Functional bipartite invariance in mouse primary visual cortex receptive fields

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Zhiwei Ding, Dat Tran, Kayla Ponder, Zhuokun Ding, Rachel Froebe, Lydia Ntanavara, Paul G Fahey, Erick Cobos, Luca Baroni, Maria Diamantaki, Eric Y Wang, Andersen Chang, Stelios Papadopoulos, Jiakun Fu, Taliah Muhammad, Christos Papadopoulos, Santiago A Cadena, Alexandros Evangelou, Konstantin Willeke, Fabio Anselmi, Sophia Sanborn, Jan Antolik, Emmanouil Froudarakis, Saumil Patel, Edgar Y Walker, Jacob Reimer, Fabian H Sinz, Alexander S Ecker, Katrin Franke, Xaq Pitkow, Andreas S Tolias

Nat Neurosci. 2026 Feb 25. doi: 10.1038/s41593-026-02213-3. Online ahead of print.

ABSTRACT

Sensory systems support generalization by representing features that persist under input variation; however, identifying the neuronal basis of these invariances remains difficult due to high-dimensional and nonlinear neural computations. Here we leverage the inception loop paradigm, iterating between large-scale recordings, predictive models and in silico experiments with in vivo verification, to characterize neuronal invariances in mouse primary visual cortex (V1). We synthesize varied exciting inputs (VEIs), dissimilar images that drive target neurons. These VEIs revealed a new bipartite invariance: one subfield encodes a shift-tolerant high-frequency texture and the other encodes a fixed low-frequency pattern. This division aligns with object boundaries defined by spatial frequency differences in highly activating images, suggesting a contribution to segmentation. Analysis of the MICrONS dataset revealed a hierarchy of excitatory neurons in mouse V1 layers 2/3: postsynaptic neurons exhibited greater invariance than their presynaptic inputs, while neurons with lower invariance formed more connections. Together, these results provide insights and scalable methodology for mapping neuronal invariances.

PMID:41741659 | DOI:10.1038/s41593-026-02213-3