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Begin with an electrophysiology setup containing an immobilized transgenic fly with an exposed brain.
Position a recording micropipette near a postsynaptic neuron connected to a presynaptic neuron co-expressing tetrodotoxin-resistant sodium channels and red light-sensitive channels, and an interneuron with tetrodotoxin-sensitive sodium channels.
Apply mild suction to the micropipette to form a tight seal with the neuronal membrane.
Then, apply a strong suction to disrupt the membrane.
Maintain a constant cell potential. Introduce tetrodotoxin, which blocks sodium channels in the interneuron, preventing signal transmission from the interneuron to the postsynaptic neuron.
However, the tetrodotoxin-resistant sodium channels remain unaffected, allowing sodium ions to enter the presynaptic neuron.
Illuminate the fly with the red-light pulses.
This stimulates the light-sensitive channels, allowing cations to influx and activate the presynaptic neuron.
This presynaptic neuron directly transmits a signal to the postsynaptic neuron without involving the interneuron, and the resulting electrical activity confirms the monosynaptic connection.
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