We next investigated whether there was a topographical organizati

We next investigated whether there was a topographical organization of unisensory responses in RL, and, if so, whether the two sensory maps were aligned. We used 3 × 4 grids of extracellular electrodes covering all of RL (see Experimental Procedures). For unimodal sensory input, we

separately stimulated the upper/lower and medial/lateral halves of both visual space and the whisker pad (Figure 1F). For each neuron, we computed a relative preference index as (U − L)/(U + L), where U and L are the neuronal responses to the upper or lower visual or tactile field stimulations, respectively. Then we averaged the relative spatial preference indexes of Selleck CP673451 all neurons along a given position of the grid. We finally mapped the spatial preference within RL for the upper versus lower and medial versus lateral stimulation for both modalities (Figure 1G). In line with (Marshel et al., 2011 and Wang and Burkhalter, 2007) we

found a retinotopic map within RL, but we also found a spatial segregation between responses elicited by the upper or lower aspects of the whisker pad. For example, the rostral part of RL preferentially responded to the upper visual field and to the upper whiskers. To quantify the degree of alignment between the two maps, we computed the correlation between the retinotopic and tactile maps along the same spatial direction (upper-lower and medial-lateral axes separately; Figure 1H). GSK1120212 order because We found a significant degree of spatial alignment of the somatic and visual spatial

preference maps along the upper-lower axis of the sensory space (black circles; r = 0.58, p < 0.001) but a weaker and nonsignificant alignment along its mediolateral axis (gray squares; r = 0.11, p = 0.44). We next compared bimodality and MI at the level of PSPs and of APs by IOI-targeted whole-cell recordings from layer 2/3 pyramids (n = 46 from 12 mice; Figure 2A). First, bimodal neurons were more abundant for PSPs (56% of responsive cells) compared to APs (39% of them; Figure 2B). Indeed, many neurons that were bimodal for PSPs were unimodal for APs (see example of Figure 2C): out of 24 neurons that were bimodal for PSPs, only 11 (46%) were bimodal for APs, 4 (17%) were unimodal and 9 did not respond with APs. Also, some cells with bimodal PSPs responded with APs only when V and T stimuli were simultaneously presented (multisensory—M stimulation; see example of Figure 2D). Second, we compared MI for PSPs and APs. Multisensory neurons display a response to a cross-modal combination of stimuli that is enhanced compared to the preferred unisensory stimulus (Stein and Stanford, 2008). To quantify such multisensory enhancement (ME), we computed an ME index, defined as (M−max(V,T))/max(V,T)(M−max(V,T))/max(V,T), where M is the response to M stimulation, and max(V,T) is the highest unimodal response.

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