Evidence map›Paper›PMID 39592623›Full record

ArticleNature communications2024

Quantitative determination of the spatial distribution of components in single cells with CellDetail.

Tanja Schuster, Amanda Amoah, Angelika Vollmer, Gina Marka, Julian Niemann, Mehmet Saçma, Vadim Sakk, Karin Soller, Mona Vogel, Ani Grigoryan and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. 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

14 authors.

Tanja SchusterInstitute of Molecular Medicine, Ulm University, Ulm, Germany. tanja.schuster@uni-ulm.de.ORCID 0009-0000-2691-4570
Amanda AmoahInstitute of Molecular Medicine, Ulm University, Ulm, Germany.ORCID 0000-0002-1267-4091
Angelika VollmerInstitute of Molecular Medicine, Ulm University, Ulm, Germany.
Gina MarkaInstitute of Molecular Medicine, Ulm University, Ulm, Germany.
Julian NiemannInstitute of Molecular Medicine, Ulm University, Ulm, Germany.
Mehmet SaçmaInstitute of Molecular Medicine, Ulm University, Ulm, Germany.ORCID 0000-0003-3450-674X
Vadim SakkInstitute of Molecular Medicine, Ulm University, Ulm, Germany.
Karin SollerInstitute of Molecular Medicine, Ulm University, Ulm, Germany.
Mona VogelInstitute of Molecular Medicine, Ulm University, Ulm, Germany.
Ani GrigoryanInstitute of Molecular Medicine, Ulm University, Ulm, Germany.ORCID 0000-0003-2757-7021
Meinhard WlaschekDepartment of Dermatology and Allergic Diseases, Ulm University, Ulm, Germany.
Karin Scharffetter-KochanekDepartment of Dermatology and Allergic Diseases, Ulm University, Ulm, Germany.ORCID 0000-0002-9655-685X
Medhanie MulawUnit for Single-Cell Genomics, Ulm University, Ulm, Germany.ORCID 0000-0002-2501-6952
Hartmut GeigerInstitute of Molecular Medicine, Ulm University, Ulm, Germany. hartmut.geiger@uni-ulm.de.ORCID 0000-0002-5794-5430

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) FOR 2674Deutsche Forschungsgemeinschaft (German Research Foundation) SFB 1506
6 · The paper itself

Abstract

The distribution of biomolecules within cells changes upon aging and diseases. To quantitatively determine the spatial distribution of components inside cells, we built the user-friendly open-source 3D-cell-image analysis platform Cell Detection and Analysis of Intensity Lounge (CellDetail). The algorithm within CellDetail is based on the concept of the dipole moment. CellDetail provides quantitative values for the distribution of the polarity proteins Cdc42 and Tubulin in young and aged hematopoietic stem cells (HSCs). Septin proteins form networks within cells that are critical for cell compartmentalization. We uncover a reduced level of organization of the Septin network within aged HSCs and within senescent human fibroblasts. Changes in the Septin network structure might therefore be a common feature of aging. The level of organization of the network of Septin proteins in aged HSCs can be restored to a youthful level by pharmacological attenuation of the activity of the small RhoGTPase Cdc42.

Indexed as

Algorithmscdc42 GTP-Binding ProteinFibroblastsHematopoietic Stem CellsSeptinsSingle-Cell AnalysisAnimalsCellular SenescenceHumansImaging, Three-DimensionalMiceTubulincdc42 GTP-Binding ProteinCDC42 protein, humanSeptinsTubulin

Identifiers

PMID39592623
PMCPMC11599593

What OpenQuestion holds

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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.