Success in many real-world tasks depends on our ability to dynamically track hidden states of the world. We hypothesized that neural populations estimate these states by processing sensory history through recurrent interactions which reflect the internal model of the world. To test this, we recorded brain activity in posterior parietal cortex (PPC) of monkeys navigating by optic flow to a hidden target location within a virtual environment, without explicit position cues. In addition to sequential neural dynamics and strong interneuronal interactions, we found that the hidden state - monkey's displacement from the goal - was encoded in single neurons, and could be dynamically decoded from population activity. The decoded estimates predicted navigation performance on individual trials. Task manipulations that perturbed the world model induced substantial changes in neural interactions, and modified the neural representation of the hidden state, while representations of sensory and motor variables remained stable. The findings were recapitulated by a task-optimized recurrent neural network model, suggesting that task demands shape the neural interactions in PPC, leading them to embody a world model that consolidates information and tracks task-relevant hidden states. Natural behaviors induce changes to hidden states of the world that may be vital to track. Here, in monkeys navigating virtually to hidden goals, the authors show that neural interactions in the posterior parietal cortex play a role in tracking displacement from an unobservable goal.
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Nihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Tokyo Metropolitan Inst Neurosci, Dept Syst Neurosci, Tokyo, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Sawada, Kaori
Miyachi, Shigehiro
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Kyoto Univ, Primate Res Inst, Sect Brain Sci, Kyoto 6068501, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Miyachi, Shigehiro
Yamashita, Akiko
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Nihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Yamashita, Akiko
Katsuyama, Narumi
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Nihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Katsuyama, Narumi
Imanishi, Michiko
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Tokyo Metropolitan Inst Neurosci, Dept Syst Neurosci, Tokyo, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Imanishi, Michiko
Kuroda, Teiko
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Tokyo Metropolitan Inst Neurosci, Dept Syst Neurosci, Tokyo, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Kuroda, Teiko
Taira, Masato
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Nihon Univ, Adv Res Inst Sci & Human, Tokyo 102, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan
Taira, Masato
Takada, Masahiko
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Tokyo Metropolitan Inst Neurosci, Dept Syst Neurosci, Tokyo, JapanNihon Univ, Sch Med Sci, Dept Appl Syst Neurosci, Tokyo 102, Japan