Temporal and spatially controlled APP transgene expression using Cre-dependent alleles.
Ontology highlight
ABSTRACT: Although a large number of mouse models have been made to study Alzheimer's disease, only a handful allow experimental control over the location or timing of the protein being used to drive pathology. Other fields have used the Cre and the tamoxifen-inducible CreER driver lines to achieve precise spatial and temporal control over gene deletion and transgene expression, yet these tools have not been widely used in studies of neurodegeneration. Here, we describe two strategies for harnessing the wide range of Cre and CreER driver lines to control expression of disease-associated amyloid precursor protein (APP) in modeling Alzheimer's amyloid pathology. We show that CreER-based spatial and temporal control over APP expression can be achieved with existing lines by combining a Cre driver with
SUBMITTER: Koller EJ
PROVIDER: S-EPMC9118045 | biostudies-literature | 2022 May
REPOSITORIES: biostudies-literature
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