LONG-TERM potentiation (LTP) is a cellular mechanism that potentially
underlies learning and memory(1). To test the hypothesis that LTP is i
nvolved in activity-dependent synapse formation, we combined whole-cel
l recordings and confocal microscopy to investigate hippocampal glutam
atergic synapses at their earliest stages of development. Here we repo
rt that, during the first postnatal week, the hippocampal glutamatergi
c network becomes gradually functional owing to the transformation of
precursor, pure NMDA (N-methyl-D-aspartate)-receptor-based synaptic co
ntacts into conducting AMPA -methylisoxazole-4-proprionate)/NMDA-recep
tor-type synapses. This functional synapse induction is caused by an a
ssociative form of LTP, so it is input-specific and easily triggered e
xperimentally by pairing presynaptic stimulation with postsynaptic dep
olarization. Our results challenge previous views that LTP occurs in t
he hippocampus only at later stages of development(2-6) and that its i
nduction requires dendritic spines(7). They also provide direct eviden
ce that LTP is important for the activity-dependent formation of condu
cting glutamatergic synapses in the developing mammalian brain.