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  Cellular senescence promotes progenitor cell expansion during axolotl limb regeneration.

Yu, Q., Walters, H. E., Pasquini, G., Singh, S. P., Lachnit, M., Oliveira, C., et al. (2023). Cellular senescence promotes progenitor cell expansion during axolotl limb regeneration. Developmental cell, 58(22), 2416-2427. doi:10.1016/j.devcel.2023.09.009.

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Yu, Qinghao, Autor
Walters, Hannah E, Autor
Pasquini, Giovanni, Autor
Singh, Sumeet Pal, Autor
Lachnit, Martina1, Autor           
Oliveira, Catarina1, Autor           
León-Periñán, Daniel, Autor
Petzold, Andreas, Autor
Kesavan, Preethi, Autor
Adrados, Cristina Subiran, Autor
Garteizgogeascoa, Ines, Autor
Knapp, Dunja1, Autor           
Wagner, Anne, Autor
Bernardos, Andrea, Autor
Alfonso, María, Autor
Nadar, Gayathri, Autor
Graf, Alwin M, Autor
Troyanovskiy, Konstantin E, Autor
Dahl, Andreas, Autor
Busskamp, Volker, Autor
Martínez-Máñez, Ramón, AutorYun, Maximina H1, Autor            mehr..
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Zusammenfassung: Axolotl limb regeneration is accompanied by the transient induction of cellular senescence within the blastema, the structure that nucleates regeneration. The precise role of this blastemal senescent cell (bSC) population, however, remains unknown. Here, through a combination of gain- and loss-of-function assays, we elucidate the functions and molecular features of cellular senescence in vivo. We demonstrate that cellular senescence plays a positive role during axolotl regeneration by creating a pro-proliferative niche that supports progenitor cell expansion and blastema outgrowth. Senescent cells impact their microenvironment via Wnt pathway modulation. Further, we identify a link between Wnt signaling and senescence induction and propose that bSC-derived Wnt signals facilitate the proliferation of neighboring cells in part by preventing their induction into senescence. This work defines the roles of cellular senescence in the regeneration of complex structures.

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 Datum: 2023-11-20
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1016/j.devcel.2023.09.009
Anderer: cbg-8636
PMID: 37879337
 Art des Abschluß: -

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Titel: Developmental cell
  Andere : Dev Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 58 (22) Artikelnummer: - Start- / Endseite: 2416 - 2427 Identifikator: -