2P-FENDO-II: A fiber bundle microscope for all-optical, large field-of-view brain studies in freely moving mice

All-optical strategies enable identification of functional neuronal ensembles with calcium imaging and replay/alter their spatiotemporal activity with optogenetics to decipher their behavioral implications. We previously developed a fiber-coupled microscope enabling two-photon (2P) functional imaging and 2P holographic photostimulation with near-single-cell resolution in freely moving mice: 2P-FENDO. Here, we present a significantly optimized 2P-FENDO-II system that achieves a four-times-larger field of view and a more homogeneous light distribution across the field of view, both for imaging and photostimulation, while achieving better flexibility and thus optimal adaptation to the study of freely moving mice. We demonstrate the performance and versatility of 2P-FENDO-II in experiments targeting the somatosensory cortex, the visual cortex, or the cerebellar cortex, in which we show concomitant calcium imaging with jGCaMP7s and optogenetic control with ChRmine. These enhancements establish 2P-FENDO-II as a groundbreaking tool for all-optical interrogation of neuronal circuits on large volume in naturalistic situations.

Authors

Institutions

Publication Details

Journal
Cell Reports Methods
Published
2026-02-01
DOI
https://doi.org/10.1016/j.crmeth.2026.101305
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

2P-FENDO-II: A fiber bundle microscope for all-optical, large field-of-view brain studies in freely moving mice

Christophe Tourain, Antonio Lorca-Cámara, François G. C. Blot, Nicolò Accanto et al.
Cell Reports Methods
Advanced Fluorescence Microscopy Techniques
article

2P-FENDO-II: A fiber bundle microscope for all-optical, large field-of-view brain studies in freely moving mice

Christophe Tourain, Antonio Lorca-Cámara, François G. C. Blot, Nicolò Accanto, Dimitri Decombe, Maya Anquetil, Benoît C. Forget, Valentina Emiliani, Vincent de Sars
article en

Abstract

All-optical strategies enable identification of functional neuronal ensembles with calcium imaging and replay/alter their spatiotemporal activity with optogenetics to decipher their behavioral implications. We previously developed a fiber-coupled microscope enabling two-photon (2P) functional imaging and 2P holographic photostimulation with near-single-cell resolution in freely moving mice: 2P-FENDO. Here, we present a significantly optimized 2P-FENDO-II system that achieves a four-times-larger field of view and a more homogeneous light distribution across the field of view, both for imaging and photostimulation, while achieving better flexibility and thus optimal adaptation to the study of freely moving mice. We demonstrate the performance and versatility of 2P-FENDO-II in experiments targeting the somatosensory cortex, the visual cortex, or the cerebellar cortex, in which we show concomitant calcium imaging with jGCaMP7s and optogenetic control with ChRmine. These enhancements establish 2P-FENDO-II as a groundbreaking tool for all-optical interrogation of neuronal circuits on large volume in naturalistic situations.

Cell Reports MethodsVol. 6(2)
Centre National de la Recherche Scientifique (FR), Institut de la Vision (FR), Inserm (FR), Sorbonne Université (FR)
Openalex Percentile: Top 61%
Advanced Fluorescence Microscopy Techniques
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

2P-FENDO-II: A fiber bundle microscope for all-optical, large field-of-view brain studies in freely moving mice — Christophe Tourain, Antonio Lorca-Cámara, et al. · Cell Reports Methods (2026) | TGRS Research Map | TGRS