Abstract
Background: The rate-limiting step that determines the dominant time constant (τD) of mammalian rod photoresponse recovery is the deactivation of the active phosphodiesterase (PDE6). Physiologically relevant Ca2+-dependent mechanisms that would affect the PDE inactivation have not been identified. However, recently it has been shown that τD is modulated by background light in mouse rods. Methodology/Principal Findings: We used ex vivo ERG technique to record pharmacologically isolated photoreceptor responses (fast PIII component). We show a novel static effect of calcium on mouse rod phototransduction: Ca2+ shortens the dominant time constant (τD) of saturated photoresponse recovery, i.e., when extracellular free Ca2+ is decreased from 1 mM to ~ 25 nM, the τD is reversibly increased ~1.5-2-fold. Conclusions: We conclude that the increase in τD during low Ca2+ treatment is not due to increased [cGMP], increased [Na+] or decreased [ATP] in rod outer segment (ROS). Also it cannot be due to protein translocation mechanisms. We suggest that a Ca2+-dependent mechanism controls the life time of active PDE. © 2010 Vinberg, Koskelainen.
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CITATION STYLE
Vinberg, F., & Koskelainen, A. (2010). Calcium sets the physiological value of the dominant time constant of saturated mouse rod photoresponse recovery. PLoS ONE, 5(9). https://doi.org/10.1371/journal.pone.0013025
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