| Literature DB >> 26854229 |
Gabriela Martínez1, René L Vidal2, Pablo Mardones1, Felipe G Serrano3, Alvaro O Ardiles4, Craig Wirth5, Pamela Valdés1, Peter Thielen5, Bernard L Schneider6, Bredford Kerr7, Jose L Valdés8, Adrian G Palacios4, Nibaldo C Inestrosa3, Laurie H Glimcher9, Claudio Hetz10.
Abstract
Contextual memory formation relies on the induction of new genes in the hippocampus. A polymorphism in the promoter of the transcription factor XBP1 was identified as a risk factor for Alzheimer's disease and bipolar disorders. XBP1 is a major regulator of the unfolded protein response (UPR), mediating adaptation to endoplasmic reticulum (ER) stress. Using a phenotypic screen, we uncovered an unexpected function of XBP1 in cognition and behavior. Mice lacking XBP1 in the nervous system showed specific impairment of contextual memory formation and long-term potentiation (LTP), whereas neuronal XBP1s overexpression improved performance in memory tasks. Gene expression analysis revealed that XBP1 regulates a group of memory-related genes, highlighting brain-derived neurotrophic factor (BDNF), a key component in memory consolidation. Overexpression of BDNF in the hippocampus reversed the XBP1-deficient phenotype. Our study revealed an unanticipated function of XBP1 in cognitive processes that is apparently unrelated to its role in ER stress.Entities:
Mesh:
Substances:
Year: 2016 PMID: 26854229 DOI: 10.1016/j.celrep.2016.01.028
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423