Cited by 221Neuroinflammation and Neurodegeneration MechanismsAlzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

TREM2 and the neuroimmunology of Alzheimer's disease

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Hickman, Suzanne E., El Khoury, Joseph·2014·Biochemical Pharmacology

Abstract

Late-onset Alzheimer's disease (AD) is a sporadic disorder with increasing prevalence in aging. The ɛ4 allele of Apolipoprotein E(ApoEɛ4) was the only known major risk factor for late onset AD. Recently, two groups of investigators independently identified variants of the TREM2 gene, encoding triggering receptor expressed on myeloid cells 2 as causing increased susceptibility to late onset AD with an odds ratio similar to that of ApoEɛ4. TREM2 is a receptor expressed on innate immune cells. Using a novel technology called Direct RNA Sequencing wedetermined the quantitative transcriptome of microglia, the principal innate neuroimmune cells and confirmed that TREM2 is a major microglia-specific gene in the central nervous system. Over the past several years we have shown that microglia play a dichotomous role in AD. Microglia can be protective and promote phagocytosis, degradation and ultimately clearance of Aβ, the pathogenic protein deposited in the brains of Alzheimer's patients. However, with disease progression, microglia become dysfunctional, release neurotoxins, lose their ability to clear Aβ and produce pro-inflammatory cytokines that promote Aβ production and accumulation. TREM2 has been shown to regulate the phagocytic ability of myeloid cells and their inflammatory response. Here we propose that the mechanism(s) by which TREM2 variants cause Alzheimer's disease are via down regulation of the Aβ phagocytic ability of microglia and by dysregulation of the pro-inflammatory response of these cells. Based on our discussion we propose that TREM2 is a potential therapeutic target for stopping ordelaying progression of AD.

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Authors
Hickman, S. E., & El Khoury, J.
Affiliations
Harvard University (US)
Venue
Biochemical Pharmacology
Publisher
Elsevier BV
Published
2014-04
Volume
88
Issue
4
Pages
495-498
ISSN
0006-2952 (ISSN-L)
OpenAlex
W2070847731
Cited by
221
References
48
Citations by year
2026: 8 · 2025: 17 · 2024: 18 · 2023: 10 · 2022: 20 · 2021: 14 · 2020: 14 · 2019: 19 · 2018: 25 · 2017: 28 · 2016: 19 · 2015: 16 · 2014: 13
FWCI
1.55
Type
journal article
Language
en
Open access
Locations
  • Biochemical Pharmacology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • NINDS (NS059005)
  • NIA to JEK (AG032349)
Topics
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
Keywords
TREM2, Alzheimer's disease, late-onset Alzheimer's disease, microglia, neuroimmunology, amyloid-beta clearance, phagocytosis, innate immunity, APOE ε4, genetic risk factors, inflammatory cytokines, therapeutic target
MeSH terms
Alzheimer Disease, Humans, Membrane Glycoproteins, Phagocytes, Receptors, Immunologic, Risk Factors, Amyloid beta-Peptides, Microglia, Genetic Predisposition to Disease

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