scholarly journals Learning enhances sensory processing in mouse V1 before improving behavior

2016 ◽  
Author(s):  
Ovidiu Jurjut ◽  
Petya Georgieva ◽  
Laura Busse ◽  
Steffen Katzner

AbstractA fundamental property of visual cortex is to enhance the representation of those stimuli that are relevant for behavior, but it remains poorly understood how such enhanced representations arise during learning. Using classical conditioning in mice, we show that orientation discrimination is learned in a sequence of distinct behavioral stages, in which animals first rely on stimulus appearance before exploiting its orientation to guide behavior. After confirming that orientation discrimination under classical conditioning requires primary visual cortex (V1), we measured, during learning, response properties of V1 neurons. Learning improved neural discriminability, sharpened orientation tuning and led to higher contrast sensitivity. Remarkably, these learning-related improvements in the V1 representation were fully expressed before successful orientation discrimination was evident in the animals’ behavior. We propose that V1 plays a key role early in discrimination learning to enhance behaviorally relevant sensory information.

2021 ◽  
Author(s):  
Marc M. Himmelberg ◽  
Jonathan Winawer ◽  
Marisa Carrasco

ABSTRACTThe size and organization of primary visual cortex (V1) varies across individuals. Across neurotypical adults, V1 size varies more than twofold. Within individuals, surface area per unit of visual field – cortical magnification – varies with eccentricity and polar angle. Contrast sensitivity and cortical magnification covary with eccentricity, therefore it has been hypothesized that cortical magnification, specifically the number of activated V1 neurons, limits contrast sensitivity. Here, we quantify the relation between contrast sensitivity and V1 cortical magnification across observers and polar angle. We measured contrast sensitivity at four cardinal meridians in 29 observers. We then used fMRI to measure the size of V1 in the same observers, and the amount of surface area representing each of the four meridians (wedge-ROIs within 15° polar angle of the meridians, 1 to 8° eccentricity). We found that: First, an observer’s contrast sensitivity (averaged across polar angles) was predicted by the size of V1. Second, contrast sensitivity at each cardinal meridian was correlated with the surface area of the wedge-ROIs centered at the corresponding meridian. Third, increases in contrast sensitivity and cortical magnification at the horizontal compared to vertical meridian (horizontal-vertical anisotropy, ‘HVA’) were strongly correlated: a larger HVA in contrast sensitivity corresponded to a larger HVA in cortical magnification. These results reveal that contrast sensitivity and cortical magnification co-vary across observers and demonstrate a link between perceptual polar angle asymmetries and cortical anatomy. Broadly, the results show a link between visual perception and the idiosyncratic cortical organization of V1 in neurotypical observers.SIGNIFICANCE STATEMENTContrast sensitivity is a fundamental property of the human visual system, which indexes the limits of what one can detect or discriminate – the window of visibility. Contrast sensitivity varies with stimulus location on the retina and across observers. These variations are not well understood. Using psychophysics and magnetic resonance imaging, we tested the hypothesis that contrast sensitivity depends on the amount of responsive tissue in primary visual cortex (V1). Individuals with greater contrast sensitivity had a larger V1. Further, within observers, variation in contrast sensitivity across polar angle locations matched the variation in V1 surface area representing those locations. These findings demonstrate a tight link between visual perception and cortical anatomy, both within and among people.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Jan C. Frankowski ◽  
Andrzej T. Foik ◽  
Alexa Tierno ◽  
Jiana R. Machhor ◽  
David C. Lyon ◽  
...  

AbstractPrimary sensory areas of the mammalian neocortex have a remarkable degree of plasticity, allowing neural circuits to adapt to dynamic environments. However, little is known about the effects of traumatic brain injury on visual circuit function. Here we used anatomy and in vivo electrophysiological recordings in adult mice to quantify neuron responses to visual stimuli two weeks and three months after mild controlled cortical impact injury to primary visual cortex (V1). We found that, although V1 remained largely intact in brain-injured mice, there was ~35% reduction in the number of neurons that affected inhibitory cells more broadly than excitatory neurons. V1 neurons showed dramatically reduced activity, impaired responses to visual stimuli and weaker size selectivity and orientation tuning in vivo. Our results show a single, mild contusion injury produces profound and long-lasting impairments in the way V1 neurons encode visual input. These findings provide initial insight into cortical circuit dysfunction following central visual system neurotrauma.


2021 ◽  
Author(s):  
Julien Corbo ◽  
John P McClure ◽  
Orhan Batuhan Erkat ◽  
Pierre-Olivier Polack

Learning is an essential cognitive mechanism that supports behavioral adaptation through neural processing adjustments. Learning was shown to modify sensory integration, yet the nature of those modifications and the computational advantages they confer remain unclear. By comparing the responses of primary visual cortex (V1) neurons evoked by oriented stimuli in naive mice and mice performing an orientation discrimination task, we found that the representations of rewarded and non-rewarded cues were sparser, more accurate and more stable in trained mice. This improved representation was associated with a distortion of the V1 orientation space such that stimuli close to the task cues were represented as the task stimuli themselves. This distortion was context-dependent, as it was absent in trained mice passively viewing the cues. Hence, visual processing in V1 was dynamically adapted to enhance the reliability of the representation of the learned cues and favor stimulus generalization in the task-relevant computational space.


