In the scientific quest to
unravel the neural basis of many perceptual and cognitive functions, animal
models are very important in complementing the findings obtained in
non-invasive human neuroimaging studies. Furthermore, even though there are
many species-specific aspects to cognition (e.g.,
human language), for those perceptual-cognitive functions that do generalize
across species, animal models often offer the only possibility to test
decisively between alternative hypotheses. Further, development of animal
research methods is advancing at astounding speed. Two-photon calcium imaging
is a relatively new method that allows simultaneous recording from large (~hundreds)
populations of neurons, however, the method has been limited to recording from
limited number of cortical layers at a time, and it has not been possible to
record the neural populations over extended periods of time, which would be
very useful in studies of, for example, the neural basis of various types of
learning.
With the method recently
published by Andermann et al. (2013) it
is now possible to record extensive populations of neurons simultaneously from
all six cortical layers over extended periods of time, even for months. The
authors surgically implanted glass microprisms in somatosensory and visual
cortical areas of mice, which then allowed chronic two-photon imaging of
hundreds of neurons and from all layers simultaneously, in awake animals. The
authors point out that their novel methodology, when combined with advances in
genetic, pharmacological, and optogenetic methods (using which individual
neurons in a population can be selectively suppressed and excited), can
considerably expand the highly exciting capabilities offered by two-photon
imaging in animal-model studies of the neural basis of perceptual and cognitive
functions.
Reference: Andermann ML, Gilfoy NB, Goldey GJ, Sachdev RNS, Wölfel
M, McGormick DA, Reid RC, Levene MJ. Chronic cellular imaging of entire
cortical columns in awake mice using microprisms. Neuron (2013) e-publication
ahead of print. http://dx.doi.org/10.1016/j.neuron.2013.07.052
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