Evidence map›Paper›PMID 21270052›Full record

ArticleDevelopment (Cambridge, England)2011

Stage-specific signaling through TGFβ family members and WNT regulates patterning and pancreatic specification of human pluripotent stem cells.

M Cristina Nostro, Farida Sarangi, Shinichiro Ogawa, Audrey Holtzinger, Barbara Corneo, Xueling Li, Suzanne J Micallef, In-Hyun Park, Christina Basford, Michael B Wheeler and 4 more

Erratum issuedAbstract read
In one paragraph

Article in Development (Cambridge, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 237 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
237citing papers in PubMed, 1 pooled it
40.4field-weighted citation impact, top 1% 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

237 citing papers in PubMed, 1 synthesis or guideline pooled it, 384 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. GRP94 is indispensable for definitive endoderm specification of human induced pluripotent stem cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Current Organoid Culture Systems in Pancreatic Cancer.Current topics in medicinal chemistry · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Stem Cell Therapy for the Management of Type 1 Diabetes: Advances and Perspectives.Endocrine, metabolic & immune disorders drug targets · 2024
    Review
  20. Article

177 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
  • Erratum issued
5 · Who and what money

Authors and funding

14 authors at 6 institutions in 3 countries.

M Cristina NostroMcEwen Centre for Regenerative Medicine, University Health Network, Toronto, Ontario, Canada.
Farida Sarangi
Shinichiro Ogawa
Audrey Holtzinger
Barbara Corneo
Xueling Li
Suzanne J Micallef
In-Hyun Park
Christina Basford
Michael B Wheeler
George Q Daley
Andrew G Elefanty
Edouard G Stanley
Gordon Keller
University Health Network · CAMonash University · AUUniversity of Toronto · CADana-Farber Cancer Institute · USNeural Stem Cell Institute · USYale Cancer Center · US

Funding

Endoderm Induction and Pancreatic Specification from ES*U01DK072513 · NIDDK · UNIVERSITY HEALTH NETWORK · PI KELLER, GORDON · 2005 to 2009
$3.8M
NIDDK NIH HHS U01 DK072513NIDDK NIH HHS U01-DK072513
6 · The paper itself

Abstract

The generation of insulin-producing β-cells from human pluripotent stem cells is dependent on efficient endoderm induction and appropriate patterning and specification of this germ layer to a pancreatic fate. In this study, we elucidated the temporal requirements for TGFβ family members and canonical WNT signaling at these developmental stages and show that the duration of nodal/activin A signaling plays a pivotal role in establishing an appropriate definitive endoderm population for specification to the pancreatic lineage. WNT signaling was found to induce a posterior endoderm fate and at optimal concentrations enhanced the development of pancreatic lineage cells. Inhibition of the BMP signaling pathway at specific stages was essential for the generation of insulin-expressing cells and the extent of BMP inhibition required varied widely among the cell lines tested. Optimal stage-specific manipulation of these pathways resulted in a striking 250-fold increase in the levels of insulin expression and yielded populations containing up to 25% C-peptide+ cells.

Indexed as

ActivinsBody PatterningBone Morphogenetic ProteinsCell LineCell LineageC-PeptideEndodermHumansInsulinInsulin-Secreting CellsPancreasPluripotent Stem CellsSignal TransductionTransforming Growth Factor betaWnt Proteinsactivin AActivinsBone Morphogenetic ProteinsC-PeptideInsulinTransforming Growth Factor betaWnt Proteins

Identifiers

PMID21270052
PMCPMC3035090
OpenAlexW2170781656

What OpenQuestion holds

Textmetadata
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.