| Literature DB >> 25286194 |
Xiaobei Zhao1, Yue Zhou2, April M Weissmiller1, Matthew L Pearn3, William C Mobley1, Chengbiao Wu4.
Abstract
BDNF plays an important role in several facets of neuronal survival, differentiation, and function. Structural and functional deficits in axons are increasingly viewed as an early feature of neurodegenerative diseases, including Alzheimer's disease (AD) and Huntington's disease (HD). As yet unclear is the mechanism(s) by which axonal injury is induced. We reported the development of a novel technique to produce biologically active, monobiotinylated BDNF (mBtBDNF) that can be used to trace axonal transport of BDNF. Quantum dot-labeled BDNF (QD-BDNF) was produced by conjugating quantum dot 655 to mBtBDNF. A microfluidic device was used to isolate axons from neuron cell bodies. Addition of QD-BDNF to the axonal compartment allowed live imaging of BDNF transport in axons. We demonstrated that QD-BDNF moved essentially exclusively retrogradely, with very few pauses, at a moving velocity of around 1.06 μm/sec. This system can be used to investigate mechanisms of disrupted axonal function in AD or HD, as well as other degenerative disorders.Entities:
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Year: 2014 PMID: 25286194 PMCID: PMC4828072 DOI: 10.3791/51899
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355