Evidence map›Paper›PMID 41184551›Full record

ArticleNature methods2025

ESPRESSO: spatiotemporal omics based on organelle phenotyping.

Lorenzo Scipioni, Giulia Tedeschi, Mariana X Navarro, Yunlong Y Jia, Songning Zhu, Lila P Halbers, Melody Di Bona, Scott X Atwood, Jennifer A Prescher, Enrico Gratton and 1 more

Abstract read
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In one paragraph

Article in Nature methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Algebraic Representation of Mitochondrial Dynamics.Bulletin of mathematical biology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. 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

11 authors.

Lorenzo Scipioni *Centre de Recherche en Cancérologie de Toulouse, Toulouse, France. lorenzo.scipioni@inserm.fr.ORCID http://orcid.org/0000-0003-2980-1912
Giulia Tedeschi *Centre de Recherche en Cancérologie de Toulouse, Toulouse, France.
Mariana X NavarroDepartment of Chemistry, University of California, Irvine, CA, USA.
Yunlong Y JiaDepartment of Developmental and Cell Biology, University of California, Irvine, CA, USA.ORCID http://orcid.org/0000-0001-7111-0520
Songning ZhuCentre de Recherche en Cancérologie de Toulouse, Toulouse, France.
Lila P HalbersDepartment of Pharmaceutical Sciences, University of California, Irvine, CA, USA.ORCID http://orcid.org/0009-0005-4684-3307
Melody Di BonaDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Scott X AtwoodDepartment of Developmental and Cell Biology, University of California, Irvine, CA, USA.ORCID http://orcid.org/0000-0001-7407-9792
Jennifer A PrescherDepartment of Chemistry, University of California, Irvine, CA, USA.ORCID http://orcid.org/0000-0002-9250-4702
Enrico GrattonDepartment of Biomedical Engineering, Laboratory for Fluorescence Dynamics, University of California, Irvine, Irvine, CA, USA.ORCID http://orcid.org/0000-0002-6450-7391
Michelle A DigmanDepartment of Biomedical Engineering, Laboratory for Fluorescence Dynamics, University of California, Irvine, Irvine, CA, USA. mdigman@uci.edu.ORCID http://orcid.org/0000-0003-4611-7100

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
UCI P30 Skin Center Systems Biology CoreP30AR075047 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI ANDERSEN, BOGI, GANESAN, ANAND K · 2019 to 2025
$5.1M
National Science Foundation (NSF) 1847005National Science Foundation (NSF) CBET2134916U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30CA062203U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) P30AR075047
6 · The paper itself

Abstract

Omics technologies such as genomics, transcriptomics, proteomics and metabolomics methods, have been instrumental in improving our understanding of complex biological systems by providing high-dimensional phenotypes of cell populations and single cells. Despite fast-paced advancements, these methods are limited in their ability to include a temporal dimension. Here, we introduce ESPRESSO (Environmental Sensor Phenotyping RElayed by Subcellular Structures and Organelles), a technique that provides single-cell, high-dimensional phenotyping resolved in space and time. ESPRESSO combines fluorescent labeling, advanced microscopy and image and data analysis methods to extract morphological and functional information from organelles at the single-cell level. We validate ESPRESSO's methodology and its application across numerous cellular systems for the analysis of cell type, stress response, differentiation and immune cell polarization. We show that ESPRESSO can correlate phenotype changes with gene expression, and demonstrate its applicability to 3D cultures, offering a path to improved spatially and temporally resolved biological exploration of cellular states.

Indexed as

GenomicsOrganellesSingle-Cell AnalysisAnimalsHumansMetabolomicsPhenotypeProteomics

Identifiers

What OpenQuestion holds

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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.