The effects of progressive neural tissue degeneration can be imitated by administering compounds based on neuro-toxic viral proteins to neuron cultures. The toxins cause oxidative stress damage and free radical production, and will trigger apoptotic cell death in the neurons.
The capability and the power of a given therapeutic agent in reducing the effects of degeneration and death of neuronal tissue can be quantified by screening the health status of the neuron cultures, previously treated with toxins, after the administration of such therapeutic agent. Further, it can be evaluated whether the therapeutic agent has axo-dendritic protective effect, meaning the capability to minimize pruning of axons and dendrites for every neuron.
The images here were acquired with fluorescence microscopy, and the cell cultures are from rat mixed hippocampal cultures which were transfected with a neuron-specific promoter containing the red fluorescent protein tdTomato, with Tau fusion protein linked to the tdTomato. These have been generated with double transfection-yellow making the neurites appear in green, while the cell bodies appear red. Toxins, along with a therapeutic agent are added to the culture to study the effect on the cell body number and process length.
Rat, Cell Body Number and Neurite Length
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