Calcium imaging in vivo

Caged compounds

Dual 2-photon microscope


 

Calcium Imaging In Vivo

Astrocytes are not only the “glue’ that hold neurons together, providing nutrients for their function, but they are also now seen as important modulators of synaptic activity. They have come to be seen as key partners in what is called the “tripartite synapse” (i.e. 1. presynaptic terminals, 2. postsynaptic terminals, and 3. the surrounding astrocytes). Increases in astrocytic Ca releases glutamate and ATP onto neurons, modulating and integrating neuronal excitability.

Mapping of nicotinic acetylcholine receptor (nAChR) subtypes and subunits in human brain is far from complete, however it is clear that multiple subunits are present (including alpha3, alpha4, alpha5, alpha6 and alpha7, beta2, alpha3 and beta4) and that these receptors are not solely distributed on neurons, but also on cerebral vasculature and astrocytes. Changes in nAChR expression in neuropsychiatric disorders appear to be brain region and subtype specific and have been shown in some instances to be associated with pathology and symptomatology. The lab uses 2-photon microscopy (2PM) to study cortical astrocytic calcium signaling in vivo in normal and diseased states.

(Image of layer 1 and 2/3 cortical astrocytes in a living mouse taken on our 2P microscope.)

 


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