Fluctuation analysis in nonstationary conditions: single Ca channel current in cortical pyramidal neurons

TL;DR

This study introduces a robust fluctuation analysis method to measure single Ca2+ channel currents in cortical neurons under nonstationary conditions, providing insights into calcium signaling and channel properties.

Contribution

Developed a new fluctuation analysis technique using mean current fitting and band-pass filtering for accurate measurement of VGCC currents during rundown.

Findings

Single channel current amplitude is about 0.04 pA at 1 mM Ca2+

Current amplitude increases with external Ca2+ concentration

Relaxation time constant of fluctuations is 0.2-0.8 ms

Abstract

Fluctuation analysis is a method which allows measurement of the single channel current of ion channels even when it is too small to be resolved directly with the patch clamp technique. This is the case for voltage-gated Ca2+ channels (VGCCs). They are present in all mammalian central neurons, controlling presynaptic release of transmitter, postsynaptic signaling and synaptic integration. The amplitudes of their single channel currents in a physiological concentration of extracellular Ca2+, however, are small and not well determined. But measurement of this quantity is essential for estimating numbers of functional VGCCs in the membrane and the size of channel-associated Ca2+ signaling domains, and for understanding the stochastic nature of Ca2+ signaling. Here, we recorded the VGCC current in nucleated patches from layer 5 pyramidal neurons in rat neocortex, in physiological external Ca2+ (1-2 mM). The ensemble-averaging of current responses required for conventional fluctuation analysis proved impractical because of the rapid rundown of VGCC currents. We therefore developed a more robust method, using mean current fitting of individual current responses and band-pass filtering. Furthermore, voltage ramp stimulation proved useful. We validated the accuracy of the method by analyzing simulated data. At an external Ca2+ concentration of 1 mM, and a membrane potential of -20 mV, we found that the average single channel current amplitude was about 0.04 pA, increasing to 0.065 pA at 2 mM external Ca2+, and 0.12 pA at 5 mM. The relaxation time constant of the fluctuations was in the range 0.2-0.8 ms. The results are relevant to understanding the stochastic properties of dendritic Ca2+ spikes in neocortical layer 5 pyramidal neurons. With the reported method, single channel current amplitude of native VGCCs can be resolved accurately despite conditions of unstable rundown.