Detail of Fig3B_2PE


Project
SSBD:Repository
Title
2PE image of the neuronal dendrites in 4 micrometer depth of fixed Thy1-YFP-H mouse brain
Description
2PE (Two-photon excitation microscopy) image of the neuronal dendrites in 4 micrometer depth of fixed Thy1-YFP-H mouse brain slice.
Release, Updated
2026-07-08
License
CC BY 4.0
Kind
Image data
File Formats
.tif
Data size
256.5 KB

Organism
Mus musculus ( NCBI:txid10090 )
Strain(s)
B6.Cg-Tg(Thy1-YFP)HJrs/J
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
Cellular Component (CC)
dendritic spine
Biological Imaging Method
two-photon laser scanning microscopy ( Fbbi:00000254 )
X scale
0.04 micrometer
Y scale
0.04 micrometer
Z scale
-
T scale
-

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
Ishii H, Otomo K, Chang CP, Yamasaki M, Watanabe M, Yokoyama H, Nemoto T. All-synchronized picosecond pulses and time-gated detection improve the spatial resolution of two-photon STED microscopy in brain tissue imaging. PLoS One. 2023 Aug 24;18(8):e0290550.
Related paper(s)

Hirokazu Ishii, Kohei Otomo, Ching-Pu Chang, Miwako Yamasaki, Masahiko Watanabe, Hiroyuki Yokoyama, Tomomi Nemoto (2023) All-synchronized picosecond pulses and time-gated detection improve the spatial resolution of two-photon STED microscopy in brain tissue imaging., PLOS ONE, Volume 18, Number 8

Published in 2023 (Electronic publication in Aug. 24, 2023, midnight )

(Abstract) Super-resolution in two-photon excitation (2PE) microscopy offers new approaches for visualizing the deep inside the brain functions at the nanoscale. In this study, we developed a novel 2PE stimulated-emission-depletion (STED) microscope with all-synchronized picosecond pulse light sources and time-gated fluorescence detection, namely, all-pulsed 2PE-gSTED microscopy. The implementation of time-gating is critical to excluding undesirable signals derived from brain tissues. Even in a case using subnanosecond pulses for STED, the impact of time-gating was not negligible; the spatial resolution in the image of the brain tissue was improved by approximately 1.4 times compared with non time-gated image. This finding demonstrates that time-gating is more useful than previously thought for improving spatial resolution in brain tissue imaging. This microscopy will facilitate deeper super-resolution observation of the fine structure of neuronal dendritic spines and the intracellular dynamics in brain tissue.

Contact
Tomomi Nemoto , National Institutes of Natural Sciences , Exploratory Research Center on Life and Living Systems , Exploratory Research Center on Life and Living Systems
Contributors

OMERO Dataset
OMERO Project
Source