Abstract
Deciphering the targets of axonal projections plays a pivotal role in interpreting neuronal function and pathology. Neuronal tracers are indispensable tools for uncovering the functions and interactions between different subregions of the brain. However, the selection of commercially available neuronal tracers is limited, currently comprising small molecule dyes, viruses, and a handful of synthetic nanoparticles. Here, we describe a series of polymer-based nanoparticles capable of retrograde transport along neurons in vivo in mice. These polymeric nanoparticle neuronal tracers (NNTs) are prepared with a palette of fluorescent labels. The morphologies, charges, and optical properties of NNTs are characterized by analytical methods including fluorescence microscopy, electron microscopy, and dynamic light scattering. Cytotoxicity and cellular uptake were investigated to analyze cellular interactions in vitro. Regardless of the type of fluorophore used in labeling, each tracer was of similar morphology, size, and charge and was competent for retrograde transport in vivo. The platform provides a convenient, scalable synthetic approach for nonviral tracers labeled with a range of fluorophores for in vivo neuronal projection mapping.
Original language | English (US) |
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Pages (from-to) | 436-445 |
Number of pages | 10 |
Journal | ACS Central Science |
Volume | 6 |
Issue number | 3 |
DOIs | |
State | Published - Mar 25 2020 |
Funding
N.Z. designed the research and analyzed the data. T.B.D. designed the Cy5.5 dye synthetic route. N.Z. performed synthetic, biochemical, and imaging and drafted the paper. J.B.I. performed direct intracranial injections and surgeries. M.A.T. performed cryo-EM. D.S.B. and A.M.R. contributed to the original idea and preliminary studies. N.C.G. and D.A.D. provided financial support. N.C.G., D.A.D., and M.S. directed the research. All authors edited the manuscript.
ASJC Scopus subject areas
- General Chemistry
- General Chemical Engineering