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本文引用的文献

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Arginyltransferase ATE1 is targeted to the neuronal growth cones and regulates neurite outgrowth during brain development.精氨酰转移酶ATE1定位于神经元生长锥,并在大脑发育过程中调节神经突生长。
Dev Biol. 2017 Oct 1;430(1):41-51. doi: 10.1016/j.ydbio.2017.08.027. Epub 2017 Aug 26.
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The acute inhibition of enteric glial metabolism with fluoroacetate alters calcium signaling, hemichannel function, and the expression of key proteins.用氟乙酸对肠神经胶质细胞代谢进行急性抑制会改变钙信号传导、半通道功能以及关键蛋白的表达。
J Neurophysiol. 2017 Jan 1;117(1):365-375. doi: 10.1152/jn.00507.2016. Epub 2016 Oct 26.
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Ablation of Arg-tRNA-protein transferases results in defective neural tube development.精氨酸 - 转运RNA - 蛋白质转移酶的缺失导致神经管发育缺陷。
BMB Rep. 2016 Aug;49(8):443-8. doi: 10.5483/bmbrep.2016.49.8.087.
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Post-translational protein arginylation in the normal nervous system and in neurodegeneration.正常神经系统和神经退行性变中的蛋白质翻译后精氨酰化
J Neurochem. 2016 Aug;138(4):506-17. doi: 10.1111/jnc.13708. Epub 2016 Jul 5.
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Mitochondria-Targeting Ceria Nanoparticles as Antioxidants for Alzheimer's Disease.线粒体靶向性二氧化铈纳米颗粒作为阿尔茨海默病的抗氧化剂
ACS Nano. 2016 Feb 23;10(2):2860-70. doi: 10.1021/acsnano.5b08045. Epub 2016 Feb 10.
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Effect of PLGA NP size on efficiency to target traumatic brain injury.PLGA NP 粒径对靶向创伤性脑损伤效率的影响。
J Control Release. 2016 Feb 10;223:31-41. doi: 10.1016/j.jconrel.2015.12.029. Epub 2015 Dec 18.
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New formulation of old aspirin for better delivery.老药阿司匹林的新配方,实现更好的给药效果。
Chem Commun (Camb). 2016 Jan 4;52(1):140-3. doi: 10.1039/c5cc07316b.
8
Evaluation of nanoparticle delivered cisplatin in beagles.犬体内载顺铂纳米颗粒的评价。
Nanoscale. 2015 Sep 7;7(33):13822-30. doi: 10.1039/c5nr03447g.
9
Lipophilic triphenylphosphonium cations inhibit mitochondrial electron transport chain and induce mitochondrial proton leak.亲脂性三苯基鏻阳离子抑制线粒体电子传递链并诱导线粒体质子泄漏。
PLoS One. 2015 Apr 30;10(4):e0121837. doi: 10.1371/journal.pone.0121837. eCollection 2015.
10
Poly (D,L-lactide-co-glycolide) nanoparticles loaded with cerebrolysin display neuroprotective activity in a rat model of concussive head injury.载有脑活素的聚(D,L-丙交酯-共-乙交酯)纳米颗粒在大鼠脑震荡损伤模型中显示出神经保护活性。
CNS Neurol Disord Drug Targets. 2014;13(8):1475-82. doi: 10.2174/1871527313666140806145540.

纳米技术介导的两种不可渗透膜的交叉以调节神经血管单元的星形胶质细胞来实现神经保护。

Nanotechnology-mediated crossing of two impermeable membranes to modulate the stars of the neurovascular unit for neuroprotection.

机构信息

Department of Biochemistry and Molecular Biology, Miller School of Medicine, University of Miami, Miami, FL 33136.

Department of Radiation Oncology, Miller School of Medicine, University of Miami, Miami, FL 33136.

出版信息

Proc Natl Acad Sci U S A. 2018 Dec 26;115(52):E12333-E12342. doi: 10.1073/pnas.1816429115. Epub 2018 Dec 10.

DOI:10.1073/pnas.1816429115
PMID:30530697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6310851/
Abstract

The success of nanoparticle-mediated delivery of antioxidant and antiinflammatory-based neuroprotectants to the brain to improve neuronal functions in neurodegenerative diseases has demonstrated lesser impact instead of achieving its full potential. We hypothesized that these failures were due to a combination of parameters, such as: () unavailability of a delivery vehicle, which can reproducibly and efficiently transport through the brain capillary endothelium; () inefficient uptake of therapeutic nanoparticles in the neuronal cell population; and () limited ability of a single nanoparticle to cross the two most-impermeable biological barriers, the blood-brain barrier and mitochondrial double membrane, so that a nanoparticle can travel through the brain endothelial barrier to the mitochondria of target cells where oxidative damage is localized. Herein, we demonstrate optimization of a biodegradable nanoparticle for efficient brain accumulation and protection of astrocytes from oxidative damage and mitochondrial dysfunctions to enhance the neuroprotection ability of astrocytes toward neurons using neurodegeneration characteristics in SOD1 rats. This biodegradable nanomedicine platform with the ability to accumulate in the brain has the potential to bring beneficial effects in neurodegenerative diseases by modulating the stars, astrocytes in the brain, to enhance their neuroprotective actions.

摘要

纳米颗粒介导的抗氧化和抗炎神经保护剂递送至大脑以改善神经退行性疾病中的神经元功能的成功,已经证明其影响较小,而未能发挥其全部潜力。我们假设这些失败是由于多种因素的综合作用,例如:(1)缺乏能够可重复且有效地穿过脑毛细血管内皮的递药载体;(2)治疗性纳米颗粒在神经元细胞群体中的摄取效率低下;以及(3)单个纳米颗粒穿过两个最不易渗透的生物屏障(血脑屏障和线粒体双层膜)的能力有限,因此纳米颗粒可以通过脑内皮屏障到达目标细胞的线粒体,而氧化损伤定位于该处。在此,我们证明了可生物降解纳米颗粒的优化,以有效积累并保护星形胶质细胞免受氧化损伤和线粒体功能障碍,从而增强星形胶质细胞对神经元的神经保护作用,利用 SOD1 大鼠的神经退行性变特征。这种具有在大脑中积累能力的生物可降解纳米医学平台,通过调节大脑中的“明星”——星形胶质细胞,有可能在神经退行性疾病中带来有益的效果,增强其神经保护作用。