for brain repair.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Direct Reprogramming ; Epigenetics ; Neural Lineage; Pluripotent Stem-cells; Dna Methylation; Somatic-cells; Human Neurons; Brain Repair; Glial-cells; Muller Glia; Memory; Heterochromatin; Expression
Sprache englisch
Veröffentlichungsjahr 2021
Prepublished im Jahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 0969-9961
e-ISSN 1095-953X
Zeitschrift Neurobiology of Disease
Quellenangaben Band: 148, Heft: , Seiten: , Artikelnummer: 105174 Supplement: ,
Verlag Elsevier
Verlagsort 525 B St, Ste 1900, San Diego, Ca 92101-4495 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Stem Cell Research (ISF)
POF Topic(s) 30204 - Cell Programming and Repair
Forschungsfeld(er) Stem Cell and Neuroscience
PSP-Element(e) G-500800-001
Förderungen German Research Foundation
ERC
DOI 10.1016/j.nbd.2020.105174
WOS ID WOS:000607576400007
Scopus ID 85096701527
Erfassungsdatum 2020-12-03
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