Abstract
Axonal retrograde transport is essential for neuronal growth and survival. However, the nature and dynamics of the membrane compartments involved in this process are poorly characterized. To shed light on this pathway, we established an experimental system for the visualization and the quantitative study of retrograde transport in living motor neurons based on a fluorescent fragment of tetanus toxin (TeNT HC). Morphological and kinetic analysis of TeNT HC retrograde carriers reveals two major groups of organelles: round vesicles and fast tubular structures. TeNT HC carriers lack markers of the classical endocytic pathway and are not acidified during axonal transport. Importantly, TeNT HC and NGF share the same retrograde transport organelles, which are characterized by the presence of the neurotrophin receptor p75NTR. Our results provide the first direct visualization of retrograde transport in living motor neurons, and reveal a novel retrograde route that could be used both by physiological ligands (i.e., neurotrophins) and TeNT to enter the central nervous system.
MeSH Terms
Animals
Axonal Transport
Biological Transport
Cells, Cultured
Endocytosis
Lysosomes/metabolism
Microscopy, Fluorescence
Microscopy, Video
Motor Neurons/cytology,metabolism
Nerve Growth Factor/metabolism
Organelles/metabolism
Rats
Receptor, Nerve Growth Factor
Receptors, Nerve Growth Factor/metabolism
Tetanus Toxin/metabolism
Time Factors
Chemicals
Receptor, Nerve Growth Factor
Receptors, Nerve Growth Factor
Tetanus Toxin
Nerve Growth Factor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lalli Giovanna
Molecular NeuroPathoBiology Laboratory, Imperial Cancer Research Fund, London WC2A 3PX, United Kingdom.
Schiavo Giampietro
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