(A) Intracellular responses of an RS_C neuron to repeated presentations (five) of a natural scene movie restricted to the classical receptive field (CRF). Average membrane potential (V_m) = −57.8 mV. Inset shows extent of the movie overlying the CRF; mask was opaque during recordings. The selectivity or sparseness index (S) was 0.29 ± 0.01 (mean and standard error of the mean [± SEM] throughout).
(B) Responses to five repeats of the same movie with a larger aperture that stimulated portions of the nonclas-sical receptive field (nCRF) in addition to the CRF. Average V_m = −65.7 mV. Sparseness increased to 0.72 ± 0.01. See also .
(C and D) Histograms of spiking responses to CRF stimulation (black) and (D) combined CRF + nCRF stimulation (red). Peak CRF response to best frame (45.9 Hz; black arrowhead) occurs 1.4 s after movie onset. Peak CRF + nCRF response (17.2 Hz; red arrowhead) occurs 0.6 s after movie onset. Histograms appear twice (C and D) and are overlaid to facilitate comparison. Note that CRF + nCRF costimulation results in the suppression of some peaks present in the CRF response (open arrows), while others are less affected (closed arrows). See also .
(E) Spiking responses became significantly more sparse (see text) in all 13 neurons (inset), corresponding to a 23% net increase in sparseness with combined CRF + nCRF stimulation (S_{CRF + nCRF} = 0.69 ± 0.02) compared with CRF alone stimulation (S_CRF = 0.56 ± 0.02; p < 0.01) across the population of RS_C neurons. See also .
(F) Neurons were significantly hyperpolarized (−1.6 mV on average; 10/13 individually, inset) during CRF + nCRF stimulation (V_{m CRF + nCRF} = −65.3 ± 0.4 mV; V_{m CRF} =−63.7 ± 0.6 mV; p < 0.01) in comparison to CRF only stimulation.

(A) Average inhibitory postsynaptic potentials (IPSPs) recorded during 12 presentations of a naturalistic movie to the CRF (black traces) and to the CRF + nCRF (blue). QX-314 and Cs⁺ in micropipette. Upper and lower thin traces indicate ± SEM. Dashed vertical line indicates movie onset, downward deflections indicate IPSPs. Some IPSP barrages increase greatly (closed arrows), while others change little (open arrows). CRF + nCRF stimulation significantly increases average IPSP amplitude (compared with average response during CRF stimulation) in this cell by −2.73 ± 0.51 mV (p < 0.01; recorded at 0 mV).
(B) In contrast to IPSPs, EPSPs (recorded at −75 mV) did not significantly differ in amplitude between the two conditions (−0.41 ± 0.61 mV; p > 0.1). The neuron shown here is the same neuron as shown in after spike inactivation.
(C) Population differences in EPSPs (red) and IPSPs (blue) evoked with CRF + nCRF stimulation, compared with CRF alone stimulation. All nine neurons were determined to be RS_C before spike inactivation. CRF + nCRF evoked IPSP barrages were significantly larger on average (blue, −1.99 ± 0.4 mV; 43.7 ± 12.0% increase; p < 0.01) while EPSP barrages were not (0.33 ± 0.2 mV; 4.9 ± 4.3% increase; p > 0.1). Values are mean ± SEM.

(A) Intracellular responses of an electrophysiologically identified FS interneuron (inset, shows sustained firing rate >300 Hz in response to current pulse) during ten trials of CRF stimulation (black).
(B) CRF + nCRF stimulation (red) elicits larger responses, compared with the CRF configuration (closed arrows).
(C) PSTHs from 15 repeated trials of CRF (black) and CRF + nCRF presentations (red) reveal elevated PSTH peaks (closed arrows), and the appearance of new peaks (open arrow) during wide-field stimulation. FS interneuron population (n = 5 intracellular, n = 4 extracellular) significantly decreased response sparseness (12%) with CRF + nCRF stimulation (S_CRF = 0.48 ± 0.007; S_{CRF + nCRF} = 0.43 ± 0.007; p < 0.01). Values are mean ± SEM.
(D) Intracellular response of an RS_TS neuron (inset, adapting firing pattern to current pulse, rate −100 Hz, spike width at half height 0.25 ms) during five trials of CRF stimulation (black).
(E) Response of same neuron to five trials of CRF + nCRF stimulation (red). Note increased action potential response (closed arrows) and addition of new responses (open arrow).
(F) PSTH across 15 trials of CRF stimulation (black) and CRF + nCRF stimulation (red) reveals elevated PSTH peaks (closed arrow), along with addition of peaks (open arrows) during wide-field stimulation. Inset, RS_TS neuron population (n = 12 intracellular, 3 juxtacellular) significantly decreased sparseness (7% average decrease; S_CRF = 0.66 ± 0.006; S_{CRF + nCRF} = 0.62 ± 0.005; p < 0.01) during CRF + nCRF stimulation. See for RS_TS neurons, and for biophysical and functional response properties of cell classes. Values are mean ± SEM.

