The mechanism of tau toxicity is still unclear. Here we report that recombinant tau oligomers and monomers, intraventricularly injected in mice with a pure human tau background, foster tau pathology through different mechanisms. Oligomeric forms of tau alter the conformation of tau in a paired helical filament-like manner. This effect occurs without tau hyperphosphorylation as well as activation of specific kinases, suggesting that oligomers of tau induce tau assembly through a nucleation effect. Monomers, in turn, induce neurodegeneration through a calpain-mediated tau cleavage that leads to accumulation of a 17kDa neurotoxic peptide and induction of apoptotic cell death
Abnormal aggregation of protein tau and subsequent neuronal dysfunction seems to be key pathological...
Despite extensive structure-function analyses, the molecular mechanisms of normal and pathological t...
Different tauopathies are characterized by the isoform-specific composition of the aggregates found ...
Aggregation of highly phosphorylated tau is a hallmark of Alzheimer’s disease and other tauopathies....
Recent data from various experimental models support the link between extracellular tau and neurodeg...
In Alzheimer’s disease (AD), tau aggregates into fibrils and higher order neurofibrillary tangles, a...
TAU is a microtubule-associated protein that under pathological conditions such as Alzheimer’s disea...
Aggregation of highly-phosphorylated tau into aggregated forms such as filaments and neurofibrillary...
Abstract Background We have evaluated the efficacy of targeting the toxic, oligomeric form of tau pr...
The mechanistic relationship between amyloid \u3b21-42 (A\u3b21-42) and the alteration of Tau protei...
Tau misfolding and aggregation leads to the formation of neurofibrillary tangles (NFTs), which have ...
Hyperphosphorylated and aggregated tau protein constitutes the main pathological hallmark of tauopat...
Several neurodegenerative diseases are characterized by the aggregation and posttranslational modifi...
Tauopathies have diverse presentation, progression, and neuropathology. They are linked to tau prion...
Neurofibrillary tangles (NFTs) composed of intracellular aggregates of tau protein are a key neuropa...
Abnormal aggregation of protein tau and subsequent neuronal dysfunction seems to be key pathological...
Despite extensive structure-function analyses, the molecular mechanisms of normal and pathological t...
Different tauopathies are characterized by the isoform-specific composition of the aggregates found ...
Aggregation of highly phosphorylated tau is a hallmark of Alzheimer’s disease and other tauopathies....
Recent data from various experimental models support the link between extracellular tau and neurodeg...
In Alzheimer’s disease (AD), tau aggregates into fibrils and higher order neurofibrillary tangles, a...
TAU is a microtubule-associated protein that under pathological conditions such as Alzheimer’s disea...
Aggregation of highly-phosphorylated tau into aggregated forms such as filaments and neurofibrillary...
Abstract Background We have evaluated the efficacy of targeting the toxic, oligomeric form of tau pr...
The mechanistic relationship between amyloid \u3b21-42 (A\u3b21-42) and the alteration of Tau protei...
Tau misfolding and aggregation leads to the formation of neurofibrillary tangles (NFTs), which have ...
Hyperphosphorylated and aggregated tau protein constitutes the main pathological hallmark of tauopat...
Several neurodegenerative diseases are characterized by the aggregation and posttranslational modifi...
Tauopathies have diverse presentation, progression, and neuropathology. They are linked to tau prion...
Neurofibrillary tangles (NFTs) composed of intracellular aggregates of tau protein are a key neuropa...
Abnormal aggregation of protein tau and subsequent neuronal dysfunction seems to be key pathological...
Despite extensive structure-function analyses, the molecular mechanisms of normal and pathological t...
Different tauopathies are characterized by the isoform-specific composition of the aggregates found ...