Hochschulschrift

Inactivation of Lsd1 triggers senescence in trophoblast stem cells by induction of Sirt4

Abstract: Coordination of energy metabolism is essential for homeostasis of stem cells, whereas an imbalance in energy homeostasis causes disease and accelerated aging. Here we show that deletion or enzymatic inactivation of lysine-specific demethylase 1 (Lsd1) triggers senescence in trophoblast stem cells (TSCs). Genome-wide transcriptional profiling of TSCs following Lsd1 inhibition shows gene set enrichment of aging and metabolic pathways. Consistently, global metabolomic and phenotypic analyses disclose an unbalanced redox status, decreased glutamine anaplerosis and mitochondrial function. Loss of homeostasis is caused by increased expression of sirtuin 4 (Sirt4), a Lsd1-repressed direct target gene. Accordingly, Sirt4 overexpression in wild-type TSCs recapitulates the senescence phenotype initiated by Lsd1 deletion or inhibition. Inversely, absence of Lsd1 enzymatic activity concomitant with knockdown of Sirt4 reestablishes normal glutamine anaplerosis, redox balance and mitochondrial function. In conclusion, by repression of Sirt4, Lsd1 directs the epigenetic control of TSC immortality via maintenance of metabolic flexibility

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Cell death & disease. - 8, 2 (2017) , e2631, ISSN: 2041-4889

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2019
Urheber
Castex Armendariz, Maria Josefina
Willmann, Dominica
Kanouni, Toufike
Arrigoni, Laura
Li, Yan
Friedrich, Marcel
Schleicher, Michael
Wöhrle, Simon
Pearson, Mark
Kraut, Norbert
Méret, Michaël
Manke, Thomas
Metzger, Eric
Schüle, Roland
Günther, Thomas

DOI
10.1038/cddis.2017.48
URN
urn:nbn:de:bsz:25-freidok-1404188
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
25.03.2025, 13:58 MEZ

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Objekttyp

  • Hochschulschrift

Beteiligte

Entstanden

  • 2019

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