Evidence map›Paper›PMID 27181744›Full record

ArticleScientific reports2016

Notch signalling regulates asymmetric division and inter-conversion between lgr5 and bmi1 expressing intestinal stem cells.

Tara Srinivasan, Elaine Bich Than, Pengcheng Bu, Kuei-Ling Tung, Kai-Yuan Chen, Leonard Augenlicht, Steven M Lipkin, Xiling Shen

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Rewinding the clock: mechanisms of dedifferentiation.Current opinion in genetics & development · 2025
    Review
  8. Intestinal organ chips for disease modelling and personalized medicine.Nature reviews. Gastroenterology & hepatology · 2024
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Nutrients · 2023
    Article
  14. Review
  15. Review
  16. Glycans that regulate Notch signaling in the intestine.Biochemical Society transactions · 2022
    Review
  17. Review
  18. Article
  19. Asymmetric Cell Division and Tumor Heterogeneity.Frontiers in cell and developmental biology · 2022
    Review
  20. LGR5, HES1 and ATOH1 in Young Rectal Cancer Patients in Egyptian.Asian Pacific journal of cancer prevention : APJCP · 2021
    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

8 authors.

Tara SrinivasanDepartment of Biomedical Engineering, Cornell University, Ithaca, New York, 14853, USA.
Elaine Bich ThanDepartments of Medicine, Surgery and Pathology, Weill Cornell Medical College, New York City, New York, 10021, USA.
Pengcheng BuDepartment of Biomedical Engineering, Cornell University, Ithaca, New York, 14853, USA.
Kuei-Ling TungDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, New York, 14853, USA.
Kai-Yuan ChenDepartment of Biomedical Engineering, Cornell University, Ithaca, New York, 14853, USA.
Leonard AugenlichtDepartment of Oncology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, 10461 USA.
Steven M LipkinDepartments of Medicine, Surgery and Pathology, Weill Cornell Medical College, New York City, New York, 10021, USA.
Xiling ShenDepartment of Biomedical Engineering, Cornell University, Ithaca, New York, 14853, USA.

Funding

University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
Multi-scale modeling of asymmetric cell divisionR01GM095990 · NIGMS · CORNELL UNIVERSITY · PI SHEN, XILING · 2011 to 2015
$1.5M
Robustness of the Intestinal Stem Cell NicheR01GM114254 · NIGMS · DUKE UNIVERSITY · PI SHEN, XILING · 2015 to 2017
$918k
NCATS NIH HHS UL1 TR001414NIGMS NIH HHS R01 GM095990NIGMS NIH HHS R01 GM114254
6 · The paper itself

Abstract

Rapidly cycling LGR5+ intestinal stem cells (ISCs) located at the base of crypts are the primary driver of regeneration. Additionally, BMI1 expression is correlated with a slow cycling pool of ISCs located at +4 position. While previous reports have shown interconversion between these two populations following tissue injury, we provide evidence that NOTCH signaling regulates the balance between these two populations and promotes asymmetric division as a mechanism for interconversion in the mouse intestine. In both in vitro and in vivo models, NOTCH suppression reduces the ratio of BMI1+/LGR5+ ISCs while NOTCH stimulation increases this ratio. Furthermore, NOTCH signaling can activate asymmetric division after intestinal inflammation. Overall, these data provide insights into ISC plasticity, demonstrating a direct interconversion mechanism between slow- and fast-cycling ISCs.

Indexed as

Adult Stem CellsAnimalsCell DivisionCell PlasticityCells, CulturedCell TransdifferentiationIntestinesMiceMice, 129 StrainMice, Inbred C57BLMice, TransgenicPolycomb Repressive Complex 1Proto-Oncogene ProteinsReceptors, G-Protein-CoupledReceptors, NotchRegenerationBmi1 protein, mouseLgr5 protein, mousePolycomb Repressive Complex 1Proto-Oncogene ProteinsReceptors, G-Protein-CoupledReceptors, Notch

Identifiers

PMID27181744
PMCPMC4867651

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.