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西红花酸通过 STK11/LKB1 介导的 AMPK 通路诱导自噬促进淀粉样β清除。

Crocetin promotes clearance of amyloid-β by inducing autophagy via the STK11/LKB1-mediated AMPK pathway.

机构信息

Division of PK-PD-Toxicology and Formulation, CSIR-Indian Institute of Integrative Medicine, Jammu, India.

Academy of Scientific and Innovative Research (Acsir), Ghaziabad, India.

出版信息

Autophagy. 2021 Nov;17(11):3813-3832. doi: 10.1080/15548627.2021.1872187. Epub 2021 Jan 19.

Abstract

Alzheimer disease (AD) is usually accompanied by two prominent pathological features, cerebral accumulation of amyloid-β (Aβ) plaques and presence of MAPT/tau neurofibrillary tangles. Dysregulated clearance of Aβ largely contributes to its accumulation and plaque formation in the brain. Macroautophagy/autophagy is a lysosomal degradative process, which plays an important role in the clearance of Aβ. Failure of autophagic clearance of Aβ is currently acknowledged as a contributing factor to increased accumulation of Aβ in AD brains. In this study, we have identified crocetin, a pharmacologically active constituent from the flower stigmas of , as a potential inducer of autophagy in AD. In the cellular model, crocetin induced autophagy in N9 microglial and primary neuron cells through STK11/LKB1 (serine/threonine kinase 11)-mediated AMP-activated protein kinase (AMPK) pathway activation. Autophagy induction by crocetin significantly increased Aβ clearance in N9 cells. Moreover, crocetin crossed the blood-brain barrier and induced autophagy in the brains' hippocampi of wild-type male C57BL/6 mice. Further studies in transgenic male 5XFAD mice, as a model of AD, revealed that one-month treatment with crocetin significantly reduced Aβ levels and neuroinflammation in the mice brains and improved memory function by inducing autophagy that was mediated by AMPK pathway activation. Our findings support further development of crocetin as a pharmacological inducer of autophagy to prevent, slow down progression, and/or treat AD. Aβ: amyloid-β; ABCB1/P-gp/P-glycoprotein: ATP-binding cassette, subfamily B (MDR/TAP), member 1; AD: Alzheimer disease; AMPK/PRKAA: AMP-activated protein kinase; APP: amyloid beta (A4) precursor protein; ATG: autophagy related; BBB: blood-brain barrier; BECN1: beclin 1, autophagy related; CAMKK2/CaMKKβ: calcium/calmodulin-dependent protein kinase kinase 2, beta; CSE: Crocus sativus extract; CTSB: cathepsin B; EIF4EBP1: eukaryotic translation initiation factor 4E binding protein 1; GFAP: glial fibrillary acidic protein; GSK3B/GSK3β: glycogen synthase kinase 3 beta; Kp: brain partition coefficient; LRP1: low density lipoprotein receptor-related protein 1; MAP1LC3B/LC3B: microtubule-associated protein 1 light chain 3 beta; MAP2: microtubule-associated protein 2; MAPK/ERK: mitogen-activated protein kinase; MAPT/tau: microtubule-associated protein tau; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; MTOR: mechanistic target of rapamycin kinase; MWM: Morris water maze; NFKB/NF-κB: nuclear factor of kappa light polypeptide gene enhancer in B cells; NMDA: N-methyl-d-aspartic acid; RPTOR: regulatory associated protein of MTOR; RPS6KB1/p70S6K: ribosomal protein S6 kinase 1; SQSTM1: sequestosome 1; SRB: sulforhodamine B; STK11/LKB1: serine/threonine kinase 11; TFEB: transcription factor EB; TSC2: TSC complex subunit 2; ULK1: unc-51 like kinase 1.

摘要

阿尔茨海默病(AD)通常伴随着两个突出的病理特征,即大脑中淀粉样β(Aβ)斑块的积累和 MAPT/tau 神经原纤维缠结的存在。Aβ 的清除失调在很大程度上导致了其在大脑中的积累和斑块形成。巨自噬/自噬是溶酶体降解过程,在 Aβ 的清除中起着重要作用。目前认为自噬清除 Aβ 的失败是导致 AD 大脑中 Aβ 积累增加的一个因素。在这项研究中,我们已经确定藏红花酸,一种来自藏红花柱头的药理学活性成分,作为 AD 中自噬的潜在诱导剂。在细胞模型中,藏红花酸通过 STK11/LKB1(丝氨酸/苏氨酸激酶 11)介导的 AMP 激活蛋白激酶(AMPK)通路激活,诱导 N9 小胶质细胞和原代神经元细胞中的自噬。藏红花酸诱导的自噬显著增加了 N9 细胞中的 Aβ 清除。此外,藏红花酸穿过血脑屏障,在野生型雄性 C57BL/6 小鼠的海马中诱导自噬。在 AD 模型的转基因雄性 5XFAD 小鼠中的进一步研究表明,用藏红花酸治疗一个月可显著降低小鼠大脑中的 Aβ 水平和神经炎症,并通过 AMPK 通路激活诱导自噬来改善记忆功能。我们的研究结果支持进一步开发藏红花酸作为自噬的药理学诱导剂,以预防、减缓进展和/或治疗 AD。Aβ:淀粉样β;ABCB1/P-gp/P-糖蛋白:ATP 结合盒,亚家族 B(MDR/TAP),成员 1;AD:阿尔茨海默病;AMPK/PRKAA:AMP 激活蛋白激酶;APP:淀粉样前体蛋白;ATG:自噬相关;BBB:血脑屏障;BECN1:自噬相关蛋白 1;CAMKK2/CaMKKβ:钙/钙调蛋白依赖性蛋白激酶激酶 2,β;CSE:藏红花提取物;CTSB:组织蛋白酶 B;EIF4EBP1:真核翻译起始因子 4E 结合蛋白 1;GFAP:神经胶质纤维酸性蛋白;GSK3B/GSK3β:糖原合成酶激酶 3β;Kp:脑分配系数;LRP1:低密度脂蛋白受体相关蛋白 1;MAP1LC3B/LC3B:微管相关蛋白 1 轻链 3β;MAP2:微管相关蛋白 2;MAPK/ERK:丝裂原激活蛋白激酶;MAPT/tau:微管相关蛋白 tau;MTT:3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐;MTOR:雷帕霉素靶蛋白激酶;MWM:莫里斯水迷宫;NFKB/NF-κB:B 细胞中κ 轻肽基因增强子核因子;NMDA:N-甲基-D-天冬氨酸;RPTOR:MTOR 相关调节蛋白;RPS6KB1/p70S6K:核糖体蛋白 S6 激酶 1;SQSTM1:自噬体 1;SRB:磺基罗丹明 B;STK11/LKB1:丝氨酸/苏氨酸激酶 11;TFEB:转录因子 EB;TSC2:TSC 复合物亚基 2;ULK1:unc-51 样激酶 1。

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