Evidence map›Paper›PMID 28982714›Full record

ArticleJournal of cell science2017

Interkinetic nuclear migration and basal tethering facilitates post-mitotic daughter separation in intestinal organoids.

Thomas D Carroll, Alistair J Langlands, James M Osborne, Ian P Newton, Paul L Appleton, Inke Näthke

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Capturing Stem Cell Behavior Using Intravital and Live Cell Microscopy.Cold Spring Harbor perspectives in biology · 2020
    Review
  11. Article
  12. Article
  13. Intestinal renewal across the animal kingdom: comparing stem cell activity in mouse and Drosophila.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Review
  14. 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

6 authors at 2 institutions in 2 countries.

Thomas D CarrollCell & Developmental Biology, University of Dundee, Dundee DD1 5EH, UK.
Alistair J LanglandsCell & Developmental Biology, University of Dundee, Dundee DD1 5EH, UK.
James M OsborneSchool of Mathematics and Statistics, University of Melbourne, Melbourne 3010, Australia.
Ian P NewtonCell & Developmental Biology, University of Dundee, Dundee DD1 5EH, UK.
Paul L AppletonDundee Imaging Facility, University of Dundee, Dundee DD1 5EH, UK.
Inke NäthkeCell & Developmental Biology, University of Dundee, Dundee DD1 5EH, UK i.s.nathke@dundee.ac.uk.ORCID http://orcid.org/0000-0003-2420-4385
University of Dundee · GBThe University of Melbourne · AU

Funding

Cancer Research UK 11243Wellcome Trust 205023/Z/16/Z
6 · The paper itself

Abstract

Homeostasis of renewing tissues requires balanced proliferation, differentiation and movement. This is particularly important in the intestinal epithelium where lineage tracing suggests that stochastic differentiation choices are intricately coupled to the position of a cell relative to a niche. To determine how position is achieved, we followed proliferating cells in intestinal organoids and discovered that the behaviour of mitotic sisters predicted long-term positioning. We found that, normally, 70% of sisters remain neighbours, while 30% lose contact and separate after cytokinesis. These post-mitotic placements predict longer term differences in positions assumed by sisters: adjacent sisters reach similar positions over time; in a pair of separating sisters, one remains close to its birthplace while the other is displaced upward. Computationally modelling crypt dynamics confirmed that post-mitotic separation leads to sisters reaching different compartments. We show that interkinetic nuclear migration, cell size and asymmetric tethering by a process extending from the basal side of cells contribute to separations. These processes are altered in adenomatous polyposis coli (

Indexed as

AnimalsBiological TransportCell AdhesionCell NucleusHumansIntestinal MucosaKineticsMice, Inbred C57BLMice, TransgenicMitosisOrganoidsTissue Culture TechniquesAdenomatous polyposis coliInterkinetic nuclear migrationIntestinal epitheliumMitosis

Identifiers

PMID28982714
PMCPMC5702049
OpenAlexW2761405906

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.