98%
921
2 minutes
20
Spatiotemporal patterns of neural activity generate brain functions, such as perception, memory, and behavior. Four-dimensional (4-D: x, y, z, t) analyses of such neural activity will facilitate understanding of brain functions. However, conventional two-photon microscope systems observe single-plane brain tissue alone at a time with cellular resolution. It faces a trade-off between the spatial resolution in the x-, y-, and z-axes and the temporal resolution by a limited point-by-point scan speed. To overcome this trade-off in 4-D imaging, we developed a holographic two-photon microscope for dual-plane imaging. A spatial light modulator (SLM) provided an additional focal plane at a different depth. Temporal multiplexing of split lasers with an optical chopper allowed fast imaging of two different focal planes. We simultaneously recorded the activities of neurons on layers 2/3 and 5 of the cerebral cortex in awake mice in vivo. The present study demonstrated the proof-of-concept of dual-plane two-photon imaging of neural circuits by using the temporally multiplexed SLM-based microscope. The temporally multiplexed holographic microscope, combined with in vivo labeling with genetically encoded probes, enabled 4-D imaging and analysis of neural activities at cellular resolution and physiological timescales. Large-scale 4-D imaging and analysis will facilitate studies of not only the nervous system but also of various biological systems.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.neures.2021.02.001 | DOI Listing |
The spatial organization and dynamics of a genome are central to gene regulation. While a comprehensive understanding of chromatin organization in the human nucleus has been achieved using fixed-cell methods, measuring the dynamics of specific genomic regions over extended periods in individual living cells remains challenging. Here, we present a robust and fully genetically encoded system for fluorescent labeling and long-term tracking of any accessible non-repetitive genomic locus in live human cells using fluorogenic and replenishable nanobody array fusions of the dCas9, and compact polycistronic single guide (sg)RNAs.
View Article and Find Full Text PDFACS Sens
September 2025
Faculty of Biology, Lomonosov Moscow State University, Moscow, Russian Federation 119991.
Fluorogen-activating proteins are powerful molecular tools for microscopy, including functional imaging. These proteins serve as an alternative to GFP-like proteins, as they do not require oxygen for chromophore maturation. However, the restricted selectivity of proteins to chromophores, combined with the limited number of spectral channels of conventional fluorescent microscopes, hinders the development of multicolor synthetic dyes.
View Article and Find Full Text PDFDevelopment
September 2025
Regenerative Medicine Program, Ottawa Hospital Research Institute (OHRI), Ottawa, ON, K1H 8L6, Canada.
During development, neural progenitor cells modify their output over time to produce different types of neurons and glia in chronological sequences. Epigenetic processes have been shown to regulate neural progenitor potential, but the underlying mechanisms are not well understood. Here, we generated retina-specific conditional knockouts (cKOs) in the key nucleosome remodeller Chd4.
View Article and Find Full Text PDFActa Pharm Sin B
August 2025
School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
The precise and rapid monitoring of multiple organ dysfunction is crucial in drug discovery. Traditional methods, such as pathological analysis, are often time-consuming and inefficient. Here, we developed a multiplexed near-infrared window two (NIR-II) fluorescent bioimaging method that allows for real-time, rapid, and quantitative assessment of multiple organ dysfunctions.
View Article and Find Full Text PDFCompact, scalable, and multiplexed fluorescence lifetime sensors are of great interest for point-of-care diagnostics. However, current solutions either lack broad-range wavelength-tuning capabilities or involve complex optical setups that hinder miniaturization. On-chip entangled photon sources offer a promising alternative for time-resolved spectroscopy with their strong temporal correlations, tunable spectral characteristics, and small footprints.
View Article and Find Full Text PDF