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. Author manuscript; available in PMC: 2019 Jul 21.
Published in final edited form as: Cell Rep. 2018 Apr 17;23(3):878–887. doi: 10.1016/j.celrep.2018.03.095

Figure 4. SF Axon Terminal Activity Is Increased in cyfip2 Mutants.

Figure 4.

(A) Maximum intensity projection of Tg(−6.7FRhcrtR:gal4VP16); Tg(UAS:GCaMP5), showing labeled SF neurons (green). M-cells (M) and other reticulospinal neurons were labeled with rhodamine dextran (magenta). Arrowheads indicate SF cell bodies, and asterisks mark SF axon terminals in the M-cell axon cap. Scale bar, 10 μm.

(B) Representative pseudocolored images of baseline (F0) and peak fluorescence in SF axon terminals following a strong acoustic stimulus (13 dB; the color scale denotes fluorescence intensity; black, lowest; white, highest). Scale bar, 10 μm.

(C) Averaged traces of SF terminal Ca2+ responses following low (−14 dB), medium (−12 dB), and strong (13 dB) acoustic stimuli (n = 42 responses from 10 siblings, blue line; n = 36 responses from 9 mutants, red line; mean ± SEM; *p < 0.05, Mann-Whitney test).

(D) Scatterplot of the area under the curve for individual SF axon terminal Ca2+ responses (mean ± SD; **p = 0.0049, ***p = 0.0003, Mann-Whitney test).