Synaptic wiring motifs in posterior parietal cortex support decision-making
Aaron T. Kuan,
Giulio Bondanelli,
Laura N. Driscoll,
Julie Han,
Minsu Kim,
David G. C. Hildebrand,
Brett J. Graham,
Daniel E. Wilson,
Logan A. Thomas,
Stefano Panzeri (),
Christopher D. Harvey () and
Wei-Chung Allen Lee ()
Additional contact information
Aaron T. Kuan: Harvard Medical School
Giulio Bondanelli: Istituto Italiano di Tecnologia
Laura N. Driscoll: Harvard Medical School
Julie Han: Harvard Medical School
Minsu Kim: Harvard Medical School
David G. C. Hildebrand: Harvard Medical School
Brett J. Graham: Harvard Medical School
Daniel E. Wilson: Harvard Medical School
Logan A. Thomas: Harvard Medical School
Stefano Panzeri: Istituto Italiano di Tecnologia
Christopher D. Harvey: Harvard Medical School
Wei-Chung Allen Lee: Harvard Medical School
Nature, 2024, vol. 627, issue 8003, 367-373
Abstract:
Abstract The posterior parietal cortex exhibits choice-selective activity during perceptual decision-making tasks1–10. However, it is not known how this selective activity arises from the underlying synaptic connectivity. Here we combined virtual-reality behaviour, two-photon calcium imaging, high-throughput electron microscopy and circuit modelling to analyse how synaptic connectivity between neurons in the posterior parietal cortex relates to their selective activity. We found that excitatory pyramidal neurons preferentially target inhibitory interneurons with the same selectivity. In turn, inhibitory interneurons preferentially target pyramidal neurons with opposite selectivity, forming an opponent inhibition motif. This motif was present even between neurons with activity peaks in different task epochs. We developed neural-circuit models of the computations performed by these motifs, and found that opponent inhibition between neural populations with opposite selectivity amplifies selective inputs, thereby improving the encoding of trial-type information. The models also predict that opponent inhibition between neurons with activity peaks in different task epochs contributes to creating choice-specific sequential activity. These results provide evidence for how synaptic connectivity in cortical circuits supports a learned decision-making task.
Date: 2024
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DOI: 10.1038/s41586-024-07088-7
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