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. 2017 Nov 7;6:e31013. doi: 10.7554/eLife.31013

Figure 7. Reduced Ca2+-sensitivity of exocytosis in Otof C2C/C2C IHCs.

Figure 7.

(A) Mean ΔCm response curves (top) and normalized exocytosis rates (dCm/dt) (bottom), with mean intracellular fluorescent Ca2 signals of OGB-5N (green traces) recorded simultaneously after Ca2+ uncaging (purple arrowhead) in P14-P16 Otof C2C/+ (in black) and Otof C2C/C2C (in blue) IHCs. (B) Left: For each recorded Otof C2C/+ (in black) and Otof C2C/C2C (in blue) IHC, the rate of exocytosis was plotted as a function of [Ca2+]i, and each data set was fitted with a Hill function y = Vmax.x/(EC50+ xn). Right: Mean cooperativity and Ca2+-affinity of release in Otof C2C/+ and Otof C2C/C2C IHCs. Note that for 3 out of 6 Otof C2C/C2C IHCs, the fit of the sigmoidal Hill function to the data was only partial. For those IHCs, the Ca2+ affinity was estimated as the value of [Ca2+] for which dCm/dt = 0.5, rather than the EC50 of the fitted Hill function, which was larger. Data information: in (B), one IHC of each genotype was removed because of the lack of experimental points for a reliable fitting with a Hill function. In (A–B), data are presented as the mean ± SEM. **p<0.01, ns not significant (Mann-Whitney test).