Acute requirement for the hippocampus in putatively conscious vision revealed by a mouse model of blindsight.
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- MiceVR for Michael Stryker, UCSF
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Overview
and 10 other authors
Vamsi Subraveti2, Narumi Mitchell2, Na Youn Jo2, Umais Khan5, Roger Anguera-Singla7, Zephyr Weinreich8, Hanna E. Willis9, Holly Bridge9, Michael P. Stryker5, Hillel Adesnik2,3- Institute for All Minds, Berkeley, CA 94704, USA
- Department of Molecular and Cellular Biology, University of California, Berkeley, Berkeley, CA 94720, USA
- Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720, USA
- Miller Institute for Basic Research, University of California, Berkeley, Berkeley, CA 94720, USA
- Department of Physiology, University of California, San Francisco, San Francisco, CA 94158, USA
- Lead contact
- Department of Neurology, Neuroscape and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA 94158, USA
- Swarthmore College, Swarthmore, PA 19081, USA
- Centre for Integrative Neuroimaging, Centre for Functional Magnetic Resonance Imaging of the Brain, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, UK
Abstract
The phenomenon of blindsight provides a unique opportunity to uncover brain areas important for conscious vision. Patients with blindsight lose the conscious experience of seeing while still being able to detect and locate visual stimuli. Blindsight occurs after damage to the primary visual cortex (V1). Rodents are likewise able to detect and locate visual stimuli after damage to V1, though whether they lose conscious vision as humans do is unclear. Here, we report the first mouse model of blindsight that provides evidence that removal of V1 causes mice to lose their putatively conscious vision. This loss occurs only if dLGN, a brain area in the thalamus that connects to V1, is damaged in addition to V1. We use this model to discover that suppressing the hippocampus acutely causes blindsight-like behavior. This suggests that the hippocampus functions in the intact brain to support conscious, but not unconscious, vision. Furthermore, while single, selective ablations of V1 or the hippocampus have only a minor effect on vision, simultaneous ablation causes blindsight-like behavior. These results suggest that V1 and the hippocampus can compensate for the permanent loss of the other for conscious vision, revealing a novel form of plasticity that supports conscious vision. Although never causally implicated in conscious visual perception, the hippocampus emerges as a candidate brain area critical for conscious experience. More broadly, this mouse model of blindsight will enable the interrogation and identification of the neural circuits that underlie conscious and unconscious vision.
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Recorded: type, language, journal, volume, issue, pages, dates, 30 authors, 10 keywords, 11 MeSH terms, 10 funders, 142 references, 5 RRIDs, 1 integrity notice.
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This paper
Bhatla, N., Cheong, K., Takahashi, S., Lay, C., Fiedeldey, M., Liang, K., Mao, M., Wu, Y.-F., Lu, S., Yun, K., Ganti, V., Tsao, R., Zhang, X., Mohamed, K. A., Chang, Y., Geng, Y., Dai, C., Liu, A. K., Lwin, Y. M., . . . Adesnik, H. (2026). Acute requirement for the hippocampus in putatively conscious vision revealed by a mouse model of blindsight. Current biology : CB, 36(8), 2043-2062.e7. https://
BibTeX
@article{bhatla2026acute
author = {Bhatla, Nikhil and Cheong, Kathryn and Takahashi, Sho and Lay, Corliss and Fiedeldey, Matthew and Liang, Kathleen and Mao, Mo and Wu, Yun-Fan and Lu, Sandy and Yun, Karis and Ganti, Viveca and Tsao, Raymond and Zhang, Xiaozhou and Mohamed, Kenzy A. and Chang, Yul and Geng, Yucong and Dai, Casey and Liu, Ashley K. and Lwin, Yee May and Kim, Heidi and Subraveti, Vamsi and Mitchell, Narumi and Jo, Na Youn and Khan, Umais and Anguera-Singla, Roger and Weinreich, Zephyr and Willis, Hanna E. and Bridge, Holly and Stryker, Michael P. and Adesnik, Hillel},
title = {{Acute requirement for the hippocampus in putatively conscious vision revealed by a mouse model of blindsight}},
journal = {Current biology : CB},
year = {2026},
month = apr,
volume = {36},
number = {8},
pages = {2043--2062.e7},
publisher = {Elsevier BV},
issn = {0960-9822},
doi = {10.1016/
url = {https://
pmid = {41962536},
pmcid = {PMC13393572}
}
RIS
TY - JOUR
AU - Bhatla, Nikhil
AU - Cheong, Kathryn
AU - Takahashi, Sho
AU - Lay, Corliss
AU - Fiedeldey, Matthew
AU - Liang, Kathleen
AU - Mao, Mo
AU - Wu, Yun-Fan
AU - Lu, Sandy
AU - Yun, Karis
AU - Ganti, Viveca
AU - Tsao, Raymond
AU - Zhang, Xiaozhou
AU - Mohamed, Kenzy A.
AU - Chang, Yul
AU - Geng, Yucong
AU - Dai, Casey
AU - Liu, Ashley K.
AU - Lwin, Yee May
AU - Kim, Heidi
AU - Subraveti, Vamsi
AU - Mitchell, Narumi
AU - Jo, Na Youn
AU - Khan, Umais
AU - Anguera-Singla, Roger
AU - Weinreich, Zephyr
AU - Willis, Hanna E.
AU - Bridge, Holly
AU - Stryker, Michael P.
AU - Adesnik, Hillel
TI - Acute requirement for the hippocampus in putatively conscious vision revealed by a mouse model of blindsight
T2 - Current biology : CB
J2 - Curr Biol
PY - 2026
DA - 2026/
VL - 36
IS - 8
SP - 2043
EP - 2062.e7
SN - 0960-9822
PB - Elsevier BV
DO - 10.1016/
UR - https://
LA - en
ER -
CSL-JSON
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