Neural Tracing Protein-Functionalized Nanoparticles Capable of Fast Retrograde Axonal Transport in Live Neurons.
Wenqian WangMd Musfizur HassanNatasha Kapoor-KaushikLital LivniBenjamin MusrieJianbo TangZaheri MahmudSaluo LaiPeter Richard WichVaishnavi AnanthanarayananGila Moalem-TaylorGuangzhao MaoPublished in: Small (Weinheim an der Bergstrasse, Germany) (2024)
Neural tracing proteins like horseradish peroxidase-conjugated wheat germ agglutinin (WGA-HRP) can target the central nervous system (CNS) through anatomic retrograde transport without crossing the blood-brain barrier (BBB). Conjugating WGA-HRP to nanoparticles may enable the creation of BBB-bypassing nanomedicine. Microfluidics and two-photon confocal microscopy is applied to screen nanocarriers for transport efficacy and gain mechanistic insights into their interactions with neurons. Protein modification of gold nanoparticles alters their cellular uptake at the axonal terminal and activates fast retrograde transport. Trajectory analysis of individual endosomes carrying the nanoparticles reveals a run-and-pause pattern along the axon with endosomes carrying WGA-HRP-conjugated gold nanoparticles exhibiting longer run duration and faster instantaneous velocity than those carrying nonconjugated nanoparticles. The results offer a mechanistic explanation of the different axonal transport dynamics as well as a cell-based functional assay of neuron-targeted nanoparticles with the goal of developing BBB-bypassing nanomedicine for the treatment of nervous system disorders.
Keyphrases
- gold nanoparticles
- blood brain barrier
- spinal cord injury
- cancer therapy
- photodynamic therapy
- drug delivery
- stem cells
- optic nerve
- protein protein
- walled carbon nanotubes
- single cell
- mass spectrometry
- nitric oxide
- cell therapy
- amino acid
- bone marrow
- combination therapy
- quantum dots
- optical coherence tomography
- smoking cessation
- tandem mass spectrometry
- peripheral nerve
- simultaneous determination