淀粉样蛋白毒性引发的炎症反应被大麻素所阻断

IF 4.1 Q2 GERIATRICS & GERONTOLOGY
npj aging Pub Date : 2016-06-23 DOI:10.1038/npjamd.2016.12
Antonio Currais, Oswald Quehenberger, Aaron M Armando, Daniel Daugherty, Pam Maher, David Schubert
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引用次数: 56

摘要

大脑中的β淀粉样蛋白(Aβ)和其他聚集蛋白会随着年龄的增长而增加,并经常出现在神经元内。然而,人们对细胞内淀粉样蛋白、衰老和神经退行性变之间的机理关系并不十分清楚。我们利用一种基于在人类中枢神经系统神经细胞系中诱导性表达 Aβ 的蛋白毒性模型,描述了细胞内 Aβ 导致神经细胞死亡的一种独特形式。研究表明,细胞内 Aβ 引发了毒性炎症反应,导致细胞死亡。A β会诱导多种促炎基因的表达,并增加花生四烯酸和类二十酸,包括具有神经保护作用的前列腺素和加剧死亡的白三烯。大麻素(如四氢大麻酚)可刺激神经元内 Aβ的清除,阻断炎症反应,并具有保护作用。总之,这些数据表明,由于细胞内 Aβ 的积累,神经细胞内存在一种复杂的、可能是自催化的炎症反应,而这种早期形式的蛋白毒性可以通过激活大麻素受体来阻断。阻断神经元炎症的大麻素和其他药物有助于阻止阿尔茨海默氏症的发展。这种神经退行性疾病的特征之一是淀粉样β蛋白在脑细胞内聚集成块。美国索尔克生物研究所的戴维-舒伯特领导的研究人员利用组织培养模型来研究这些蛋白质聚集体的毒性作用。他们确定,淀粉样蛋白-β的产生会引发炎症反应,最终导致神经元死亡。不过,研究人员也发现了重要的保护机制。例如,大脑会产生一种叫做内源性大麻素的化合物,有助于消除淀粉样蛋白-β。使用四氢大麻酚--大麻的活性成分--等相关化合物进行治疗,也能减少炎症反应,防止细胞死亡,这为预防这种毁灭性疾病造成的神经损伤提供了潜在的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Amyloid proteotoxicity initiates an inflammatory response blocked by cannabinoids

Amyloid proteotoxicity initiates an inflammatory response blocked by cannabinoids
The beta amyloid (Aβ) and other aggregating proteins in the brain increase with age and are frequently found within neurons. The mechanistic relationship between intracellular amyloid, aging and neurodegeneration is not, however, well understood. We use a proteotoxicity model based upon the inducible expression of Aβ in a human central nervous system nerve cell line to characterize a distinct form of nerve cell death caused by intracellular Aβ. It is shown that intracellular Aβ initiates a toxic inflammatory response leading to the cell''s demise. Aβ induces the expression of multiple proinflammatory genes and an increase in both arachidonic acid and eicosanoids, including prostaglandins that are neuroprotective and leukotrienes that potentiate death. Cannabinoids such as tetrahydrocannabinol stimulate the removal of intraneuronal Aβ, block the inflammatory response, and are protective. Altogether these data show that there is a complex and likely autocatalytic inflammatory response within nerve cells caused by the accumulation of intracellular Aβ, and that this early form of proteotoxicity can be blocked by the activation of cannabinoid receptors. Cannabinoids and other drugs that block inflammation in neurons could help thwart the progression of Alzheimer‘s disease. One of the hallmarks of this neurodegenerative disorder is the accumulation of clumps of amyloid-β protein within brain cells. Researchers led by David Schubert of the Salk Institute for Biological Studies in the USA used a tissue culture model to study the toxic effects of these protein aggregates. They determined that the production of amyloid-β initiates an inflammatory response that ultimately leads to neuronal death. However, the researchers also identified important protective mechanisms. For example, the brain produces compounds called endocannabinoids that help eliminate amyloid-β. Treatment with related chemical compounds like tetrahydrocannabinol–the active ingredient in marijuana–also reduced inflammation and prevented cell death, suggesting a potential avenue for preventing neurological damage from this devastating disease.
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