MORPHOLOGICALLY a synapse consists of a presynaptic release site conta
ining vesicles, a postsynaptic element with membrane specialization, a
nd a synaptic cleft between them1. The number of release sites shapes
the properties of synaptic transmission between neurons2-4. Although e
xcitatory interactions between cortical neurons have been examined5-9,
the number of release sites remains unknown. We have now recorded exc
itatory postsynaptic potentials evoked by single pyramidal cells in hi
ppocampal interneurons and visualized both cells using biocytin inject
ions. Light and electron microscopy showed that excitatory postsynapti
c potentials were mediated by a single synapse. We also reconstructed
the entire axon arborization of single pyramidal cells, filled in vivo
, in sections counterstained for parvalbumin, which selectively marks
basket and axo-axonic cells10,11. Single synaptic contacts between pyr
amidal cells and parvalbumin-containing neurons were dominant (>80%),
providing evidence for high convergence and divergence in hippocampal
networks12.