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CNS Neurosci Ther ; 27(2): 174-185, 2021 02.
Article in English | MEDLINE | ID: mdl-32961023

ABSTRACT

INTRODUCTION: Presenilin enhancer2 (Pen-2) is an essential subunit of γ-secretase, which is a key protease responsible for the cleavage of amyloid precursor protein (APP) and Notch. Mutations on Pen-2 cause familial Alzheimer disease (AD). However, it remains unknown whether Pen-2 regulates neuronal survival and neuroinflammation in the adult brain. METHODS: Forebrain neuron-specific Pen-2 conditional knockout (Pen-2 cKO) mice were generated for this study. Pen-2 cKO mice expressing Notch1 intracellular domain (NICD) conditionally in cortical neurons were also generated. RESULTS: Loss of Pen-2 causes astrogliosis followed by age-dependent cortical atrophy and neuronal loss. Loss of Pen-2 results in microgliosis and enhanced inflammatory responses in the cortex. Expression of NICD in Pen-2 cKO cortices ameliorates neither neurodegeneration nor neuroinflammation. CONCLUSIONS: Pen-2 is required for neuronal survival in the adult cerebral cortex. The Notch signaling may not be involved in neurodegeneration caused by loss of Pen-2.


Subject(s)
Aging/metabolism , Amyloid Precursor Protein Secretases/deficiency , Cerebral Cortex/metabolism , Gliosis/metabolism , Neurons/metabolism , Receptors, Notch/deficiency , Aging/genetics , Aging/pathology , Amyloid Precursor Protein Secretases/genetics , Animals , Atrophy , Cerebral Cortex/pathology , Disease Progression , Female , Gene Deletion , Gliosis/genetics , Gliosis/pathology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Mice, Transgenic , Neurons/pathology , Receptors, Notch/genetics
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