Evidence map›Paper›PMID 38110222›Full record

ArticleLife science alliance2024

Single-cell time series analysis reveals the dynamics of HSPC response to inflammation.

Brigitte J Bouman, Yasmin Demerdash, Shubhankar Sood, Florian Grünschläger, Franziska Pilz, Abdul R Itani, Andrea Kuck, Valérie Marot-Lassauzaie, Simon Haas, Laleh Haghverdi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Variational inference of single cell time series.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Review
  9. Microheterogeneity in the Kinetics and Sex-Specific Response to Type I IFN.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  10. 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

11 authors at 2 institutions in 1 country.

Brigitte J BoumanBerlin Institute for Medical Systems Biology, Max Delbrück Center in the Helmholtz Association, Berlin, Germany.
Yasmin DemerdashDivision Inflammatory Stress in Stem Cells, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Shubhankar SoodDivision Inflammatory Stress in Stem Cells, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Florian GrünschlägerHeidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGMBH), Heidelberg, Germany.
Franziska PilzDivision Inflammatory Stress in Stem Cells, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Abdul R ItaniDivision Inflammatory Stress in Stem Cells, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0001-7608-822X
Andrea KuckDivision Inflammatory Stress in Stem Cells, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Valérie Marot-LassauzaieBerlin Institute for Medical Systems Biology, Max Delbrück Center in the Helmholtz Association, Berlin, Germany.ORCID 0000-0002-8362-9634
Simon HaasBerlin Institute for Medical Systems Biology, Max Delbrück Center in the Helmholtz Association, Berlin, Germany.
Laleh HaghverdiBerlin Institute for Medical Systems Biology, Max Delbrück Center in the Helmholtz Association, Berlin, Germany Laleh.Haghverdi@mdc-berlin.de.ORCID 0000-0001-9280-9170
Marieke Ag EssersDivision Inflammatory Stress in Stem Cells, German Cancer Research Center (DKFZ), Heidelberg, Germany m.essers@dkfz-heidelberg.de.ORCID 0000-0003-3117-1809
German Cancer Research Center · DEMax Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic stem and progenitor cells (HSPCs) are known to respond to acute inflammation; however, little is understood about the dynamics and heterogeneity of these stress responses in HSPCs. Here, we performed single-cell sequencing during the sensing, response, and recovery phases of the inflammatory response of HSPCs to treatment (a total of 10,046 cells from four time points spanning the first 72 h of response) with the pro-inflammatory cytokine IFNα to investigate the HSPCs' dynamic changes during acute inflammation. We developed the essential novel computational approaches to process and analyze the resulting single-cell time series dataset. This includes an unbiased cell type annotation and abundance analysis post inflammation, tools for identification of global and cell type-specific responding genes, and a semi-supervised linear regression approach for response pseudotime reconstruction. We discovered a variety of different gene responses of the HSPCs to the treatment. Interestingly, we were able to associate a global reduced myeloid differentiation program and a locally enhanced pyroptosis activity with reduced myeloid progenitor and differentiated cells after IFNα treatment. Altogether, the single-cell time series analyses have allowed us to unbiasedly study the heterogeneous and dynamic impact of IFNα on the HSPCs.

Indexed as

HematopoiesisHematopoietic Stem CellsCell DifferentiationHumansInflammationTime Factors

Identifiers

PMID38110222
PMCPMC10728485
OpenAlexW4389889826

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.