Evidence map›Paper›PMID 36463346›Full record

ArticleCommunications biology2022

Volumetric imaging of fast cellular dynamics with deep learning enhanced bioluminescence microscopy.

Luis Felipe Morales-Curiel, Adriana Carolina Gonzalez, Gustavo Castro-Olvera, Li-Chun Lynn Lin, Malak El-Quessny, Montserrat Porta-de-la-Riva, Jacqueline Severino, Laura Battle Morera, Valeria Venturini, Verena Ruprecht and 3 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 21 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

13 authors at 4 institutions in 1 country.

Luis Felipe Morales-CurielICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
Adriana Carolina Gonzalez *ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
Gustavo Castro-Olvera *ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
Li-Chun Lynn LinICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.ORCID 0000-0002-3025-6627
Malak El-QuessnyICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
Montserrat Porta-de-la-RivaICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
Jacqueline SeverinoCenter for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0001-6959-0342
Laura Battle MoreraCenter for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Valeria VenturiniCenter for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0003-2526-6473
Verena RuprechtCenter for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0003-4088-8633
Diego RamalloICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
Pablo Loza-AlvarezICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.ORCID 0000-0002-3129-1213
Michael KriegICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain. michael.krieg@icfo.eu.ORCID 0000-0003-0501-5036
Institute of Photonic Sciences · ESCentre for Genomic Regulation · ESInstitució Catalana de Recerca i Estudis Avançats · ESUniversitat Pompeu Fabra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bioluminescence microscopy is an appealing alternative to fluorescence microscopy, because it does not depend on external illumination, and consequently does neither produce spurious background autofluorescence, nor perturb intrinsically photosensitive processes in living cells and animals. The low photon emission of known luciferases, however, demands long exposure times that are prohibitive for imaging fast biological dynamics. To increase the versatility of bioluminescence microscopy, we present an improved low-light microscope in combination with deep learning methods to image extremely photon-starved samples enabling subsecond exposures for timelapse and volumetric imaging. We apply our method to image subcellular dynamics in mouse embryonic stem cells, epithelial morphology during zebrafish development, and DAF-16 FoxO transcription factor shuttling from the cytoplasm to the nucleus under external stress. Finally, we concatenate neural networks for denoising and light-field deconvolution to resolve intracellular calcium dynamics in three dimensions of freely moving Caenorhabditis elegans.

Indexed as

Deep LearningAnimalsCaenorhabditis elegansCell NucleusCytoplasmMiceMicroscopy, FluorescenceZebrafish

Identifiers

PMID36463346
PMCPMC9719505
OpenAlexW4310780840

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.