Fbxo2 Regulates APP Levels and Processing

نویسندگان

  • Graham Atkin
  • Jack Hunt
  • Eiko Minakawa
  • Lisa Sharkey
  • Nathan Tipper
  • William Tennant
  • Henry L. Paulson
چکیده

The Amyloid Precursor Protein (APP) is an integral membrane glycoprotein whose cleavage products, particularly Amyloid-β, accumulate in Alzheimer’s Disease (AD). APP is present at synapses and is thought to play a role in both the formation and plasticity of these critical neuronal structures. Despite the central role suggested for APP in AD pathogenesis, the mechanisms regulating APP in neurons and its processing into cleavage products remain incompletely understood. Fbox only protein 2 (Fbxo2), a neuron-enriched ubiquitin ligase substrate adaptor that preferentially binds high-mannose glycans on glycoproteins, was previously implicated in APP processing by facilitating the degradation of the APP-cleaving beta-secretase, BACE1. Here we sought to determine whether Fbxo2 plays a similar role for other glycoproteins in the amyloid processing pathway. We present in vitro and in vivo evidence that APP is itself a substrate for Fbxo2. APP levels were decreased in the presence of Fbxo2 in non-neuronal cells, and increased in both cultured hippocampal neurons and brain tissue from Fbxo2 knockout mice. The processing of APP into its cleavage products was also increased in hippocampi and cultured hippocampal neurons lacking Fbxo2. In hippocampal slices, this increase in cleavage products was accompanied by a significant reduction in APP at the cell surface. Taken together, these results suggest that Fbxo2 regulates APP levels and processing in the brain and may play a role in modulating AD

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تاریخ انتشار 2014