科研之友
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摘要
Amyloid plaque is a prominent pathologic hallmark in the brains of patients with Alzheimer's disease (AD), and it has been shown to be associated with endoplasmic reticulum (ER) stress response. However the precise regulation mechanism of amyloid-beta (A beta) toxicity remains unclear. Here, we found that dauricine could activate X-box binding protein 1 (XBP-1; active form XBP-1S) and eukaryotic translation initiation factor eIF2 alpha and thus delay the progression of AD in the A beta(1-42)-transgenic Caenorhabditis elegans CL2120. The ER stress response factor XBP-1 can be activated and shows neuroprotective activity through acceleration of An clearance. Our study reveals that dauricine activates the ire-1 ixbp-1 and perk/e/IF2 alpha pathways of the unfolded protein response, attenuates translation, and enhances ER-associated degradation, which reduces A beta expression and attenuates An-associated toxicity. On the contrary, xbp-1 depletion counteracts the effects of dauricine on Apassociated toxicity. These results underscore the functional relevance of XBP-1 in An toxicity and degradation, and highlight the potentially pharmacodynamic value of dauricine in preventing the progression of AD.
