Evidence map›Paper›PMID 37214899›Full record

ArticlebioRxiv : the preprint server for biology2023

Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope.

Michael Hamersky, Khushi Tekale, L Matthew Winfree, Matthew Jm Rowan, Lindsey Seldin

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Michael HamerskyDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA, USA.
Khushi TekaleDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA, USA.
L Matthew WinfreeIndependent scholar, Snellville, GA.
Matthew Jm RowanDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA, USA.
Lindsey SeldinDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA, USA.
Emory University · US

Funding

Automated cell-type-specific electrophysiology for understanding circuit dysregulation in Alzheimer's DiseaseRF1AG079269 · NIA · EMORY UNIVERSITY · PI FOREST, CRAIG, ROWAN, MATTHEW J.M. · 2022 to 2024
$2.4M
Neuronal mechanisms of altered circuit excitability in early Alzheimer'sR56AG072473 · NIA · EMORY UNIVERSITY · PI ROWAN, MATTHEW J.M. · 2021 to 2021
$385k
The Role of Dermal Fibroblasts in Skin CancerIK2BX005370 · VA · VETERANS HEALTH ADMINISTRATION · PI SELDIN, LINDSEY NICOLE · 2022 to 2025
–
BLRD VA IK2 BX005370NIA NIH HHS R56 AG072473NIA NIH HHS RF1 AG079269
6 · The paper itself

Abstract

Understanding normal and aberrant in vivo cell behaviors is necessary to develop clinical interventions to thwart disease initiation and progression. It is therefore critical to optimize imaging approaches that facilitate the observation of cell dynamics in situ, where tissue structure and composition remain unperturbed. The epidermis is the body's outermost barrier as well as the source of the most prevalent human cancers, namely cutaneous skin carcinomas. The accessibility of skin tissue presents a unique opportunity to monitor epithelial and dermal cell behaviors in intact animals using noninvasive intravital microscopy. Nevertheless, this sophisticated imaging approach has primarily been achieved using upright multiphoton microscopes, which represents a significant barrier-for-entry for most investigators. In this study, we present a custom-designed 3D-printed microscope stage insert suitable for use with inverted confocal microscopes that streamlines long-term intravital imaging of ear skin in live transgenic mice. We believe this versatile invention, which may be customized to fit the inverted microscope brand and model of choice, as well as adapted to image additional organ systems, will prove invaluable to the greater scientific research community by significantly enhancing the accessibility of intravital microscopy. This technological advancement is critical to bolster our understanding of live cell dynamics in both normal and disease contexts. SUMMARY: A new tool to simplify intravital imaging using inverted confocal microscopy.

Identifiers

PMID37214899
PMCPMC10197696
OpenAlexW4376271180

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.