Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Safety considerations of gene-based therapies for Alzheimer's disease.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same author

STIMscope: centimeter-scale all-optical imaging and patterned optogenetic manipulation at single-cell resolution.

bioRxiv : the preprint server for biology·2026
Same author

The prefrontal cortex controls memory organization in the hippocampus.

Nature neuroscience·2026
Same author

Rapid formation of non-spatial hippocampal representations consistent with behavioral timescale synaptic plasticity is modulated by entorhinal input.

Nature communications·2026
Same author

Single-Nucleus Transcriptomics Reveals Cell Type-Specific Remodeling and Epilepsy-Associated Microglia.

bioRxiv : the preprint server for biology·2026
Same author

MiniFAST: a sensitive and fast miniaturized microscope for <i>in vivo</i> neural recording.

Neurophotonics·2026

Related Experiment Video

Updated: Sep 13, 2025

Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States
06:25

Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States

Published on: January 19, 2024

1.1K

Open-source, high performance miniature 2-photon microscopy systems for freely behaving animals.

Blake A Madruga1,2,3, Conor C Dorian1,2, Long Yang1

  • 1Department of Neurology, UCLA School of Medicine, Los Angeles, CA, USA.

Nature Communications
|August 2, 2025
PubMed
Summary

Researchers developed an open-source miniature 2-photon (2P) microscope for deep brain calcium imaging. This UCLA 2P Miniscope enables high-resolution neural activity recording in deep brain structures and dendrites.

More Related Videos

Transpupillary Two-Photon In Vivo Imaging of the Mouse Retina
09:03

Transpupillary Two-Photon In Vivo Imaging of the Mouse Retina

Published on: February 13, 2021

4.5K
Longitudinal Two-Photon Imaging of Dorsal Hippocampal CA1 in Live Mice
09:34

Longitudinal Two-Photon Imaging of Dorsal Hippocampal CA1 in Live Mice

Published on: June 19, 2019

16.3K

Related Experiment Videos

Last Updated: Sep 13, 2025

Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States
06:25

Author Spotlight: Comparative Imaging of Neural Activity in Awake and Freely Moving States

Published on: January 19, 2024

1.1K
Transpupillary Two-Photon In Vivo Imaging of the Mouse Retina
09:03

Transpupillary Two-Photon In Vivo Imaging of the Mouse Retina

Published on: February 13, 2021

4.5K
Longitudinal Two-Photon Imaging of Dorsal Hippocampal CA1 in Live Mice
09:34

Longitudinal Two-Photon Imaging of Dorsal Hippocampal CA1 in Live Mice

Published on: June 19, 2019

16.3K

Area of Science:

  • Neuroscience
  • Biomedical Engineering
  • Optical Imaging

Background:

  • Calcium imaging is crucial for understanding neural circuit dynamics.
  • Miniaturized microscopes are needed for in vivo recordings in deep brain structures.
  • Existing technologies face limitations in light collection efficiency and field of view.

Purpose of the Study:

  • To introduce the UCLA 2P Miniscope, an open-source miniature 2-photon microscope.
  • To demonstrate its capability for recording calcium dynamics in deep neural structures and dendrites.
  • To provide open access to the design and building instructions.

Main Methods:

  • Developed a miniature 2-photon microscope utilizing two on-board silicon-based photon detectors.
  • Achieved a 445µm × 380µm field of view with electronic focusing over a 150µm range.
  • Tested the system by recording calcium dynamics in hippocampus place cells, retrosplenial cortex dendrites, and deep dentate granule cells.

Main Results:

  • The UCLA 2P Miniscope demonstrated effective calcium imaging in deep brain regions.
  • Achieved approximately 4-fold greater light collection compared to fiber bundle approaches.
  • Successfully recorded neural activity from neurons over 620µm deep during open field behavior.

Conclusions:

  • The UCLA 2P Miniscope is a powerful, open-source tool for advanced in vivo calcium imaging.
  • Its design facilitates recordings from deep neural structures and dendrites with high resolution.
  • Open-source availability promotes wider adoption and further development in neuroscience research.