(A) Response of an RS_C neuron to five natural movie presentations to the CRF (current pulse response, inset). Note the trial-to-trial variability of membrane potential (V_m) response.
(B) Same neuron, responses to five trials of CRF + nCRF movie. Across all 20 trials, there was a 21% increase in the reliability of V_m across trials (inset; R_Vm = 0.68) and a 163% increase in reliability of spike responses (R_Spikes = 0.29) compared with CRF stimulation (inset in 4A; R_Vm = 0.56; R_Spikes = 0.11; p < 0.01 for both comparisons). Sparseness across all trials also significantly increased (p < 0.01).
(C) Trial-to-trial membrane potential response reliability of RS_C neuron population (n = 13) significantly increases with CRF + nCRF stimulation (V_m R_CRF = 0.26 ± 0.01; V_m R_{CRF + nCRF} = 0.31 ± 0.01; p < 0.01) in parallel with increased reliability of spike responses in these same neurons (spikes R_CRF = 0.12 ± 0.01; spikes R_{CRF + nCRF} = 0.18 ± 0.01; p < 0.01). Values are mean ± SEM. See also for similar results in MU recordings.
(D) Isolated EPSPs significantly increase reliability (by 70%) with CRF + nCRF stimulation (EPSP R_CRF = 0.16 ± 0.01; EPSP R_{CRF + nCRF} = 0.27 ± 0.02; p < 0.01), while IPSP reliability does not significantly change (IPSP R_CRF = 0.14 ± 0.01; IPSP R_{CRF + nCRF} = 0.13 ± 0.01; p > 0.1).
(E) Normalized firing rates of both FS and RS_TS neurons increase significantly with CRF + nCRF stimulation (22.8 ± 6.3% and 26.8 ± 12.5%, respectively; p < 0.01, sign test), while normalized firing rates of RS_C neurons decrease significantly with CRF + nCRF stimulation (−21.2 ± 13.4%; p < 0.01, sign test). Firing rates normalized to CRF alone average firing rates for each neuron (FS: 7.6 ± 1.8 Hz; RS_TS: 2.8 ± 0.7 Hz; RS_C: 1.8 ± 1.2 Hz).
(F) RS_TS neurons significantly decrease their spike-train reliability (black and red, left) with CRF + nCRF stimulation, (R_CRF = 0.37 ± 0.02; R_{CRF + nCRF} = 0.30 ± 0.02; p < 0.01) while FS neurons maintain high spike-train reliability (black and blue, right) with CRF + nCRF stimulation, (R_CRF = 0.29 ± 0.02; R_{CRF + nCRF} = 0.28 ± 0.02; p > 0.1).

(A) Width of the autocovariance function of a representative RS_C neuron’s PSTH is significantly (35%) narrower with combined CRF + nCRF stimulation (red) compared with CRF alone stimulation (black). Across the population of RS_C neurons (n = 13), there was a significant narrowing (by 33%) of the average event in the PSTH with combined CRF + nCRF stimulation (181.6 ± 15.6 ms, red bar) compared with CRF alone stimulation (272.4 ± 23.9 ms, black bar; p < 0.01). See also for interspike interval histograms. Values are mean ± SEM.
(B) Spike-triggered average of V_m in these same neurons reveals a narrower synaptic potential underlying spikes, and more rapid prespike trajectory (from −179 ms to threshold) with CRF + nCRF stimulation compared with CRF alone stimulation (dV/dt _CRF = 0.062 ± 0.002 mV/ms; dV/dt _{CRF + nCRF} = 0.073 ± 0.002 mV/ms; p < 0.01). Traces aligned at spike threshold voltage before averaging (0 on ordinate). Inset shows that spike threshold is also significantly lower with wide-field stimulation (Threshold _{CRF + nCRF} = −55.1 ± 0.2 mV; Threshold _CRF = −54.2 ± 0.2 mV; p < 0.01). All data for n = 13 RS_C neurons (mean ± SEM).

