This work addresses a question of fundamental significance: how does sensory reafference help maintain perceptual stability during eye and head movements? For example, a rightward eye movement adds leftward motion to the retinal image. This self-produced retinal motion - reafference - must be discounted to compute real-world (e.g., object) motion. Whenever this operation fails, a stationary background seems moving, a phenomenon known as the Filehne illusion. A similar compensation for reafference is necessary when optic flow is used to estimate the direction of self-motion (i.e., heading). Indeed, when tested in the laboratory, subjects are remarkably good at compensating for smooth pursuit eye movements and accuracy is little affected. But where in the brain does this reafference compensation for pursuit take place? Here we propose a 2-pronged approach, where (i) we record simultaneously from the dorsal medial superior temporal area (MSTd), the ventral intraparietal area (VIP), the visual posterior sylvian (VPS) and parieto-occipital area V6 and characterize how visual motion and/or heading tuning changes during pursuit eye and head movements (aim 1), as well as the reference frames in which visual and vestibular heading signals are represented (aim 2);and (ii) we use reversible chemical inactivation to silence neural activity in these areas while monitoring the animals'ability to perform a heading direction discrimination task in the presence of pursuit eye and head movements, as well as the magnitude and direction of the Filehne illusion. Importantly, our experimental design circumvents many technical and interpretational problems in previous studies, whereas optimal decoding analysis will address, not only single neuron, but also population responses. The general principles that we uncover should have wide application to problems in systems neuroscience, ranging from the electric fish to human cognition. In terms of health-related significance, although uncommon, loss of perceptual compensation for reafference has disabling consequences. Recent studies have shown that misattributions of agency in schizophrenia are based on imprecise predictions about the sensory consequences of one's actions;thus, understanding the neural basis of reafference will be important for further investigating this complex cognitive disorder. In addition, this work also addresses the neural basis of self-motion perception and navigation, which is relevant to spatial disorientation deficits in Alzheimer's disease.

Public Health Relevance

The general principles that we uncover should have wide application to problems in systems neuroscience, ranging from the electric fish to human cognition. In terms of health-related significance, although uncommon, loss of perceptual compensation for reafference has disabling consequences. Recent studies have shown that misattributions of agency in schizophrenia are based on imprecise predictions about the sensory consequences of one's actions;thus, understanding the neural basis of reafference will be important for further investigating this complex cognitive disorder. In addition, this work also addresses the neural basis of self-motion perception and navigation, which is relevant to spatial disorientation deficits in Alzheimer's disease.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY017866-06
Application #
8257476
Study Section
Special Emphasis Panel (ZRG1-IFCN-N (02))
Program Officer
Steinmetz, Michael A
Project Start
2007-02-01
Project End
2012-03-31
Budget Start
2012-02-01
Budget End
2012-03-31
Support Year
6
Fiscal Year
2012
Total Cost
$63,334
Indirect Cost
$21,667
Name
Washington University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Yau, Jeffrey M; DeAngelis, Gregory C; Angelaki, Dora E (2015) Dissecting neural circuits for multisensory integration and crossmodal processing. Philos Trans R Soc Lond B Biol Sci 370:20140203
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Sunkara, Adhira; DeAngelis, Gregory C; Angelaki, Dora E (2015) Role of visual and non-visual cues in constructing a rotation-invariant representation of heading in parietal cortex. Elife 4:
Angelaki, Dora E (2014) How Optic Flow and Inertial Cues Improve Motion Perception. Cold Spring Harb Symp Quant Biol 79:141-8
Gu, Yong; Angelaki, Dora E; DeAngelis, Gregory C (2014) Contribution of correlated noise and selective decoding to choice probability measurements in extrastriate visual cortex. Elife 3:
Chen, Xiaodong; DeAngelis, Gregory C; Angelaki, Dora E (2014) Eye-centered visual receptive fields in the ventral intraparietal area. J Neurophysiol 112:353-61
Chen, Aihua; Deangelis, Gregory C; Angelaki, Dora E (2013) Functional specializations of the ventral intraparietal area for multisensory heading discrimination. J Neurosci 33:3567-81
Chen, Xiaodong; Deangelis, Gregory C; Angelaki, Dora E (2013) Diverse spatial reference frames of vestibular signals in parietal cortex. Neuron 80:1310-21
Chen, Xiaodong; DeAngelis, Gregory C; Angelaki, Dora E (2013) Eye-centered representation of optic flow tuning in the ventral intraparietal area. J Neurosci 33:18574-82

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