Hasadsri Linda, Kreuter Jörg, Hattori Hiroaki, Iwasaki Tadao, George Julia M
Department of Cell and Developmental Biology, College of Medicine, Medical Scholars Program, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, USA.
J Biol Chem. 2009 Mar 13;284(11):6972-81. doi: 10.1074/jbc.M805956200. Epub 2009 Jan 7.
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.
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。