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纳米颗粒介导的信号转导内体定位调节生长锥运动和神经突生长。

Nanoparticle-mediated signaling endosome localization regulates growth cone motility and neurite growth.

机构信息

Bascom Palmer Eye Institute, Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

出版信息

Proc Natl Acad Sci U S A. 2011 Nov 22;108(47):19042-7. doi: 10.1073/pnas.1019624108. Epub 2011 Nov 7.

Abstract

Understanding neurite growth regulation remains a seminal problem in neurobiology. During development and regeneration, neurite growth is modulated by neurotrophin-activated signaling endosomes that transmit regulatory signals between soma and growth cones. After injury, delivering neurotrophic therapeutics to injured neurons is limited by our understanding of how signaling endosome localization in the growth cone affects neurite growth. Nanobiotechnology is providing new tools to answer previously inaccessible questions. Here, we show superparamagnetic nanoparticles (MNPs) functionalized with TrkB agonist antibodies are endocytosed into signaling endosomes by primary neurons that activate TrkB-dependent signaling, gene expression and promote neurite growth. These MNP signaling endosomes are trafficked into nascent and existing neurites and transported between somas and growth cones in vitro and in vivo. Manipulating MNP-signaling endosomes by a focal magnetic field alters growth cone motility and halts neurite growth in both peripheral and central nervous system neurons, demonstrating signaling endosome localization in the growth cone regulates motility and neurite growth. These data suggest functionalized MNPs may be used as a platform to study subcellular organelle localization and to deliver nanotherapeutics to treat injury or disease in the central nervous system.

摘要

理解神经突生长调控仍然是神经生物学中的一个重要问题。在发育和再生过程中,神经突生长受到神经营养因子激活的信号内体的调节,这些信号内体在体和生长锥之间传递调节信号。在损伤后,向损伤神经元输送神经营养治疗方法受到我们对生长锥中信号内体定位如何影响神经突生长的理解的限制。纳米生物技术为回答以前无法解决的问题提供了新的工具。在这里,我们展示了用 TrkB 激动剂抗体功能化的超顺磁纳米颗粒 (MNP) 被原代神经元内吞到信号内体中,激活 TrkB 依赖性信号转导、基因表达,并促进神经突生长。这些 MNP 信号内体在体外和体内被运输到新生和现有的神经突中,并在体和生长锥之间运输。通过聚焦磁场操纵 MNP-信号内体改变生长锥的运动,并停止周围和中枢神经系统神经元的神经突生长,证明生长锥中信号内体的定位调节运动和神经突生长。这些数据表明,功能化的 MNPs 可用作研究亚细胞细胞器定位的平台,并向中枢神经系统输送纳米治疗药物以治疗损伤或疾病。

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