Journal Article

Microglial activation and tau propagate jointly across Braak stages

Gauthier, Serge, Savard, Melissa, Mathotaarachchi, Sulantha, Massarweh, Gassan, Edison, Paul, Zetterberg, Henrik, Stevenson, Jenna, Tissot, Cécile, Rosa-Neto, Pedro, Pascoal, Tharick A., Soucy, Jean-Paul, Chamoun, Mira, Kang, Min Su, Blennow, Kaj, Karikari, Thomas K., Benedet, Andrea L., Ottoy, Julie, Lussier, Firoza Z., Ashton, Nicholas J., Therriault, Joseph, Schöll, Michael, de Leon, Mony J.

2021

Overview

Compelling experimental evidence suggests that microglial activation is involved in the spread of tau tangles over the neocortex in Alzheimer’s disease (AD). We tested the hypothesis that the spatial propagation of microglial activation and tau accumulation colocalize in a Braak-like pattern in the living human brain. We studied 130 individuals across the aging and AD clinical spectrum with positron emission tomography brain imaging for microglial activation ([ 11 C]PBR28), amyloid-β (Aβ) ([ 18 F]AZD4694) and tau ([ 18 F]MK-6240) pathologies. We further assessed microglial triggering receptor expressed on myeloid cells 2 ( TREM2 ) cerebrospinal fluid (CSF) concentrations and brain gene expression patterns. We found that [ 11 C]PBR28 correlated with CSF soluble TREM2 and showed regional distribution resembling TREM2 gene expression. Network analysis revealed that microglial activation and tau correlated hierarchically with each other following Braak-like stages. Regression analysis revealed that the longitudinal tau propagation pathways depended on the baseline microglia network rather than the tau network circuits. The co-occurrence of Aβ, tau and microglia abnormalities was the strongest predictor of cognitive impairment in our study population. Our findings support a model where an interaction between Aβ and activated microglia sets the pace for tau spread across Braak stages. Microglial activation and tau accumulation propagate together in patients with Alzheimer’s disease, suggesting an interaction that determines disease progression.

• Publisher: Nature Publishing Group US,Nature Publishing Group
• Subject: 631/1647/245/2092 / 692/699/375/132/1283 / Abnormalities / Accumulation / Aging / Alzheimer's disease / Amyloid / Biomedical and Life Sciences / Biomedicine / Brain / Cancer Research / Cerebral cortex / Cerebrospinal fluid / Cognitive ability / Development and progression / Diagnosis / Fluorine isotopes / Gene expression / Health aspects / Infectious Diseases / Metabolic Diseases / Microglia / Molecular Medicine / Myeloid cells / Neocortex / Network analysis / Neurodegenerative diseases / Neuroimaging / Neurologi / Neurology / Neurosciences / Neurovetenskaper / Physiological aspects / Population studies / Positron emission / Positron emission tomography / Propagation / Regression analysis / Tau protein / Tau proteins