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本文引用的文献

1
Wild type alpha-synuclein is degraded by chaperone-mediated autophagy and macroautophagy in neuronal cells.野生型α-突触核蛋白在神经元细胞中通过伴侣介导的自噬和巨自噬被降解。
J Biol Chem. 2008 Aug 29;283(35):23542-56. doi: 10.1074/jbc.M801992200. Epub 2008 Jun 19.
2
Chaperone-mediated autophagy.伴侣介导的自噬
Methods Mol Biol. 2008;445:227-44. doi: 10.1007/978-1-59745-157-4_15.
3
The role of alpha-synuclein in neurodegenerative diseases: a potential target for new treatment strategies?α-突触核蛋白在神经退行性疾病中的作用:新治疗策略的潜在靶点?
Neurodegener Dis. 2008;5(3-4):218-21. doi: 10.1159/000113707. Epub 2008 Mar 6.
4
Protein misfolding and neurodegeneration.蛋白质错误折叠与神经退行性变。
Arch Neurol. 2008 Feb;65(2):184-9. doi: 10.1001/archneurol.2007.56.
5
The two faces of protein misfolding: gain- and loss-of-function in neurodegenerative diseases.蛋白质错误折叠的两面性:神经退行性疾病中的功能获得与功能丧失
EMBO J. 2008 Jan 23;27(2):336-49. doi: 10.1038/sj.emboj.7601930.
6
Tat-Hsp70 protects dopaminergic neurons in midbrain cultures and in the substantia nigra in models of Parkinson's disease.Tat-Hsp70可保护中脑培养物中的多巴胺能神经元以及帕金森病模型黑质中的多巴胺能神经元。
J Neurochem. 2008 May;105(3):853-64. doi: 10.1111/j.1471-4159.2007.05204.x. Epub 2007 Dec 24.
7
Specific AAV serotypes stably transduce primary hippocampal and cortical cultures with high efficiency and low toxicity.特定的腺相关病毒(AAV)血清型能高效且低毒地稳定转导原代海马体和皮质培养物。
Brain Res. 2008 Jan 23;1190:15-22. doi: 10.1016/j.brainres.2007.11.015. Epub 2007 Nov 17.
8
Nonviral approaches for neuronal delivery of nucleic acids.用于向神经元递送核酸的非病毒方法。
Pharm Res. 2008 May;25(5):983-98. doi: 10.1007/s11095-007-9439-5. Epub 2007 Oct 12.
9
High-efficiency transfection of mammalian neurons via nucleofection.通过核转染实现哺乳动物神经元的高效转染。
Nat Protoc. 2007;2(7):1692-704. doi: 10.1038/nprot.2007.226.
10
Solid lipid nanoparticles for targeted brain drug delivery.用于靶向脑内药物递送的固体脂质纳米粒
Adv Drug Deliv Rev. 2007 Jul 10;59(6):454-77. doi: 10.1016/j.addr.2007.04.011. Epub 2007 May 22.

使用聚合物纳米颗粒将功能性蛋白质递送至神经元。

Functional protein delivery into neurons using polymeric nanoparticles.

作者信息

Hasadsri Linda, Kreuter Jörg, Hattori Hiroaki, Iwasaki Tadao, George Julia M

机构信息

Department of Cell and Developmental Biology, College of Medicine, Medical Scholars Program, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, USA.

出版信息

J Biol Chem. 2009 Mar 13;284(11):6972-81. doi: 10.1074/jbc.M805956200. Epub 2009 Jan 7.

DOI:10.1074/jbc.M805956200
PMID:19129199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2652328/
Abstract

An efficient route for delivering specific proteins and peptides into neurons could greatly accelerate the development of therapies for various diseases, especially those involving intracellular defects such as Parkinson disease. Here we report the novel use of polybutylcyanoacrylate nanoparticles for delivery of intact, functional proteins into neurons and neuronal cell lines. Uptake of these particles is primarily dependent on endocytosis via the low density lipoprotein receptor. The nanoparticles are rapidly turned over and display minimal toxicity to cultured neurons. Delivery of three different functional cargo proteins is demonstrated. When primary neuronal cultures are treated with recombinant Escherichia coli beta-galactosidase as nanoparticle cargo, persistent enzyme activity is measured beyond the period of nanoparticle degradation. Delivery of the small GTPase rhoG induces neurite outgrowth and differentiation in PC12 cells. Finally, a monoclonal antibody directed against synuclein is capable of interacting with endogenous alpha-synuclein in cultured neurons following delivery via nanoparticles. Polybutylcyanoacrylate nanoparticles are thus useful for intracellular protein delivery in vitro and have potential as carriers of therapeutic proteins for treatment of neuronal disorders in vivo.

摘要

一种将特定蛋白质和肽递送至神经元的有效途径可极大地加速各种疾病治疗方法的开发,尤其是那些涉及细胞内缺陷的疾病,如帕金森病。在此,我们报告聚氰基丙烯酸丁酯纳米颗粒在将完整的功能性蛋白质递送至神经元和神经元细胞系方面的新用途。这些颗粒的摄取主要依赖于通过低密度脂蛋白受体的内吞作用。纳米颗粒能快速更新,且对培养的神经元显示出最小的毒性。文中展示了三种不同功能性负载蛋白的递送情况。当用重组大肠杆菌β-半乳糖苷酶作为纳米颗粒负载处理原代神经元培养物时,在纳米颗粒降解期之后仍可检测到持续的酶活性。小GTP酶rhoG的递送可诱导PC12细胞的神经突生长和分化。最后,一种针对突触核蛋白的单克隆抗体在通过纳米颗粒递送后能够与培养神经元中的内源性α-突触核蛋白相互作用。因此,聚氰基丙烯酸丁酯纳米颗粒可用于体外细胞内蛋白质递送,并具有作为治疗性蛋白质载体用于体内治疗神经元疾病的潜力。