CD33 modulates TREM2: convergence of Alzheimer loci

Nat Neurosci. 2015 Nov;18(11):1556-8. doi: 10.1038/nn.4126. Epub 2015 Sep 28.

Abstract

We used a protein quantitative trait analysis in monocytes from 226 individuals to evaluate cross-talk between Alzheimer loci. The NME8 locus influenced PTK2B and the CD33 risk allele led to greater TREM2 expression. There was also a decreased TREM1/TREM2 ratio with a TREM1 risk allele, decreased TREM2 expression with CD33 suppression and elevated cortical TREM2 mRNA expression with amyloid pathology.

Publication types

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

MeSH terms

  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism*
  • Amyloid / metabolism
  • Genetic Predisposition to Disease*
  • Humans
  • Membrane Glycoproteins / genetics*
  • Membrane Glycoproteins / metabolism*
  • Microglia / metabolism
  • Mutation / genetics*
  • Receptors, Immunologic / biosynthesis
  • Receptors, Immunologic / genetics*
  • Receptors, Immunologic / metabolism*
  • Sialic Acid Binding Ig-like Lectin 3 / metabolism*

Substances

  • Amyloid
  • CD33 protein, human
  • Membrane Glycoproteins
  • Receptors, Immunologic
  • Sialic Acid Binding Ig-like Lectin 3
  • TREM2 protein, human