GEORGE RETSECK; NEURON IMAGE COURTESY OF QIAN CHEN AND GUOPING FENG
Observing the activity of specific neuronal circuits in the living brain can provide insight into how the brain functions normally and how it is affected by disease, psychological disorder, or injury. For that purpose, Guoping Feng, from the Massachusetts Institute of Technology, and colleagues have engineered transgenic mice whose neurons glow green when activated.
Neuronal activation leads to a rapid spike in intracellular calcium—a fact that prompted the development of fluorescent calcium dyes. But while these dyes provide an excellent readout of neuronal activity, says Feng, “you cannot put dyes into a specific population of neurons. . . . [And] you cannot image the same neurons over a long period of time.”
To get around these shortcomings, researchers have developed genetically encoded calcium indicators such as GCaMP—a calcium-binding peptide linked to a green fluorescent protein. “There has been an evolution of the technique, in which people have made brighter and brighter genetically encoded reporters and found various ways to insert them in vivo—viral vectors, transgenes, etc.,” says Joshua Sanes of Harvard University, who was not involved in the new study.
Feng and colleagues have come up with “another good tool,” says Sanes. They’ve created two transgenic mouse lines that express GCaMP2.2c and GCaMP3—improved, brighter versions of GCaMP—specifically in selected types of neurons. These mice enable the observation of both spontaneous neural network activation—in awake but unstimulated animals—and stimuli-induced activation.
Sanes, who studies vision, plans to use Feng’s mice to look for patterns of neuronal activity in response to visual stimuli. Feng, meanwhile, plans to cross the mice with mouse models of autism and obsessive-compulsive disorder to see how neuronal pathways are affected in these conditions. (Neuron, 76:297-308, 2012)
|MICE FOR OBSERVING NEURONAL ACTIVITY||REFERENCE||HOW IT WORKS||FEATURES||AVAILABLE FROM|
| Cre-inducible |
| J Neurosci, 32:3131-41, 2012 || Expression of GCaMP3 depends on presence of the DNA recombinase Cre. Crossing GCaMP3 mice with mice expressing Cre in specific neurons enables the expression of GCaMP3 in neurons. ||Any specific type of neuron could be targeted if an appropriate Cre-expressing line is available.|| The Jackson Laboratory |
Stock no. 014538
|Thy1-controlled GCaMP2.2c and GCaMP3 mice|| Neuron, |
|Thy1 is a neuronal specific and drives the expression of the GCaMP derivatives.||Good for monitoring neuronal activation over large regions of the brain.|| The Jackson Laboratory |
Stock nos. 017892 (GCaMP2.2) and 017893 (GCaMP3)