Evidence map›Paper›PMID 40011620›Full record

ArticleCommunications biology2025

DeepCristae, a CNN for the restoration of mitochondria cristae in live microscopy images.

Salomé Papereux, Ludovic Leconte, Cesar Augusto Valades-Cruz, Tianyan Liu, Julien Dumont, Zhixing Chen, Jean Salamero, Charles Kervrann, Anaïs Badoual

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Salomé Papereux *SERPICO Project Team, Centre Inria de l'Université de Rennes, Rennes, France.ORCID http://orcid.org/0009-0000-0612-7780
Ludovic Leconte *SERPICO Project Team, Centre Inria de l'Université de Rennes, Rennes, France.
Cesar Augusto Valades-Cruz *SERPICO Project Team, Centre Inria de l'Université de Rennes, Rennes, France.ORCID http://orcid.org/0000-0002-1786-8207
Tianyan LiuCollege of Future Technology, Institute of Molecular Medicine, National Biomedical Imaging Center, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking-Tsinghua Center for Life Science, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Julien DumontCIRB Microscopy Facility, Collège de France, UMR 7241 CNRS, Inserm U1050, Paris, France.
Zhixing ChenCollege of Future Technology, Institute of Molecular Medicine, National Biomedical Imaging Center, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking-Tsinghua Center for Life Science, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.ORCID http://orcid.org/0000-0001-5962-7359
Jean SalameroSERPICO Project Team, Centre Inria de l'Université de Rennes, Rennes, France.ORCID http://orcid.org/0000-0002-2610-5826
Charles KervrannSERPICO Project Team, Centre Inria de l'Université de Rennes, Rennes, France.ORCID http://orcid.org/0000-0001-6263-0452
Anaïs BadoualSERPICO Project Team, Centre Inria de l'Université de Rennes, Rennes, France. anais.badoual@inria.fr.ORCID http://orcid.org/0000-0001-7303-6344

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-INBS-04-07Agence Nationale de la Recherche (French National Research Agency) ANR- 11-LABX-0038
6 · The paper itself

Abstract

Mitochondria play an essential role in the life cycle of eukaryotic cells. However, we still don't know how their ultrastructure, like the cristae of the inner membrane, dynamically evolves to regulate these fundamental functions, in response to external conditions or during interaction with other cell components. Although high-resolution fluorescent microscopy coupled with recently developed innovative probes can reveal this structural organization, their long-term, fast and live 3D imaging remains challenging. To address this problem, we have developed a CNN, called DeepCristae, to restore mitochondria cristae in low spatial resolution microscopy images. Our network is trained from 2D STED images using a novel loss specifically designed for cristae restoration. To efficiently increase the size of the training set, we also developed a random image patch sampling centered on mitochondrial areas. To evaluate DeepCristae, quantitative assessments are carried out using metrics we derived by focusing on the mitochondria and cristae pixels rather than on the whole image as usual. Depending on the conditions of use indicated, DeepCristae works well on broad microscopy modalities (Stimulated Emission Depletion (STED), Live-SR, AiryScan and LLSM). It is ultimately applied in the context of mitochondrial network dynamics during interaction with endo/lysosome membranes.

Indexed as

MitochondriaMitochondrial MembranesAnimalsHumansImaging, Three-DimensionalMicroscopy, Fluorescence

Identifiers

PMID40011620
PMCPMC11865493

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Registered trials

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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.