In brains that learn with ease, groups
of nerve cells switch easily between conversations with other cells in their networks.
Not exact matches
Duke University biologist Pelin Volkan and colleagues have identified a set
of genetic control
switches that interact early in a fly's development to generate dozens
of types
of olfactory neurons, specialized
nerve cells for smell.
The
switch works by regulating the activity
of a handful
of sleep - promoting
nerve cells, or neurons, in the brain.
Measurements
of the electrical activity
of nerve cells in two key areas
of the brain showed a surprising result:
nerve cells in the prefrontal cortex signaled the distraction while it was being presented, but immediately restored the remembered information (the number
of dots) once the distraction was
switched off.
In a brain slice, Olivia Masseck measures the activity
of nerve cells in which she
switches on their receptors using light stimulation.
The work is part
of a growing field called optogenetics, and used light - activated proteins from photosynthetic algae to
switch nerve cells on and off.
The researchers inserted an optogenetic
switch into a group
of nerve cells located in the ancient part
of the brain called the medulla, allowing them to activate or inactivate the neurons with laser light.
Instead
of issuing orders to make mature macrophages
switch roles, they filled the
nerve bridge with a biological signal shown to attract younger, undifferentiated
cells destined to become pro-healing macrophages.
Now, Professor Martin and colleagues have discovered that in response to specific types
of cell damage, Parkin can trigger the self - destruction
of «injured»
nerve cells by
switching on a controlled process
of «cellular suicide» called apoptosis.
For example, Bonin explains, a study might test whether turning on two types
of nerve cells — each with a different opsin — gives different results from
switching on just one.
Nerve - signaling chemicals called neurotransmitters can «
switch off» or dampen the activity
of cells that signal arousal or relaxation.