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PubMed:22427674 JSONTXT 24 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 0-128 Sentence denotes Apolipoprotein E3 (ApoE3) but not ApoE4 protects against synaptic loss through increased expression of protein kinase C epsilon.
T2 129-289 Sentence denotes Synaptic loss is the earliest pathological change in Alzheimer disease (AD) and is the pathological change most directly correlated with the degree of dementia.
T3 290-395 Sentence denotes ApoE4 is the major genetic risk factor for the age-dependent form of AD, which accounts for 95% of cases.
T4 396-597 Sentence denotes Here we show that in synaptic networks formed from primary hippocampal neurons in culture, apoE3, but not apoE4, prevents the loss of synaptic networks produced by amyloid β oligomers (amylospheroids).
T5 598-876 Sentence denotes Specific activators of PKCε, such as 8-(2-(2-pentyl-cyclopropylmethyl)-cyclopropyl)-octanoic acid methyl ester and bryostatin 1, protected against synaptic loss by amylospheroids, whereas PKCε inhibitors blocked this synaptic protection and also blocked the protection by apoE3.
T6 877-971 Sentence denotes Blocking LRP1, an apoE receptor on the neuronal membrane, also blocked the protection by apoE.
T7 972-1064 Sentence denotes ApoE3, but not apoE4, induced the synthesis of PKCε mRNA and expression of the PKCε protein.
T8 1065-1155 Sentence denotes Amyloid β specifically blocked the expression of PKCε but had no effect on other isoforms.
T9 1156-1274 Sentence denotes These results suggest that protection against synaptic loss by apoE is mediated by a novel intracellular PKCε pathway.
T10 1275-1397 Sentence denotes This apoE pathway may account for much of the protective effect of apoE and reduced risk for the age-dependent form of AD.
T11 1398-1482 Sentence denotes This finding supports the potential efficacy of newly developed therapeutics for AD.