| Literature DB >> 30692248 |
Jina Park1, Francesco Longo2, Seung Ju Park1, Seulgi Lee1, Mihyun Bae3, Richa Tyagi4, Jin-Hee Han1, Seyun Kim5,6, Emanuela Santini7, Eric Klann8, Solomon H Snyder9,10,11.
Abstract
Inositol polyphosphate multikinase (IPMK), the key enzyme for the biosynthesis of higher inositol polyphosphates and phosphatidylinositol 3,4,5-trisphosphate, also acts as a versatile signaling player in regulating tissue growth and metabolism. To elucidate neurobehavioral functions of IPMK, we generated mice in which IPMK was deleted from the excitatory neurons of the postnatal forebrain. These mice showed no deficits in either novel object recognition or spatial memory. IPMK conditional knockout mice formed cued fear memory normally but displayed enhanced fear extinction. Signaling analyses revealed dysregulated expression of neural genes accompanied by selective activation of the mechanistic target of rapamycin (mTOR) regulatory enzyme p85 S6 kinase 1 (S6K1) in the amygdala following fear extinction. The IPMK mutants also manifested facilitated hippocampal long-term potentiation. These findings establish a signaling action of IPMK that mediates fear extinction.Entities:
Keywords: fear extinction; inositol polyphosphate multikinase; long-term potentiation; memory
Mesh:
Substances:
Year: 2019 PMID: 30692248 PMCID: PMC6377498 DOI: 10.1073/pnas.1812771116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205