Developmental changes in parvalbumin regulate presynaptic Ca2+ signaling

Certain interneurons contain large concentrations of specific Ca2+-binding proteins (CBPs), but consequences on presynaptic Ca2+ signaling are poorly understood. Here we show that expression of the slow CBP parvalbumin (PV) in cerebellar interneurons is cell specific and developmentally regulated, leading to characteristic changes in presynaptic Ca2+ dynamics (Ca-i). Using whole-cell recording and fluorescence imaging, we studied action potential-evoked Ca-i transients in axons of GABA-releasing interneurons from mouse cerebellum. At early developmental stages [postnatal days 10 - 12 (P10 - P12)], decay kinetics were significantly faster for basket cells than for stellate cells, whereas at P19 - P21 both interneurons displayed fast decay kinetics. Biochemical and immunocytochemical analysis showed parallel changes in the expression levels and cellular distribution of PV. By comparing wild-type and PV(-/-) mice, PV was shown to accelerate the initial decay of action potential-evoked Ca-i signals in single varicosities and to introduce an additional slow phase that summates during bursts of action potentials. The fast initial Ca-i decay accounts for a previous report that PV elimination favors synaptic facilitation. The slow decay component is responsible for a pronounced, PV-dependent, delayed transmitter release that we describe here at interneuron - interneuron synapses after presynaptic bursts of action potentials. Numerical simulations account for the effect of PV on Ca-i kinetics, allow estimates for the axonal PV concentration (similar to150 muM), and predict the time course of volume-averaged Ca-i in the absence of exogenous buffer. Overall, PV arises as a major contributor to presynaptic Ca-i signals and synaptic integration in the cerebellar cortex.