Ever since their first description in neurons, dendritic spines could
be visualized only in fixed tissue, using high-power light and electro
n microscopy. Recent studies have been able to measure the free intrac
ellular Ca2+ concentration ([Ca2+](i)) in dendritic spines of live neu
rons, and the results suggest that the spine is an independent cellula
r Ca2+ compartment, Other recent observations have indicated that the
density of spines on dendrites changes in a dynamic fashion depending
on ongoing neuronal activity. Together, these findings have led to the
proposal that the dendritic spine is not only a storage device for lo
ng-term memory but perhaps a means for isolating the cell from the har
mful consequences of synaptically evoked surges in [Ca2+](i). In other
words, the dendritic spine is a neuroprotectant. This hypothesis has
specific testable implications, including relating cell activity to sp
ine density.