Cargando…
DDIT4 regulates mesenchymal stem cell fate by mediating between HIF1α and mTOR signalling
Stem cell fate decisions to remain quiescent, self-renew or differentiate are largely governed by the interplay between extracellular signals from the niche and the cell intrinsic signal cascades and transcriptional programs. Here we demonstrate that DNA Damage Inducible Transcript 4 (DDIT4) acts as...
Autores principales: | Gharibi, Borzo, Ghuman, Mandeep, Hughes, Francis J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120275/ https://www.ncbi.nlm.nih.gov/pubmed/27876894 http://dx.doi.org/10.1038/srep36889 |
Ejemplares similares
-
Akt- and Erk-mediated regulation of proliferation and differentiation during PDGFRβ-induced MSC self-renewal
por: Gharibi, Borzo, et al.
Publicado: (2012) -
The physiological mTOR complex 1 inhibitor DDIT4 mediates therapy resistance in glioblastoma
por: Foltyn, Martha, et al.
Publicado: (2019) -
PML nuclear bodies contribute to the basal expression of the mTOR inhibitor DDIT4
por: Salsman, Jayme, et al.
Publicado: (2017) -
Circulating levels of DDIT4 and mTOR, and contributions of BMI, inflammation and insulin sensitivity in hyperlipidemia
por: Pan, Xinyan, et al.
Publicado: (2022) -
p53-mediated AKT and mTOR inhibition requires RFX7 and DDIT4 and depends on nutrient abundance
por: Coronel, Luis, et al.
Publicado: (2021)