ArticleBiomedical optics express2015
In vivo two-photon imaging of mouse hippocampal neurons in dentate gyrus using a light source based on a high-peak power gain-switched laser diode.
Article in Biomedical optics express, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.
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Who cites it
28 citing papers in PubMed, 91 citations in OpenAlex.
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- 110 μm thin endo-microscope for deep-brain in vivo observations of neuronal connectivity, activity and blood flow dynamics.Nature communications · 2023Article
- Fluorescence radial fluctuation enables two-photon super-resolution microscopy.Frontiers in cellular neuroscience · 2023Article
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- Optical clearing of living brains with MAGICAL to extendiScience · 2021Article
- Adaptive Optical Two-Photon Microscopy for Surface-Profiled Living Biological Specimens.ACS omega · 2021Article
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- Excitation and emission dual-wavelength confocal metalens designed directly in the biological tissue environment for two-photon micro-endoscopy.Biomedical optics express · 2020Article
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- Light needle microscopy with spatially transposed detection for axially resolved volumetric imaging.Scientific reports · 2019Article
- Two-photon STED nanoscopy realizing 100-nm spatial resolution utilizing high-peak-power sub-nanosecond 655-nm pulses.Biomedical optics express · 2019Article
- Light-sheet microscopy in the near-infrared II window.Nature methods · 2019Article
- Peeking into the sleeping brain: Using in vivo imaging in rodents to understand the relationship between sleep and cognition.Journal of neuroscience methods · 2019Review
- Wavelength agile multi-photon microscopy with a fiber amplified diode laser.Biomedical optics express · 2018Article
- Optical alignment device for two-photon microscopy.Biomedical optics express · 2018Article
- Advanced easySTED microscopy based on two-photon excitation by electrical modulations of light pulse wavefronts.Biomedical optics express · 2018Article
- Interferometric temporal focusing microscopy using three-photon excitation fluorescence.Biomedical optics express · 2018Article
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Authors and funding
9 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In vivo two-photon microscopy is an advantageous technique for observing the mouse brain at high resolution. In this study, we developed a two-photon microscopy method that uses a 1064-nm gain-switched laser diode-based light source with average power above 4 W, pulse width of 7.5-picosecond, repetition rate of 10-MHz, and a high-sensitivity photomultiplier tube. Using this newly developed two-photon microscope for in vivo imaging, we were able to successfully image hippocampal neurons in the dentate gyrus and obtain panoramic views of CA1 pyramidal neurons and cerebral cortex, regardless of age of the mouse. Fine dendrites in hippocampal CA1 could be imaged with a high peak-signal-to-background ratio that could not be achieved by titanium sapphire laser excitation. Finally, our system achieved multicolor imaging with neurons and blood vessels in the hippocampal region in vivo. These results indicate that our two-photon microscopy system is suitable for investigations of various neural functions, including the morphological changes undergone by neurons during physiological phenomena.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.