MCU-mediated mitochondrial Ca2+ uptake does not modulate the photoresponses in Nckx1-/- mice. (A, B) Flash response families of dark adapted Nckx1-/- iCre+ (Nckx1-/- control; A) and Nckx1-/-Mcuf/f iCre+ double knockout (Nckx1-/- Rod Mcu-/-; B) mice from transretinal ERG recordings. Scotopic a-wave responses were recorded by a series of test flashes (1 ms in duration) with intensities (in photons/µm2) 1, 3.5, 10.2 (red traces), 35.4, 117. (C) Averaged rod responses (Mean ± SEM) from Nckx1-/- control (black; n = 10) and Nckx1-/- Rod Mcu-/- mice (red; n = 9) plotted as a function of flash intensity show a substantial reduction of the response amplitude in the double knockouts as compared to the controls. However, the sensitivity of the rods (estimated their normalized intensity response functions; Inset) remained unchanged between Nckx1-/- control (black) and Nckx1-/- Rod Mcu-/- (red) mice. (D) The kinetics of the dim flash response were not affected in the Nckx1-/- Rod Mcu-/- mice (n = 9); red trace) as compared to Nckx1-/- controls (n = 10; black trace).
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