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. Author manuscript; available in PMC: 2017 Apr 1.
Published in final edited form as: Trends Cell Biol. 2016 Feb 16;26(4):300–312. doi: 10.1016/j.tcb.2016.01.003

Figure 3. Ca2+ signals in hippocampal astrocytes from wild type and Ip3r2–/– mice.

Figure 3

(A) Schematic illustrating the experimental approach. AAVs were microinjected in vivo, brain slices were imaged ∼ 2 weeks later and Ca2+ signals analyzed in a semi automated manner using custom software called GECIquant. (B) Representative images and traces for Ca2+ signals measured in an astrocyte from a WT mouse. Three predominant types of Ca2+ signal are demarcated: somatic signals (green), waves (red) and microdomains (yellow). Approximate territory boundaries are outlined in blue. (C) As in B, but for two astrocytes from an Ip3r2–/– mouse; somatic signals are largely absent, but many signals persist in branches. Figure from a recent paper [38].

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