ER stress associated TXNIP-NLRP3 inflammasome activation in hippocampus of human Alzheimer's disease

• Published in: Neurochemistry international 2021-09, Vol.148, p.105104-105104, Article 105104
• Main Authors: Ismael, Saifudeen, Wajidunnisa, Sakata, Kazuko, McDonald, Michael P., Liao, Francesca-Fang, Ishrat, Tauheed
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - genetics; Alzheimer's disease; Biomarkers; CARD Signaling Adaptor Proteins - metabolism; Carrier Proteins - genetics; Caspase 1 - metabolism; Endoplasmic Reticulum Stress; Eukaryotic Initiation Factor-2; Female; Hippocampus - pathology; Humans; Inflammasomes; Interleukin-1beta - metabolism; Male; Middle Aged; NLR Family, Pyrin Domain-Containing 3 Protein - genetics; NLRP3 inflammasome; Thioredoxin-interacting protein; Transcription Factor CHOP - metabolism
• ISSN: 0197-0186; 1872-9754; 1872-9754
• DOI: 10.1016/j.neuint.2021.105104

Although the exact etiology of Alzheimer's disease (AD) is poorly understood, experimental and clinical evidences suggest the contribution of neuroinflammation in the pathogenesis of AD. Pathologically, AD brain is characterized by an imbalance in redox status, elevated endoplasmic reticulum (ER) stress, synaptic dysfunction, inflammation, and progressive neurodegeneration. It has been noted that continuous accumulation of amyloid-beta (Aβ) and intracellular neurofibrillary tangles (NFTs) in AD brain trigger ER stress, which contributes to neurodegeneration. Similarly, experimental evidences supports the hypothesis that thioredoxin-interacting protein (TXNIP), an endogenous regulator of redox regulator thioredoxin (TRX), is activated by ER stress and contributes to activation of NLRP3 (NOD-like receptor protein 3) inflammatory cascade in hippocampus of the AD brain. Hippocampus of postmortem human AD and aged matched non-AD controls were analyzed for the expression ER stress markers and TXNIP-NLRP3 inflammasome at cellular and molecular levels. We found higher expression of TXNIP at protein and transcript levels in close association with pathological markers of AD such as Aβ and NFTs in AD hippocampus. In addition, our results demonstrated that TXNIP was co-localized in neurons and microglia. Moreover, expression of binding immunoglobulin protein (BiP), activated eukaryotic initiation factor-2α (eIf2α) and C/EBP homology protein (CHOP), proteins involved the development of ER stress, were elevated in AD hippocampus. Further, elevated expression of effector molecules of NLRP3 inflammasome activation such as apoptosis associated speck-like protein (ASC), cleaved caspase-1 and cleaved interleukin-1β were observed in the AD hippocampus. The study suggests that TXNIP could be a link that connect ER stress with neuroinflammation. Thus, TXNIP can be a possible therapeutic target to mitigate the progression of neuroinflammation in the pathogenesis of AD. •AD upregulates ER-stress associated TXNIP/NLRP3 inflammasome in the human hippocampus.•TXNIP is co-localized neurons and microglia in human AD brain.•Inhibition of TXNIP can be a possible therapeutic target to mitigate neuroinflammation and AD pathology.