Confocal laser scanning microscopy reveals voltage‐gated calcium signals within hippocampal dendritic spines

Abstract

The induction of long‐term potentiation (LTP) is generally assumed to be triggered by Ca²⁺ entry into dendritic spines via NMDA receptor‐gated channels. A previous computational model proposed that spines serve several functions in this process. First, they compartmentalize and amplify increases in [Ca²⁺]_i. Second, they augment the nonlinear relationship between synaptic strength and the probability or magnitude of LTP induction. Third, they isolate the metabolic machinery responsible for LTP induction from increases in [Ca²⁺]_i produced by voltage‐gated Ca²⁺ channels in the dendritic shaft. Here we examine this last prediction of the model using methods that combine confocal microscopy with simultaneous neurophysiological recordings in hippocampal brain slices. Either of two Ca²⁺‐sensitive dyes were injected into CA1 pyramidal neurons. Direct depolarization of the neurons via the somatic electrode produced clear increases in Ca²⁺ signals within the dendritic spines, a result that was not predicted by the previous spine model. Our new spine model suggests that some of this signal could theoretically result from Ca²⁺‐bound dye diffusing from the dendritic shaft into the spine. Dye diffusion alone cannot, however, explain the numerous cases in which the Ca²⁺ signal in the spine was considerably larger than that in the adjacent dendritic shaft. The latter observations raise the possiblity of voltage‐gated Ca²⁺ entry directly into the spine or else perhaps via Ca²⁺‐dependent Ca²⁺release. The new spine model accommodates these observations as well as several other recent experimental results. 1994 John Wiley & Sons, Inc.