Phosphoproteomics identifies microglial Siglec-F inflammatory response during neurodegeneration

Mol Syst Biol. 2020 Dec;16(12):e9819. doi: 10.15252/msb.20209819.

Abstract

Alzheimer's disease (AD) is characterized by the appearance of amyloid-β plaques, neurofibrillary tangles, and inflammation in brain regions involved in memory. Using mass spectrometry, we have quantified the phosphoproteome of the CK-p25, 5XFAD, and Tau P301S mouse models of neurodegeneration. We identified a shared response involving Siglec-F which was upregulated on a subset of reactive microglia. The human paralog Siglec-8 was also upregulated on microglia in AD. Siglec-F and Siglec-8 were upregulated following microglial activation with interferon gamma (IFNγ) in BV-2 cell line and human stem cell-derived microglia models. Siglec-F overexpression activates an endocytic and pyroptotic inflammatory response in BV-2 cells, dependent on its sialic acid substrates and immunoreceptor tyrosine-based inhibition motif (ITIM) phosphorylation sites. Related human Siglecs induced a similar response in BV-2 cells. Collectively, our results point to an important role for mouse Siglec-F and human Siglec-8 in regulating microglial activation during neurodegeneration.

Keywords: Alzheimer's disease; Siglec-8; Siglec-F; microglia; phosphoproteomics.

Publication types

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

MeSH terms

  • Alzheimer Disease / metabolism
  • Alzheimer Disease / pathology
  • Amino Acid Sequence
  • Animals
  • Antibodies / metabolism
  • Cell Death
  • Cell Line
  • Humans
  • Inflammation / metabolism
  • Inflammation / pathology*
  • Interferon-gamma / metabolism
  • Mice, Transgenic
  • Microglia / metabolism*
  • Microglia / pathology
  • Nerve Degeneration / metabolism
  • Nerve Degeneration / pathology*
  • Peptides / metabolism
  • Phagocytosis
  • Phosphoproteins / metabolism*
  • Phosphotyrosine / metabolism
  • Proteome / metabolism
  • Proteomics*
  • Sialic Acid Binding Immunoglobulin-like Lectins / chemistry
  • Sialic Acid Binding Immunoglobulin-like Lectins / metabolism*
  • Signal Transduction
  • Up-Regulation

Substances

  • Antibodies
  • Peptides
  • Phosphoproteins
  • Proteome
  • Sialic Acid Binding Immunoglobulin-like Lectins
  • Siglecf protein, mouse
  • Phosphotyrosine
  • Interferon-gamma