Interacting intracellular signalling pathways can perform computations
on a scale that is slower, but more fine-grained, than the interactio
ns between neurons upon which we normally build our computational mode
ls of the brain (Bray D 1995 Nature 376 307-12). What computations mig
ht these potentially powerful intraneuronal mechanisms be performing?
The answer suggested here is: storage of spatio temporal sequences of
synaptic excitation so that each individual neuron can recognize recur
rent patterns that have excited it in the past. The experimental facts
about directionally selective neurons in the visual system show that
neurons do not integrate separately in space and time, but along strai
ght spatio-temporal trajectories; thus, neurons have some of the capac
ities required to perform such a task. In the retina, it is suggested
that calcium-induced calcium release (CICR) may provide the basis for
directional selectivity. In the cortex, if activation mechanisms with
different delays could be separately reinforced at individual synapses
, then each such Hebbian super-synapse would store a memory trace of t
he delay between pre- and post-synaptic activity, forming an ideal bas
is for the memory and response to phase sequences.