Highly sensitive Curcumin-conjugated nanotheranostic platform for detecting amyloid-beta plaques by magnetic resonance imaging and reversing cognitive deficits of Alzheimer's disease via NLRP3-inhibition.
Highly sensitive Curcumin-conjugated nanotheranostic platform for detecting amyloid-beta plaques by magnetic resonance imaging and reversing cognitive deficits of Alzheimer's disease via NLRP3-inhibition.
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高灵敏度姜黄素偶联纳米治疗平台,用于通过磁共振成像检测淀粉样蛋白斑块,并通过 NLRP3 抑制逆转阿尔茨海默病的认知缺陷
DOI:
10.1186/s12951-022-01524-4
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发表时间:
2022-07-14
影响因子:
10.2
通讯作者:
Liu, Jun
中科院分区:
文献类型:
--
作者:
Ruan, Yuting;Xiong, Ying;Fang, Wenli;Yu, Qun;Mai, Yingren;Cao, Zhiyu;Wang, Kexi;Lei, Ming;Xu, Jiaxin;Liu, Yan;Zhang, Xingcai;Liao, Wang;Liu, Jun
Alzheimer's disease (AD) is the most common neurodegenerative disorder without effective therapy and lack diagnosis strategy for preclinical AD patients. There is an urgent need for development of both early diagnosis and therapeutic intervention of AD. Herein, we developed a nanotheranostics platform consisting of Curcumin (Cur), an anti-inflammatory molecule, and superparamagnetic iron oxide (SPIO) nanoparticles encapsulated by diblock 1,2-dio-leoyl-sn-glycero-3-phosphoethanolamine-n-[poly(ethylene glycol)] (DSPE-PEG) that are modified with CRT and QSH peptides on its surface. Furthermore, we demonstrated that this multifunctional nanomaterial efficiently reduced β-amyloid plaque burden specifically in APP/PS1 transgenic mice, with the process noninvasively detected by magnetic resonance imaging (MRI) and the two-dimensional MRI images were computed into three-dimension (3D) plot. Our data demonstrated highly sensitive in vivo detection of β-amyloid plaques which more closely revealed real deposition of Aβ than previously reported and we quantified the volumes of plaques for the first time based on 3D plot. In addition, memory deficits of the mice were significantly rescued, probably related to inhibition of NLR Family Pyrin Domain Containing 3 (NLRP3) inflammasomes. Gathered data demonstrated that this theranostic platform may have both early diagnostic and therapeutic potential in AD. The online version contains supplementary material available at 10.1186/s12951-022-01524-4.
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影响因子:
64.8
作者:
通讯作者:
--
影响因子:
8.8
作者:
Friker LL;Scheiblich H;Hochheiser IV;Brinkschulte R;Riedel D;Latz E;Geyer M;Heneka MT
通讯作者:
Heneka MT
影响因子:
6
作者:
Fahmy AM;El-Setouhy DA;Ibrahim AB;Habib BA;Tayel SA;Bayoumi NA
通讯作者:
Bayoumi NA
影响因子:
14
作者:
Boccafoschi, F;Habermehl, J;Mantovani, D
通讯作者:
Mantovani, D
影响因子:
3.6
作者:
Kannan, Ramalingam G.;Abhilash, Maliakal B.;Krishnakumar, I. M.
通讯作者:
Krishnakumar, I. M.