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Amyloidβneurotoxicity is IDO1–Kyn–AhR dependent and blocked by IDO1 inhibitor

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摘要 Dear Editor,Alzheimer’s disease(AD),the most common neurodegenerative disorder and a leading cause of dementia is characterized by progressive memory deficits,cognitive impairment and personality changes.The accumulation of extracellular amyloid beta(Aβ)plaques consisted by Aβpeptide and intracellular neurofibrillary tangles(NFTs)composed by misfolded hyperphosphorylated tau are main pathological hallmarks of AD,which ultimately lead to the dysfunction and loss of synapses and the eventual death of neuron.Neuroinflammation plays a causal role in AD pathogenesis.While the mechanism underlying neuroinflammationinduced AD pathology has not been fully elucidated,increasing evidence proposed that the kynurenine pathway(KP),a major route for L-tryptophan(L-Trp)catabolism,plays an important role.
出处 《Signal Transduction and Targeted Therapy》 SCIE CSCD 2020年第1期1633-1635,共3页 信号转导与靶向治疗(英文)
基金 supported by the Key Biomedical Program of Shanghai(Nos.17431902200 and 18431902600)and Shanghai Municipal Science and Technology Major Project(No.2018SHZDZX01)and ZJLab.
关键词 TAU ALZHEIMER
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