2021 ◽  
Author(s):  
Dylan Barbera ◽  
Nicholas J. Priebe ◽  
Lindsey L. Glickfeld

AbstractSensory neurons not only encode stimuli that align with their receptive fields but are also modulated by context. For example, the responses of neurons in mouse primary visual cortex (V1) to gratings of their preferred orientation are modulated by the presence of superimposed orthogonal gratings (“plaids”). The effects of this modulation can be diverse: some neurons exhibit cross-orientation suppression while other neurons have larger responses to a plaid than its components. We investigated whether these diverse forms of masking could be explained by a unified circuit mechanism. We report that the suppression of cortical activity does not alter the effects of masking, ruling out cortical mechanisms. Instead, we demonstrate that the heterogeneity of plaid responses is explained by an interaction between stimulus geometry and orientation tuning. Highly selective neurons uniformly exhibit cross-orientation suppression, whereas in weakly-selective neurons masking depends on the spatial configuration of the stimulus, with effects transitioning systematically between suppression and facilitation. Thus, the diverse responses of mouse V1 neurons emerge as a consequence of the spatial structure of the afferent input to V1, with no need to invoke cortical interactions.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Brittany C. Clawson ◽  
Emily J. Pickup ◽  
Amy Ensing ◽  
Laura Geneseo ◽  
James Shaver ◽  
...  

AbstractLearning-activated engram neurons play a critical role in memory recall. An untested hypothesis is that these same neurons play an instructive role in offline memory consolidation. Here we show that a visually-cued fear memory is consolidated during post-conditioning sleep in mice. We then use TRAP (targeted recombination in active populations) to genetically label or optogenetically manipulate primary visual cortex (V1) neurons responsive to the visual cue. Following fear conditioning, mice respond to activation of this visual engram population in a manner similar to visual presentation of fear cues. Cue-responsive neurons are selectively reactivated in V1 during post-conditioning sleep. Mimicking visual engram reactivation optogenetically leads to increased representation of the visual cue in V1. Optogenetic inhibition of the engram population during post-conditioning sleep disrupts consolidation of fear memory. We conclude that selective sleep-associated reactivation of learning-activated sensory populations serves as a necessary instructive mechanism for memory consolidation.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Caitlin Siu ◽  
Justin Balsor ◽  
Sam Merlin ◽  
Frederick Federer ◽  
Alessandra Angelucci

AbstractThe mammalian sensory neocortex consists of hierarchically organized areas reciprocally connected via feedforward (FF) and feedback (FB) circuits. Several theories of hierarchical computation ascribe the bulk of the computational work of the cortex to looped FF-FB circuits between pairs of cortical areas. However, whether such corticocortical loops exist remains unclear. In higher mammals, individual FF-projection neurons send afferents almost exclusively to a single higher-level area. However, it is unclear whether FB-projection neurons show similar area-specificity, and whether they influence FF-projection neurons directly or indirectly. Using viral-mediated monosynaptic circuit tracing in macaque primary visual cortex (V1), we show that V1 neurons sending FF projections to area V2 receive monosynaptic FB inputs from V2, but not other V1-projecting areas. We also find monosynaptic FB-to-FB neuron contacts as a second motif of FB connectivity. Our results support the existence of FF-FB loops in primate cortex, and suggest that FB can rapidly and selectively influence the activity of incoming FF signals.


2000 ◽  
Vol 17 (1) ◽  
pp. 71-76 ◽  
Author(s):  
JOHN D. ALLISON ◽  
PETER MELZER ◽  
YUCHUAN DING ◽  
A.B. BONDS ◽  
VIVIEN A. CASAGRANDE

How neurons in the primary visual cortex (V1) of primates process parallel inputs from the magnocellular (M) and parvocellular (P) layers of the lateral geniculate nucleus (LGN) is not completely understood. To investigate whether signals from the two pathways are integrated in the cortex, we recorded contrast-response functions (CRFs) from 20 bush baby V1 neurons before, during, and after pharmacologically inactivating neural activity in either the contralateral LGN M or P layers. Inactivating the M layer reduced the responses of V1 neurons (n = 10) to all stimulus contrasts and significantly elevated (t = 8.15, P < 0.01) their average contrast threshold from 8.04 (± 4.1)% contrast to 22.46 (± 6.28)% contrast. M layer inactivation also significantly reduced (t = 4.06, P < 0.01) the average peak response amplitude. Inactivating the P layer did not elevate the average contrast threshold of V1 neurons (n = 10), but significantly reduced (t = 4.34, P < 0.01) their average peak response amplitude. These data demonstrate that input from the M pathway can account for the responses of V1 neurons to low stimulus contrasts and also contributes to responses to high stimulus contrasts. The P pathway appears to influence mainly the responses of V1 neurons to high stimulus contrasts. None of the cells in our sample, which included cells in all output layers of V1, appeared to receive input from only one pathway. These findings support the view that many V1 neurons integrate information about stimulus contrast carried by the LGN M and P pathways.


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