Evidence map›Paper›PMID 37751690›Full record

ArticleCell reports methods2023

Tailoring confocal microscopy for real-time analysis of photosynthesis at single-cell resolution.

Mattia Storti, Haythem Hsine, Clarisse Uwizeye, Olivier Bastien, Daniel P Yee, Fabien Chevalier, Johan Decelle, Cécile Giustini, Daniel Béal, Gilles Curien and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
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

12 authors at 2 institutions in 2 countries.

Mattia StortiGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Haythem HsineGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Clarisse UwizeyeGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Olivier BastienGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Daniel P YeeGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Fabien ChevalierGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Johan DecelleGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Cécile GiustiniGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Daniel BéalJBeamBio, 17000 La Rochelle, France.
Gilles CurienGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France.
Giovanni FinazziGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France. Electronic address: giovanni.finazzi@cea.fr.
Dimitri TolleterGrenoble Alpes University, CNRS, CEA, INRAE, IRIG-LPCV, 38000 Grenoble, France. Electronic address: dtolleter@gmail.com.
Centre National de la Recherche Scientifique · FRRoche (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photoautotrophs' environmental responses have been extensively studied at the organism and ecosystem level. However, less is known about their photosynthesis at the single-cell level. This information is needed to understand photosynthetic acclimation processes, as light changes as it penetrates cells, layers of cells, or organs. Furthermore, cells within the same tissue may behave differently, being at different developmental/physiological stages. Here, we describe an approach for single-cell and subcellular photophysiology based on the customization of confocal microscopy to assess chlorophyll fluorescence quenching by the saturation pulse method. We exploit this setup to (1) reassess the specialization of photosynthetic activities in developing tissues of non-vascular plants; (2) identify a specific subpopulation of phytoplankton cells in marine photosymbiosis, which consolidate energetic connections with their hosts; and (3) examine the link between light penetration and photoprotection responses inside the different tissues that constitute a plant leaf anatomy.

Indexed as

EcosystemPhotosynthesisAnimalsHeart RateMicroscopy, ConfocalPhytoplankton3D reconstructionconfocal microscopyCP: ImagingCP: Plantsfluorescence integrationlight penetrationnon-vascular and vascular plantsphotoprotectionphytoplankton

Identifiers

PMID37751690
PMCPMC10545909
OpenAlexW4386226532

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.