Evidence map›Paper›PMID 21808026›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Phasor approach to fluorescence lifetime microscopy distinguishes different metabolic states of germ cells in a live tissue.

Chiara Stringari, Amanda Cinquin, Olivier Cinquin, Michelle A Digman, Peter J Donovan, Enrico Gratton

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 239 papers.

0numbers the graph read from it
0cells of the map it votes in
239citing papers in PubMed
21.0field-weighted citation impact, top 1% 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

239 citing papers in PubMed, 433 citations in OpenAlex.

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  5. Metabolic trajectories in developing human neocortical neurons.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  11. Investigating Cellular Magnetic Bioeffects Using Two-Channel, Two-Photon Autofluorescence Lifetime Microscopy.IEEE transactions on molecular, biological, and multi-scale communications · 2026
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179 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Chiara StringariLaboratory of Fluorescence Dynamics, Biomedical Engineering Department, University of California, Irvine, CA 92697, USA.
Amanda Cinquin
Olivier Cinquin
Michelle A Digman
Peter J Donovan
Enrico Gratton
Fluorescence Innovations (United States) · USUniversity of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Uncover Strategies Used By Biological SystemsP50GM076516 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI NIE, QING · 2007 to 2016
$25.1M
PRIMATE RESOURCESP01HD047675 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SCHATTEN, GERALD · 2005 to 2010
$15.5M
Stem Cell Derivation from Germ CellsR01HD049488 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI DONOVAN, PETER JOHN · 2005 to 2009
$1.2M
NCI NIH HHS P30 CA062203NICHD NIH HHS P01 HD047675NICHD NIH HHS P01 HD47675NICHD NIH HHS R01 HD049488NICHD NIH HHS R01 HD49488NIGMS NIH HHS P50 GM076516NIGMS NIH HHS P50-GM076516PHS HHS P41-RRO3155
6 · The paper itself

Abstract

We describe a label-free imaging method to monitor stem-cell metabolism that discriminates different states of stem cells as they differentiate in living tissues. In this method we use intrinsic fluorescence biomarkers and the phasor approach to fluorescence lifetime imaging microscopy in conjunction with image segmentation, which we use to introduce the concept of the cell phasor. In live tissues we are able to identify intrinsic fluorophores, such as collagen, retinol, retinoic acid, porphyrin, flavins, and free and bound NADH. We have exploited the cell phasor approach to detect a trend in metabolite concentrations along the main axis of the Caenorhabditis elegans germ line. This trend is consistent with known changes in metabolic states during differentiation. The cell phasor approach to lifetime imaging provides a label-free, fit-free, and sensitive method to identify different metabolic states of cells during differentiation, to sense small changes in the redox state of cells, and may identify symmetric and asymmetric divisions and predict cell fate. Our method is a promising noninvasive optical tool for monitoring metabolic pathways during differentiation or disease progression, and for cell sorting in unlabeled tissues.

Indexed as

AnimalsBiomarkersCaenorhabditis elegansCell DifferentiationFluorescent DyesGerm CellsHalf-LifeMetabolismMetabolomicsMethodsMicroscopy, FluorescenceBiomarkersFluorescent Dyes

Identifiers

PMID21808026
PMCPMC3158156
OpenAlexW2047404221

What OpenQuestion holds

Textmetadata
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.