IL-10 alters immunoproteostasis in APP mice, increasing plaque burden and worsening cognitive behavior

Neuron. 2015 Feb 4;85(3):519-33. doi: 10.1016/j.neuron.2014.11.020. Epub 2015 Jan 22.

Abstract

Anti-inflammatory strategies are proposed to have beneficial effects in Alzheimer's disease. To explore how anti-inflammatory cytokine signaling affects Aβ pathology, we investigated the effects of adeno-associated virus (AAV2/1)-mediated expression of Interleukin (IL)-10 in the brains of APP transgenic mouse models. IL-10 expression resulted in increased Aβ accumulation and impaired memory in APP mice. A focused transcriptome analysis revealed changes consistent with enhanced IL-10 signaling and increased ApoE expression in IL-10-expressing APP mice. ApoE protein was selectively increased in the plaque-associated insoluble cellular fraction, likely because of direct interaction with aggregated Aβ in the IL-10-expressing APP mice. Ex vivo studies also show that IL-10 and ApoE can individually impair glial Aβ phagocytosis. Our observations that IL-10 has an unexpected negative effect on Aβ proteostasis and cognition in APP mouse models demonstrate the complex interplay between innate immunity and proteostasis in neurodegenerative diseases, an interaction we call immunoproteostasis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amyloid beta-Protein Precursor* / genetics
  • Animals
  • Animals, Newborn
  • Cells, Cultured
  • Cognition Disorders / immunology
  • Cognition Disorders / metabolism*
  • HEK293 Cells
  • Humans
  • Immunoproteins / biosynthesis*
  • Interleukin-10 / biosynthesis*
  • Mice
  • Mice, Transgenic
  • Plaque, Amyloid / immunology
  • Plaque, Amyloid / metabolism*
  • Proteostasis Deficiencies / immunology
  • Proteostasis Deficiencies / metabolism*

Substances

  • Amyloid beta-Protein Precursor
  • IL10 protein, mouse
  • Immunoproteins
  • Interleukin-10