Evidence map›Paper›PMID 35773755›Full record

ArticleJournal of biomedical optics2022

Functional imaging with dynamic quantitative oblique back-illumination microscopy.

Paloma Casteleiro Costa, Bryan Wang, Caroline Filan, Annie Bowles-Welch, Carolyn Yeago, Krishnendu Roy, Francisco E Robles

Open access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

15 citing papers in PubMed, 27 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Paloma Casteleiro CostaGeorgia Institute of Technology, School of Electrical and Computer Engineering, Atlanta, Georgia, United States.
Bryan WangGeorgia Institute of Technology and Emory University, Wallace H. Coulter Department of Biomedical En, United States.
Caroline FilanGeorgia Institute of Technology, Nuclear & Radiological Engineering and Medical Physics Program, Atl, United States.
Annie Bowles-WelchGeorgia Institute of Technology and Emory University, Wallace H. Coulter Department of Biomedical En, United States.
Carolyn YeagoGeorgia Institute of Technology, Marcus Center for Therapeutic Cell Characterization and Manufacturi, United States.
Krishnendu RoyGeorgia Institute of Technology and Emory University, Wallace H. Coulter Department of Biomedical En, United States.
Francisco E RoblesGeorgia Institute of Technology, School of Electrical and Computer Engineering, Atlanta, Georgia, United States.
Georgia Institute of Technology · USThe Wallace H. Coulter Department of Biomedical Engineering · US

Funding

Stimulated Raman scattering spectroscopic optical coherence tomography (SRS-SOCT) for label-free molecular imaging of brain tumor pathologyR21CA223853 · NCI · GEORGIA INSTITUTE OF TECHNOLOGY · PI ROBLES, FRANCISCO E · 2018 to 2020
$606k
In-line, Non-invasive, Real-time 3D Quantitative Phase Microscopy for OrganoidsR21NS117067 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG, ROBLES, FRANCISCO E · 2020 to 2020
$426k
NCI NIH HHS R21 CA223853NINDS NIH HHS R21 NS117067
6 · The paper itself

Abstract

significanceQuantitative oblique back-illumination microscopy (qOBM) is a recently developed label-free imaging technique that enables 3D quantitative phase imaging of thick scattering samples with epi-illumination. Here, we propose dynamic qOBM to achieve functional imaging based on subcellular dynamics, potentially indicative of metabolic activity. We show the potential utility of this novel technique by imaging adherent mesenchymal stromal cells (MSCs) grown in bioreactors, which can help address important unmet needs in cell manufacturing for therapeutics.

aimWe aim to develop dynamic qOBM and demonstrate its potential for functional imaging based on cellular and subcellular dynamics. APPROACH: To obtain functional images with dynamic qOBM, a sample is imaged over a period of time and its temporal signals are analyzed. The dynamic signals display an exponential frequency response that can be analyzed with phasor analysis. Functional images of the dynamic signatures are obtained by mapping the frequency dynamic response to phasor space and color-coding clustered signals.

resultsFunctional imaging with dynamic qOBM provides unique information related to subcellular activity. The functional qOBM images of MSCs not only improve conspicuity of cells in complex environments (e.g., porous micro-carriers) but also reveal two distinct cell populations with different dynamic behavior.

conclusionsIn this work we present a label-free, fast, and scalable functional imaging approach to study and intuitively display cellular and subcellular dynamics. We further show the potential utility of this novel technique to help monitor adherent MSCs grown in bioreactors, which can help achieve quality-by-design of cell products, a significant unmet need in the field of cell therapeutics. This approach also has great potential for dynamic studies of other thick samples, such as organoids.

Indexed as

Mesenchymal Stem CellsMicroscopyImaging, Three-DimensionalLightingdynamicfunctional imaginglabel-freemicroscopyquantitative phase imagingstem cells

Identifiers

PMID35773755
PMCPMC9243522
OpenAlexW4283752816

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.