Inverted Encoding Models Assay Population-Level Stimulus Representations, Not Single-Unit Neural Tuning

Thomas C Sprague, Kirsten C S Adam, Joshua J Foster, Masih Rahmati, David W Sutterer, Vy A Vo, Thomas C Sprague, Kirsten C S Adam, Joshua J Foster, Masih Rahmati, David W Sutterer, Vy A Vo

No abstract available

Keywords: cognitive vision; computational neuroimaging; fMRI; inverted encoding model.

Figures

Figure 1.
Figure 1.
IEM: use neural tuning as an assumption to estimate population-level representations. A, The IEM framework assumes that aggregate neural responses (e.g., voxels) can be modeled as a combination of feature-selective information channels (i.e., orientation-selective neural populations). Tuning properties of modeled information channels are experimenter defined and often based on findings in the single-unit physiology literature. B, Once an encoding model (A) is defined, it can be used to predict how each information channel should respond to each stimulus in the experiment. These predicted channel responses are used to fit the encoding model to each voxel’s activation across all trials in a “training” dataset, often balanced across experimental conditions, or derived from a separate “localizer” or “mapping” task. C, By inverting the encoding models estimated across all voxels (typically, within an independently-defined region), new activation patterns can be used to compute the response of each modeled neural information channel. This step transforms activation patterns from measurement space (one number per measurement dimension, e.g., voxel) to information space (one number per modeled information channel, A). These computed channel response functions can be aligned based on the known stimulus feature value on each trial (black arrowheads), and quantified and compared across conditions (e.g., manipulations of stimulus contrast, spatial attention, etc.), especially when a fixed encoding model is used for reconstruction (as schematized here). Cartoon data shown throughout figure.

References

    1. Brouwer G, Heeger D (2011) Cross-orientation suppression in human visual cortex. J Neurophysiol 106:2108–2119. 10.1152/jn.00540.2011
    1. Brouwer G, Heeger D (2009) Decoding and reconstructing color from responses in human visual cortex. J Neurosci 29:13992–14003. 10.1523/JNEUROSCI.3577-09.2009
    1. Brouwer GJ, Heeger DJ (2013) Categorical clustering of the neural representation of color. J Neurosci 33:15454–15465. 10.1523/JNEUROSCI.2472-13.2013
    1. Churchland PS, Sejnowski TJ (1988) Perspectives on cognitive neuroscience. Science 242:741–745.
    1. Dumoulin S, Wandell B (2008) Population receptive field estimates in human visual cortex. Neuroimage 39:647–660. 10.1016/j.neuroimage.2007.09.034
    1. Foster JJ, Sutterer DW, Serences JT, Vogel EK, Awh E (2017) Alpha-band oscillations enable spatially and temporally resolved tracking of covert spatial attention. Psychol Sci 28:929–941. 10.1177/0956797617699167
    1. Garcia J, Srinivasan R, Serences J (2013) Near-real-time feature-selective modulations in human cortex. Curr Biol 23:515–522. 10.1016/j.cub.2013.02.013
    1. Graf ABA, Kohn A, Jazayeri M, Movshon JA (2011) Decoding the activity of neuronal populations in macaque primary visual cortex. Nat Neurosci 14:239–245. 10.1038/nn.2733
    1. Jazayeri M, Movshon JA (2006) Optimal representation of sensory information by neural populations. Nat Neurosci 9:690–696. 10.1038/nn1691
    1. Kay KN, Weiner KS, Grill-Spector K (2015) Attention reduces spatial uncertainty in human ventral temporal cortex. Curr Biol 25:595–600.
    1. Klein BP, Harvey BM, Dumoulin SO (2014) Attraction of position preference by spatial attention throughout human visual cortex. Neuron 84:227–237. 10.1016/j.neuron.2014.08.047
    1. Kok P, Mostert P, de Lange FP (2017) Prior expectations induce prestimulus sensory templates. Proc Natl Acad Sci USA 114:10473–10478. 10.1073/pnas.1705652114
    1. Liu T, Cable D, Gardner JL (2018) Inverted encoding models of human population response conflate noise and neural tuning width. J Neurosci 38:398–408. 10.1523/JNEUROSCI.2453-17.2017
    1. Ma WJ, Beck JM, Latham PE, Pouget A (2006) Bayesian inference with probabilistic population codes. Nat Neurosci 9:1432–1438. 10.1038/nn1790
    1. Myers NE, Rohenkohl G, Wyart V, Woolrich MW, Nobre AC, Stokes MG (2015) Testing sensory evidence against mnemonic templates. Elife 4:e09000. 10.7554/eLife.09000
    1. Rahmati M, Saber GT, Curtis CE (2018) Population dynamics of early visual cortex during working memory. J Cogn Neurosci 30:219–233. 10.1162/jocn_a_01196
    1. Sclar G, Freeman RD (1982) Orientation selectivity in the cat’s striate cortex is invariant with stimulus contrast. Exp Brain Res 46:457–461. 10.1007/BF00238641
    1. Scolari M, Byers A, Serences JT (2012) Optimal deployment of attentional gain during fine discriminations. J Neurosci 32:1–11. 10.1523/JNEUROSCI.5558-11.2012
    1. Sheremata SL, Silver MA (2015) Hemisphere-dependent attentional modulation of human parietal visual field representations. J Neurosci 35:508–517. 10.1523/JNEUROSCI.2378-14.2015
    1. Sprague TC, Serences JT (2013) Attention modulates spatial priority maps in the human occipital, parietal and frontal cortices. Nat Neurosci 16:1879–1887. 10.1038/nn.3574
    1. Sprague TC, Saproo S, Serences JT (2015) Visual attention mitigates information loss in small- and large-scale neural codes. Trends Cogn Sci 19:215–226. 10.1016/j.tics.2015.02.005
    1. Sprague TC, Ester EF, Serences JT (2016) Restoring latent visual working memory representations in human cortex. Neuron 91:694–707. 10.1016/j.neuron.2016.07.006
    1. Sprague TC, Itthipuripat S, Vo VA, Serences JT (2018) Dissociable signatures of visual salience and behavioral relevance across attentional priority maps in human cortex. J Neurophysiol. Advance online publication. Retrieved May 16, 2018 10.1152/jn.00059.2018
    1. Vo VA, Sprague TC, Serences JT (2017) Spatial tuning shifts increase the discriminability and fidelity of population codes in visual cortex. J Neurosci 37:3386–3401. 10.1523/JNEUROSCI.3484-16.2017
    1. Wandell BA, Winawer J (2015) Computational neuroimaging and population receptive fields. Trends Cogn Sci 19:349–357. 10.1016/j.tics.2015.03.009

Source: PubMed

3
Sottoscrivi