Evidence map›Paper›PMID 39215170›Full record

ArticleCommunications biology2024

Cell sorting based on pulse shapes from angle resolved detection of scattered light.

Daniel Kage, Andrej Eirich, Kerstin Heinrich, Jenny Kirsch, Jan Popien, Alexander Wolf, Konrad V Volkmann, Hyun-Dong Chang, Toralf Kaiser

Abstract read
In one paragraph

Article in Communications biology, 2024. 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
–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

2 citing papers in PubMed.

  1. Leukocyte dynamics inFrontiers in immunology · 2025
    Article
  2. 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.

Daniel KageGerman Rheumatology Research Center (DRFZ) - Flow Cytometry Core Facility, Charitéplatz 1 (Virchowweg 12), 10117, Berlin, Germany.ORCID 0000-0003-0087-0359
Andrej EirichAPE Angewandte Physik und Elektronik GmbH, Plauener Straße 163-165 / Haus N, 13053, Berlin, Germany.
Kerstin HeinrichGerman Rheumatology Research Center (DRFZ) - Flow Cytometry Core Facility, Charitéplatz 1 (Virchowweg 12), 10117, Berlin, Germany.
Jenny KirschGerman Rheumatology Research Center (DRFZ) - Flow Cytometry Core Facility, Charitéplatz 1 (Virchowweg 12), 10117, Berlin, Germany.
Jan PopienAPE Angewandte Physik und Elektronik GmbH, Plauener Straße 163-165 / Haus N, 13053, Berlin, Germany.
Alexander WolfGerman Rheumatology Research Center (DRFZ) - Flow Cytometry Core Facility, Charitéplatz 1 (Virchowweg 12), 10117, Berlin, Germany.
Konrad V VolkmannAPE Angewandte Physik und Elektronik GmbH, Plauener Straße 163-165 / Haus N, 13053, Berlin, Germany.
Hyun-Dong ChangGerman Rheumatology Research Center (DRFZ) - Flow Cytometry Core Facility, Charitéplatz 1 (Virchowweg 12), 10117, Berlin, Germany.ORCID 0000-0002-7341-4533
Toralf KaiserGerman Rheumatology Research Center (DRFZ) - Flow Cytometry Core Facility, Charitéplatz 1 (Virchowweg 12), 10117, Berlin, Germany. kaiser@drfz.de.ORCID 0000-0002-4685-5851

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 491069896
6 · The paper itself

Abstract

Flow cytometry is a key technology for the analysis and sorting of cells or particles at high throughput. Conventional and current flow cytometry is primarily based on fluorescent stains to detect the cells of interest. However, such stains also have disadvantages, as their effect on cells must be carefully tested to avoid effects on the results of the experiments. Alternative approaches using imaging or other label-free techniques often require highly sophisticated setups, are commonly limited in resolution, and produce challenging amounts of data. Our technology exploits scattered light instead. The custom-built flow cytometry setup comprises a fiber array in forward scatter detection for angular resolution and captures the whole pulse shape with advanced signal processing. Thereby this setup enables cell analysis and sorting purely based on scattered light signals without the need for fluorescent labels. We demonstrate the feasibility of this cell sorting technology by sorting cell lines for their cell cycle stages based on scattered light. Furthermore, we demonstrate the ability to classify human peripheral blood T- and B-cell subsets.

Indexed as

Flow CytometryLightB-LymphocytesCell SeparationHumansScattering, Radiation

Identifiers

PMID39215170
PMCPMC11364749

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.