Glutamatergic synapses vary, exhibiting EPSCs of widely different magnitude
s and timecourses. The main contributors to this variability are: presynapt
ic factors, including release probability, quantal content and vesicle comp
osition; factors that modulate the concentration and longevity of glutamate
in the cleft, including diffusion and the actions of glutamate transporter
s; and postsynaptic factors, including the types and locations of ionotropi
c glutamate receptors, their numbers, and the nature and locations of assoc
iated intracellular signalling systems.