The ubiquitin ligase UBE4B regulates amyloid precursor protein ubiquitination, endosomal trafficking, and amyloid β42 generation and secretion

Mol Cell Neurosci. 2020 Oct:108:103542. doi: 10.1016/j.mcn.2020.103542. Epub 2020 Aug 22.

Abstract

The extracellular accumulation of amyloid β (Aβ) fragments of amyloid precursor protein (APP) in brain parenchyma is a pathological hallmark of Alzheimer's disease (AD). APP can be cleaved into Aβ on late endosomes/multivesicular bodies (MVBs). E3 ubiquitin ligases have been linked to Aβ production, but specific E3 ligases associated with APP ubiquitination that may affect targeting of APP to endosomes have not yet been described. Using cultured cortical neurons isolated from rat pups, we reconstituted APP movement into the internal vesicles (ILVs) of MVBs. Loss of endosomal sorting complexes required for transport (ESCRT) components inhibited APP movement into ILVs and increased endosomal Aβ42 generation, implying a requirement for APP ubiquitination. We identified an ESCRT-binding and APP-interacting endosomal E3 ubiquitin ligase, ubiquitination factor E4B (UBE4B) that regulates APP ubiquitination. Depleting UBE4B in neurons inhibited APP ubiquitination and internalization into MVBs, resulting in increased endosomal Aβ42 levels and increased neuronal secretion of Aβ42. When we examined AD brains, we found levels of the UBE4B-interacting ESCRT component, hepatocyte growth factor-regulated tyrosine kinase substrate (Hrs), were significantly decreased in AD brains. These data suggest that ESCRT components critical for membrane protein sorting in the endocytic pathway are altered in AD. These results indicate that the molecular machinery underlying endosomal trafficking of APP, including the ubiquitin ligase UBE4B, regulates Aβ levels and may play an essential role in AD progression.

Keywords: Alzheimer's disease (AD); Amyloid β (Aβ); Endocytosis; Membrane trafficking; Multivesicular body (MVB); Ubiquitination factor E4B (UBE4B).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Peptides / metabolism*
  • Animals
  • Cells, Cultured
  • Endosomal Sorting Complexes Required for Transport / metabolism
  • Endosomes / metabolism*
  • Female
  • HEK293 Cells
  • Humans
  • Male
  • Neurons / metabolism*
  • Peptide Fragments / metabolism*
  • Protein Transport
  • Rats
  • Secretory Vesicles / metabolism
  • Ubiquitination*

Substances

  • Amyloid beta-Peptides
  • Endosomal Sorting Complexes Required for Transport
  • Peptide Fragments
  • amyloid beta-protein (1-42)