Opposing effects of membrane-anchored CX3CL1 on amyloid and tau pathologies via the p38 MAPK pathway

Sungho Lee, Guixiang Xu, Taylor R. Jay, Richard M. Ransohoff, Bruce Lamb, Sabina Bhatta, Bruce T. Lamb, Gary E. Landreth, Bruce T. Lamb, Taylor R. Jay, Sungho Lee, Ki Wook Kim, Steffen Jung

Research output: Contribution to journalArticle

47 Citations (Scopus)

Abstract

Several Alzheimer's disease (AD) risk genes are specifically expressed by microglia within the CNS. However, the mechanisms by which microglia regulate the pathological hallmarks of AD—extracellular deposition of β-amyloid (Aβ) and intraneuronal hyperphosphorylation of microtubule-associated protein tau (MAPT)—remain to be established. Notably, deficiency for the microglial CX3CR1 receptor has opposing effects on Aβ and MAPT pathologies. CX3CL1, the neuronally derived cognate ligand for CX3CR1, signals both in membrane-anchored and soluble forms. In this study, we sought to determine the relative contribution on membrane-anchored versus soluble CX3CL1 in regulating the microglia-mediated amelioration of Aβ pathology, as well as provide insight into the potential downstream microglial-based mechanisms. As expected, CX3CL1 deficiency reduced Aβ deposition in APPPS1 animals in a similar manner to CX3CR1 deficiency. Surprisingly, however, CX3CL1-deficient APPPS1 animals exhibited enhanced neuronal MAPT phosphorylation despite reduced amyloid burden. Importantly, neither of these phenotypes was altered by transgenic expression of the soluble CX3CL1 isoform, suggesting that it is the membrane-anchored version of CX3CL1 that regulates microglial phagocytosis of Aβ and neuronal MAPT phosphorylation. Analysis of transcript levels in purified microglia isolated from APPPS1 mice with the various CX3CL1/CX3CR1 genotypes revealed increased expression of inflammatory cytokines and phagocytic markers, which was associated with activation of p38 mitogen-activated protein kinase and Aβ internalization within microglia. Together, these studies challenge the “frustrated phagocytosis” concept and suggest that neuronal–microglial communication link the two central AD pathologies.

Original languageEnglish (US)
Pages (from-to)12538-12546
Number of pages9
JournalJournal of Neuroscience
Volume34
Issue number37
DOIs
StatePublished - Sep 10 2014
Externally publishedYes

Fingerprint

Microglia
p38 Mitogen-Activated Protein Kinases
Amyloid
Microtubule-Associated Proteins
Pathology
Membranes
Phagocytosis
Alzheimer Disease
Phosphorylation
Cyclic AMP-Dependent Protein Kinases
Protein Isoforms
Communication
Genotype
Cytokines
Ligands
Phenotype
Genes

Keywords

  • Alzheimer’s disease
  • CX3CL1
  • Microglia
  • Phagocytosis

ASJC Scopus subject areas

  • Neuroscience(all)
  • Medicine(all)

Cite this

Opposing effects of membrane-anchored CX3CL1 on amyloid and tau pathologies via the p38 MAPK pathway. / Lee, Sungho; Xu, Guixiang; Jay, Taylor R.; Ransohoff, Richard M.; Lamb, Bruce; Bhatta, Sabina; Lamb, Bruce T.; Landreth, Gary E.; Lamb, Bruce T.; Jay, Taylor R.; Lee, Sungho; Kim, Ki Wook; Jung, Steffen.

In: Journal of Neuroscience, Vol. 34, No. 37, 10.09.2014, p. 12538-12546.

Research output: Contribution to journalArticle

Lee, S, Xu, G, Jay, TR, Ransohoff, RM, Lamb, B, Bhatta, S, Lamb, BT, Landreth, GE, Lamb, BT, Jay, TR, Lee, S, Kim, KW & Jung, S 2014, 'Opposing effects of membrane-anchored CX3CL1 on amyloid and tau pathologies via the p38 MAPK pathway', Journal of Neuroscience, vol. 34, no. 37, pp. 12538-12546. https://doi.org/10.1523/JNEUROSCI.0853-14.2014
Lee, Sungho ; Xu, Guixiang ; Jay, Taylor R. ; Ransohoff, Richard M. ; Lamb, Bruce ; Bhatta, Sabina ; Lamb, Bruce T. ; Landreth, Gary E. ; Lamb, Bruce T. ; Jay, Taylor R. ; Lee, Sungho ; Kim, Ki Wook ; Jung, Steffen. / Opposing effects of membrane-anchored CX3CL1 on amyloid and tau pathologies via the p38 MAPK pathway. In: Journal of Neuroscience. 2014 ; Vol. 34, No. 37. pp. 12538-12546.
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