Evidence map›Paper›PMID 17113577›Full record

ArticleDevelopmental biology2007

Intrinsic differences among spatially distinct neural crest stem cells in terms of migratory properties, fate determination, and ability to colonize the enteric nervous system.

Jack T Mosher, Kelly J Yeager, Genevieve M Kruger, Nancy M Joseph, Mark E Hutchin, Andrzej A Dlugosz, Sean J Morrison

Abstract readComparative Study
In one paragraph

Article in Developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
  2. Article
  3. Neural crest-like stem cells for tissue regeneration.Stem cells translational medicine · 2021
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Jack T MosherDepartment of Internal Medicine, Center for Stem Cell Biology, Howard Hughes Medical Institute, 3435 Life Sciences Institute, 210 Washtenaw Avenue, Ann Arbor, MI 48109, USA.
Kelly J Yeager
Genevieve M Kruger
Nancy M Joseph
Mark E Hutchin
Andrzej A Dlugosz
Sean J Morrison
Howard Hughes Medical Institute · USUniversity of Michigan · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Scott Michael Schuetze · 1988 to 2026
$178.2M
MOLECULAR REGULATION OF HAIR FOLLICLE MORPHOGENESISR01AR045973 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DLUGOSZ, ANDRZEJ A. · 2000 to 2014
$4.8M
STEM CELLS IN PERIPHERAL NERVOUS SYSTEM DEVELOPMENTR01NS040750 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI MORRISON, SEAN J · 2001 to 2014
$3.6M
UNIVERSITY OF MICHIGAN MULTIPURPOSE ARTHRITIS CENTERP60AR020557 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GRUPPEN, LARRY D · 1986 to 2001
$2.9M
NCI NIH HHS CA 46592NCI NIH HHS P30 CA046592NIAMS NIH HHS AR 20557NIAMS NIH HHS R01 AR045973NINDS NIH HHS R01 NS040750NINDS NIH HHS R01 NS 40750
6 · The paper itself

Abstract

We have systematically examined the developmental potential of neural crest stem cells from the enteric nervous system (gut NCSCs) in vivo to evaluate their potential use in cellular therapy for Hirschsprung disease and to assess differences in the properties of postmigratory NCSCs from different regions of the developing peripheral nervous system (PNS). When transplanted into developing chicks, flow-cytometrically purified gut NCSCs and sciatic nerve NCSCs exhibited intrinsic differences in migratory potential and neurogenic capacity throughout the developing PNS. Most strikingly, gut NCSCs migrated into the developing gut and formed enteric neurons, while sciatic nerve NCSCs failed to migrate into the gut or to make enteric neurons, even when transplanted into the gut wall. Enteric potential is therefore not a general property of NCSCs. Gut NCSCs also formed cholinergic neurons in parasympathetic ganglia, but rarely formed noradrenergic sympathetic neurons or sensory neurons. Supporting the potential for autologous transplants in Hirschsprung disease, we observed that Endothelin receptor B (Ednrb)-deficient gut NCSCs engrafted and formed neurons as efficiently in the Ednrb-deficient hindgut as did wild-type NCSCs. These results demonstrate intrinsic differences in the migratory properties and developmental potentials of regionally distinct NCSCs, indicating that it is critical to match the physiological properties of neural stem cells to the goals of proposed cell therapies.

Indexed as

AnimalsCell- and Tissue-Based TherapyCell DifferentiationCell LineageCell MovementCells, CulturedChick EmbryoDNA PrimersEmbryonic Stem CellsEnteric Nervous SystemFemaleGastrointestinal TractHirschsprung DiseaseImmunohistochemistryIn Situ HybridizationMelanocytesDNA PrimersReceptors, Endothelin

Identifiers

PMID17113577
PMCPMC1910607
OpenAlexW2007365604

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.