Patching a Purkinje neuron

Patching a Purkinje neuron

Patching Neurons

I create my neuron art images by using an extremely delicate technique called patch-clamp electrophysiology in combination with calcium imaging.  In simpler terms, what I do is connect a small glass tube (pipette) to the round part of the neuron (the cell body or soma), and I flow fluorescent dye through the tube into the cell like how gasoline flows into a gas tank.  Over 40 minutes, the dye spreads through all the small branches of the neuron.

 A dendrite filled with green fluorescent dye

A dendrite filled with green fluorescent dye

Calcium Ions + autism

As the fluorescent dye flows into the cell, it binds with calcium ions that are already inside the neuron.  I shock the neuron with a mild spurt of electricity, which causes the calcium to move, and the dye moves with it.  Calcium movement correlates with activity in the neuron, so with these experiments, my goal is to look at how the dye moves through these neurons in an autistic cerebellum vs. a non-autistic cerebellum.  By comparing these, I am able to study what is different about the autistic brain.  Learn more about my autism research here.

 Me, performing experiments at the microscope in the Hansel Lab at The University of Chicago

Me, performing experiments at the microscope in the Hansel Lab at The University of Chicago

3d laser imaging

At the end of the experiment, I use a confocal microscope to collect a three-dimensional image of the neuron.  I create these images by shining lasers on the fluorescent dye.  Often, I add extra background lighting to create additional colors or stripes that show off the texture of the brain slice.  It takes about 20 minutes to scan the ~100 micron (0.1 millimeter) length of the neuron in three dimensions.  When the microscope is done, I make a few adjustments, et voilà: neuron art!