Evidence map›Paper›PMID 39911733›Full record

ArticleFrontiers in photonics2023

Incoherent color holography lattice light-sheet for subcellular imaging of dynamic structures.

Simon Alford, Christopher Mann, Jonathan Art, Mariana Potcoava

Abstract read
In one paragraph

Article in Frontiers in photonics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Simon AlfordDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, United States.
Christopher MannDepartment of Applied Physics and Materials Science, Northern Arizona University, Flagstaff, AZ, United States.
Jonathan ArtDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, United States.
Mariana PotcoavaDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, United States.

Funding

Regulation of exocytosis by direct Gbg blockade of fusionR01NS111749 · NINDS · VANDERBILT UNIVERSITY · PI ALFORD, SIMON T, HAMM, HEIDI E · 2019 to 2023
$2.0M
Optical and biophysical characterization of the vestibular peripheryR21DC017292 · NIDCD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ART, JONATHAN JAMES · 2019 to 2020
$440k
NIDCD NIH HHS R21 DC017292NINDS NIH HHS R01 NS111749
6 · The paper itself

Abstract

The purpose of the article is to explore the need and advantages of using the incoherent color holography lattice light-sheet (ICHLLS) to provide multiwavelength quantitative monitoring of 3D cellular dynamics in live tissue to further understand complex functions of cells and cellular compartments. We have explored the use of incoherent color holography lattice light-sheet to investigate colocalization of fluorescent markers in live cells in intact tissue. Neuronal structures provide an attractive target for incoherent color holography lattice light-sheet. The cells show a complex architecture in 3D space in which signaling both between cells and within subcellular structures requires colocalization of proteins and lipids to function. During activity and over long periods it is important in understanding these signaling functions in Parkinson's, Alzheimer's and motoneuron diseases within live cells in intact tissue. As a proof of concept this article recalls the key aspects in lattice light-sheet imaging and provides a description of the incoherent detection system configuration to actively control dual diffractive lenses phase-shifting at multiple excitation wavelengths sequentially, and per each z-galvo scanning level, with extended field-of-view. The incoherent color holography lattice light-sheet system will allow simultaneous recording of multidimensional object waves that contain intensity in 3D space, phase, and wavelength information. We measure colocalization of fluorescence indicators introduced into live cells in intact neural tissue.

Indexed as

colocalizationdigital holographic microscopyfluorescence microscopyIncoherent Color Holography Lattice Light-Sheetphase-shifting interferometry

Identifiers

PMID39911733
PMCPMC11798417

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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.