
NCBI . NLM . NIH . GOV {
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Title[redir]:
TREM2 haplodeficiency in mice and humans impairs the microglia barrier function leading to decreased amyloid compaction and severe axonal dystrophy - PMC
Description:
Haplodeficiency of the microglia gene TREM2 increases risk for late-onset Alzheimerโs disease (AD) but the mechanisms remain uncertain. To investigate this, we used high-resolution confocal and super-resolution (STORM) microscopy in AD-like mice and ...
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Keywords {๐}
microglia, trem, plaques, doi, mice, plaque, amyloid, figure, processes, pubmed, google, scholar, barrier, pmc, fibrils, filamentous, compact, article, dap, free, human, dystrophy, brain, individual, axonal, disease, deficiency, function, surface, degree, images, diffuse, alzheimers, increased, quantification, confocal, observed, thioflavin, fibril, mutations, xfad, total, humans, neurites, compaction, condello, core, imaging, risk, storm,
Topics {โ๏ธ}
n-terminus anti-aฮฒ antibody genome-wide gene-expression analysis light-induced dark states {beta}-stimulated microglial activation pmc beta search experimental procedures animals post-mortem temporal cortices multicolor time-stamp reveals abeta42-driven cerebral amyloidosis 642nm solid-state laser large late-onset family super-resolution storm imaging neuritic tau hyper-phosphorylation performed super-resolution nanoscopy positron emission tomography late-onset human ad intraneuronal beta-amyloid aggregates cd68-immunolabeled microglial phagosomes atomic-force microscopy data middle frontal gyrus postmortem human brain human brain tissue hyper-phosphorylated dystrophic neurites lamp1-immunolabeled axonal dystrophy fibrils extending radially common nasu-hakola disease 50mm sodium citrate postmortem human brains high-resolution confocal poor antibody penetration strong anti-colocalization human brain tissues dap12-deficient mice fail higher protofibrillar aฮฒ42 olmos-alonso iba1-labeled surrounding microglia cross-section fluorescence intensity human ad tissue mouse somatosensory cortex increased orthogonal branches branched aฮฒ nanostructures human tissue staining altered microglial response examined microglia-plaque interactions reactive oxygen species impaired antigen priming supplementary materials included rapid plaque growth single aฮฒ fibrils atomic-force microscopy
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