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Keypoint-based modeling reveals fine-grained body pose tuning in superior temporal sulcus neurons

Author

Listed:
  • Rajani Raman

    (KU Leuven
    KU Leuven)

  • Anna Bognár

    (KU Leuven
    KU Leuven)

  • Ghazaleh Ghamkhari Nejad

    (KU Leuven
    KU Leuven)

  • Albert Mukovskiy

    (University Clinic Tübingen)

  • Lucas Martini

    (University Clinic Tübingen)

  • Martin Giese

    (University Clinic Tübingen)

  • Rufin Vogels

    (KU Leuven
    KU Leuven)

Abstract

Body pose and orientation serve as vital visual signals in primate non-verbal social communication. Leveraging deep learning algorithms that extract body poses from videos of behaving monkeys, applied to a monkey avatar, we investigated neural tuning for pose and viewpoint, targeting fMRI-defined mid and anterior Superior Temporal Sulcus (STS) body patches. We modeled the pose and viewpoint selectivity of the units with keypoint-based principal component regression with cross-validation and applied model inversion as a key approach to identify effective body parts and views. Mid STS units were effectively modeled using view-dependent 2D keypoint representations, revealing that their responses were driven by specific body parts that differed among neurons. Some anterior STS units exhibited better predictive performances with a view-dependent 3D model. On average, anterior STS units were better fitted by a keypoint-based model incorporating mirror-symmetric viewpoint tuning than by view-dependent 2D and 3D keypoint models. However, in both regions, a view-independent keypoint model resulted in worse predictive performance. This keypoint-based approach provides insights into how the primate visual system encodes socially relevant body cues, deepening our understanding of body pose representation in the STS.

Suggested Citation

  • Rajani Raman & Anna Bognár & Ghazaleh Ghamkhari Nejad & Albert Mukovskiy & Lucas Martini & Martin Giese & Rufin Vogels, 2025. "Keypoint-based modeling reveals fine-grained body pose tuning in superior temporal sulcus neurons," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-60945-5
    DOI: 10.1038/s41467-025-60945-5
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    References listed on IDEAS

    as
    1. Pinglei Bao & Liang She & Mason McGill & Doris Y. Tsao, 2020. "A map of object space in primate inferotemporal cortex," Nature, Nature, vol. 583(7814), pages 103-108, July.
    2. Rishi Rajalingham & Kohitij Kar & Sachi Sanghavi & Stanislas Dehaene & James J. DiCarlo, 2020. "The inferior temporal cortex is a potential cortical precursor of orthographic processing in untrained monkeys," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
    3. Praneet C. Bala & Benjamin R. Eisenreich & Seng Bum Michael Yoo & Benjamin Y. Hayden & Hyun Soo Park & Jan Zimmermann, 2020. "Automated markerless pose estimation in freely moving macaques with OpenMonkeyStudio," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
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