Dexamethasone regulates expression of BRUCE/Apollon and the proliferation of neural progenitor cells.
Glucocorticoid hormones (GHs) regulate cell proliferation of neural progenitor cells (NPCs) contributing to reduction of neurogenesis after stress. We show here that dexamethasone (Dex) decreases BRUCE/Apollon (BRUCE) in cultured NPCs in a GH-receptor-dependent manner. Downregulation of BRUCE by Dex or using silencing RNA reduced the number of proliferating NPCs, whilst ... overexpression of BRUCE counteracted the effect of Dex. Dex also elevated the deubiquitinating enzyme, Usp8/Ubpy, which via Nrdp1 decreases BRUCE. The results show that BRUCE is a target for GHs in the NPCs, and that BRUCE controls cell division of NPCs and possibly of other stem cells.
Mesh Terms:
Animals, Cell Proliferation, Dexamethasone, Down-Regulation, Embryo, Mammalian, Gene Expression Regulation, Neurogenesis, Neurons, Rats, Stem Cells, Ubiquitin-Conjugating Enzymes
Animals, Cell Proliferation, Dexamethasone, Down-Regulation, Embryo, Mammalian, Gene Expression Regulation, Neurogenesis, Neurons, Rats, Stem Cells, Ubiquitin-Conjugating Enzymes
FEBS Lett.
Date: Jul. 07, 2009
PubMed ID: 19527720
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