Glutamate-Bound NMDARs Arising from In Vivo-like Network Activity Extend Spatio-temporal Integration in a L5 Cortical Pyramidal Cell Model
Figure 8
Background excitatory input lowers threshold, extends duration and regeneration of NMDAR spikes in a passive model.
(A) Probability of triggering an NMDAR spike (P(NMDAR spike)) in terminal branches versus number of nearly synchronous stimulated synapses in a passive model (solid lines), where all non-synaptic active dendritic conductances have been removed, in the absence (black) and presence of 1500 background excitatory synapses (blue). Original model shown for comparison (dashed lines). (B) NMDAR spike decay time distribution (N = 100, triggered with 30 synapses each) lines as for (A). Excitatory decay times distribution during control and during background activity. Inset, mean voltage (±SD) in randomly selected terminal branches (N = 100) with and without background activity in passive (filled symbols) and original model (open symbols). (C) Membrane voltage traces from all 28 terminal apical branches (as in Fig. 7) in the passive model for a single trial, during nearly synchoronous activation of branch 11 (red traces) in the presence (upper trace; blue) and absence (lower trace; black) of background activity from 1500 excitatory inputs. Linear sum of the depolarization during control and during background input only, shown in green. (D) Peak depolarization induced by an NMDAR spike in branch 11 versus terminal branch number in absence (black) and presence (blue) of background activity. Peak depolarization during background activity alone shown in grey and peak value of linear sum of control during stimulation of branch 11 and background-only shown in green. (E) Voltage traces from branch 11 (red) and branch 7 (blue) in the absence (dashed lines) and presence of 1500 background excitatory inputs (solid lines). Grey and green trace as in (D). (F) Number of additional branches activated during background input when a single branch is stimulated (empty bar). This was estimated by stimulating the terminal branches in turn for 10 trials each and applying the 13 mV criterion, which identified regenerative peaks, although the number of branches exhibiting regenerative events is probably overestimated due to passive spread of voltage. Solid bar shows original model for comparison.