Evidence map›Paper›PMID 30443337›Full record

ArticleInterface focus2018

Haematopoietic stem cells: entropic landscapes of differentiation.

K Wiesner, J Teles, M Hartnor, C Peterson

Abstract read
In one paragraph

Article in Interface focus, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. T-cell commitment inheritance-an agent-based multi-scale model.NPJ systems biology and applications · 2024
    Article
  5. T-cell commitment inheritance - an agent-based multi-scale model.bioRxiv : the preprint server for biology · 2023
    Article
  6. The Growing Liberality Observed in Primary Animal and Plant Cultures is Common to the Social Amoeba.Journal of bioinformatics and systems biology : Open access · 2023
    Article
  7. Journal of biotechnology and biomedicine · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

4 authors.

K WiesnerSchool of Mathematics, University of Bristol, Bristol BS8 1TW, UK.ORCID 0000-0003-2944-1988
J TelesComputational Biology and Biological Physics, Department of Astronomy and Theoretical Physics, Lund University, Lund 223 62, Sweden.
M HartnorComputational Biology and Biological Physics, Department of Astronomy and Theoretical Physics, Lund University, Lund 223 62, Sweden.
C PetersonComputational Biology and Biological Physics, Department of Astronomy and Theoretical Physics, Lund University, Lund 223 62, Sweden.ORCID 0000-0001-7362-2191

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The metaphor of a potential epigenetic differentiation landscape broadly suggests that during differentiation a stem cell approaches a stable equilibrium state from a higher free energy towards a stable equilibrium state which represents the final cell type. It has been conjectured that there is an analogy to the concept of entropy in statistical mechanics. In this context, in the undifferentiated state, the entropy would be large since fewer constraints exist on the gene expression programmes of the cell. As differentiation progresses, gene expression programmes become more and more constrained and thus the entropy would be expected to decrease. In order to assess these predictions, we compute the Shannon entropy for time-resolved single-cell gene expression data in two different experimental set-ups of haematopoietic differentiation. We find that the behaviour of this entropy measure is in contrast to these predictions. In particular, we find that the Shannon entropy is not a decreasing function of developmental pseudo-time but instead it increases towards the time point of commitment before decreasing again. This behaviour is consistent with an increase in gene expression disorder observed in populations sampled at the time point of commitment. Single cells in these populations exhibit different combinations of regulator activity that suggest the presence of multiple configurations of a potential differentiation network as a result of multiple entry points into the committed state.

Indexed as

entropyShannon information theorystem cell differentiation

Identifiers

PMID30443337
PMCPMC6227807

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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.