(A) Correction for input resistance (R_in) and capacitance (C_m) of the recorded neuron allows inference of synaptic currents (IPSC or EPSC) that underlie an individual IPSP (left) or EPSP (right) amplitude-time series recorded in real neurons during CRF presentation. All traces in this figure were derived from data obtained from the neuron illustrated in and .
(B) Injection of these IPSC or EPSC traces into a leaky integrate and fire (LIF) model with experimentally measured R_in and C_m reproduces the original recorded IPSP (left) and EPSP (right) trace. Reconstructed example EPSP and IPSP amplitude-time series for CRF + nCRF stimulation shown in blue and red (lower traces).
(C) Excitatory and inhibitory conductances (G_e and G_i) derived from the reconstructed currents during CRF stimulation are injected into the LIF model cell at rest (−65 mV).
(D) Matrix of G_e and G_i combinations that can be examined in the LIF model. Injection of G_e and G_i from the same conditions (e.g., within CRF or CRF + nCRF stimulation) represents the control conditions (Da and Db). Mixing G_e and G_i obtained from different conditions represents our experimental manipulation (Dc and Dd).
(Ea) LIF raster and PSTH in response to 60 simulated (E + I)_CRF trials. Sparseness, S = 0.32 ± 0.002, spike-train reliability, R_CRF = 0.33 ± 0.02. (Eb) LIF raster and PSTH in response to 60 simulated (E + I)_{CRF + nCRF} trials. Sparseness and spike-train reliability increase significantly (S = 0.70 ± 0.002, spike train R_{CRF + nCRF} = 0.41 ± 0.02; p < 0.01 for both comparisons to CRF simulations). Note nonlinear change in shape of PSTH: some peaks are enhanced (solid arrowheads) while others are suppressed (open arrowhead). Correlation coefficient (r) of PSTH (E + I)_CRF to PSTH (E + I)_{CRF + nCRF} = 0.46 ± 0.02. (Ec) LIF raster and PSTH in response to 60 simulated (E_CRF + I_{CRF + nCRF}) trials. Sparseness increase significantly (S = 0.68 ± 0.002; p < 0.01) compared with (E + I)_CRF. Spike-train reliability decreased significantly in comparison to (E + I)_CRF simulations. (E_CRF + I_{CRF + nCRF}) R = 0.33 ± 0.02; p < 0.01. Correlation coefficient (r) of PSTH (E_CRF + I_{CRF + nCRF}) to PSTH (E + I)_{CRF + nCRF} = 0.47 ± 0.02. (Ed) LIF raster and PSTH in response to 60 simulated (E_{CRF + nCRF} + I_CRF) trials. Sparseness increased (S = 0.53 ± 0.002; p < 0.01), although significantly less than in (E_CRF + I_{CRF + nCRF}) simulation. However, spike-train reliability increased significantly in comparison to (E_CRF + I_{CRF + nCRF}) simulation (p < 0.01), and was not significantly different from (E + I)_CRF simulations, (E_{CRF + nCRF} + I_CRF) R = 0.40 ± 0.02; p > 0.1. Correlation coefficient of PSTH (E_{CRF + nCRF} + I_CRF) to PSTH (E + I)_{CRF + nCRF} = 0.97 ± 0.02, a significant (106%, p < 0.01) increase compared with (E_{CRF + nCRF} + I_CRF) simulations.

(A) LIF simulations derived from population of real neurons (n = 9; see ) indicate that spike-train sparseness was significantly lower in the (E + I)_{CRF + nCRF} simulations compared with the three other simulation conditions (S = 0.47 ± 0.04; colored asterisks indicate significant group differences corrected for multiple comparisons). Response sparseness in the E_CRF + I_{CRF + nCRF} simulations (blue; S = 0.65 ± 0.04) was not significantly different than the (E + I)_{CRF + nCRF} simulation (violet; S = 0.65 ± 0.03; p > 0.1), but both of these groups displayed significantly larger response sparseness than the E_{CRF + nCRF} + I_CRF simulations (red; S = 0.58 ± 0.03; p < 0.01 for both group comparisons). Colored asterisks indicate significant group differences. Values are mean ± SEM.
(B) Conversely, trial-to-trial spike-train reliability is highest for the (E + I)_{CRF + nCRF} simulations (violet; R = 0.2 ± 0.007), and these spike trains were not significantly more reliable than those in the E_{CRF + nCRF} + I_CRF simulations (red; R = 0.19 ± 0.007; p > 0.1). However, spike responses of both of these groups were significantly more reliable than the spike trains of the E_CRF + I_{CRF + nCRF} simulations (blue; R = 0.17 ± 0.006; p < 0.01 for both group comparisons).
(C) Summary of LIF simulations shows that overall spiking pattern (PSTH) of E_{CRF + nCRF} + I_CRF simulations is the most similar to (E + I)_{CRF + nCRF} PSTH (red; r = 0.74 ± 0.007), although the E_CRF + I_{CRF + nCRF} PSTH was significantly more similar to the (E + I)_{CRF + nCRF} PSTH (blue; r = 0.46 ± 0.008), as compared with the similarity of the (E + I)_CRF PSTH to the (E + I)_{CRF + nCRF} PSTH (black; r = 0.26 ± 0.007; p < 0.01 for all group comparisons). See also for effects of manipulating timing of G_i relative to G_e.

(A) Local cortical networks composed of excitatory (white) and inhibitory (black) neurons form interconnections with each other, with the great majority of connectivity occurring among excitatory neurons. During CRF stimulation, both excitatory and inhibitory cell types are driven, with RS_C neurons and FS neurons generating elevated and temporally varying responses (traces).
(B) Upon simultaneous engagement of the CRF and nCRF, inhibitory interneurons become strongly activated by increased excitatory drive arising from a larger spatial distribution of inputs. The increased depolarization and enhanced synaptic fluctuations in interneurons are nonlinearly transformed into greater numbers of spikes compared with excitatory neurons (inset at center). This causes RS_C neurons to receive enhanced inhibitory synaptic barrages at specific time points, which leads to increased sparseness and precision of visually evoked spike responses in RS_C neurons. These sparser but less variable spikes are amplified through the recurrent excitatory connections among RS_C neurons in the local network (red synapse), which leads to more reliable and precise sensory encoding across the ensemble of pyramidal neurons (red trace).