Evidence map›Paper›PMID 20107080›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

The timing and location of glial cell line-derived neurotrophic factor expression determine enteric nervous system structure and function.

Hongtao Wang, Inna Hughes, William Planer, Alexander Parsadanian, John R Grider, Bhupinder P S Vohra, Cynthia Keller-Peck, Robert O Heuckeroth

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 97 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Altered Esophageal Smooth Muscle Phenotype in Achalasia.Journal of neurogastroenterology and motility · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Development, Diversity, and Neurogenic Capacity of Enteric Glia.Frontiers in cell and developmental biology · 2021
    Review
  11. Review
  12. Review
  13. Article
  14. Glial ACells · 2020
    Article
  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

8 authors at 3 institutions in 1 country.

Hongtao WangDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Inna Hughes
William Planer
Alexander Parsadanian
John R Grider
Bhupinder P S Vohra
Cynthia Keller-Peck
Robert O Heuckeroth
Washington University in St. Louis · USNeurology, Inc · USVirginia Commonwealth University Medical Center · US

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
ROLE OF GUT PEPTIDES IN INTESTINAL PERISTALSISR01DK034153 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRIDER, JOHN R · 1987 to 2019
$5.5M
Neuronal control of intestinal motility in mutant miceR01DK064592 · NIDDK · WASHINGTON UNIVERSITY · PI HEUCKEROTH, ROBERT O · 2003 to 2007
$2.5M
RET LIGAND REGULATION OF INTESTINAL MOTILITYR01DK057038 · NIDDK · WASHINGTON UNIVERSITY · PI HEUCKEROTH, ROBERT O · 2000 to 2009
$2.0M
GDNF: EFFECTS ON NORMAL AND DEGENERATING MOTOR NEURONSR01NS042794 · NINDS · WASHINGTON UNIVERSITY · PI PARSADANIAN, ALEXANDER S · 2002 to 2006
$1.5M
NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30-DK52574NIDDK NIH HHS R01 DK034153NIDDK NIH HHS R01 DK057038NIDDK NIH HHS R01 DK064592NIDDK NIH HHS R01 DK34153NIDDK NIH HHS R01 DK57038NIDDK NIH HHS R01 DK6459201NINDS NIH HHS NS042794NINDS NIH HHS R01 NS042794
6 · The paper itself

Abstract

Ret signaling is critical for formation of the enteric nervous system (ENS) because Ret activation promotes ENS precursor survival, proliferation, and migration and provides trophic support for mature enteric neurons. Although these roles are well established, we now provide evidence that increasing levels of the Ret ligand glial cell line-derived neurotrophic factor (GDNF) in mice causes alterations in ENS structure and function that are critically dependent on the time and location of increased GDNF availability. This is demonstrated using two different strains of transgenic mice and by injecting newborn mice with GDNF. Furthermore, because different subclasses of ENS precursors withdraw from the cell cycle at different times during development, increases in GDNF at specific times alter the ratio of neuronal subclasses in the mature ENS. In addition, we confirm that esophageal neurons are GDNF responsive and demonstrate that the location of GDNF production influences neuronal process projection for NADPH diaphorase-expressing, but not acetylcholinesterase-, choline acetyltransferase-, or tryptophan hydroxylase-expressing, small bowel myenteric neurons. We further demonstrate that changes in GDNF availability influence intestinal function in vitro and in vivo. Thus, changes in GDNF expression can create a wide variety of alterations in ENS structure and function and may in part contribute to human motility disorders.

Indexed as

AnimalsCell CycleCell DifferentiationCell ProliferationEnteric Nervous SystemEsophagusGastrointestinal MotilityGene Expression Regulation, DevelopmentalGlial Cell Line-Derived Neurotrophic FactorMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicMyenteric PlexusNADPH DehydrogenaseNeuritesGlial Cell Line-Derived Neurotrophic FactorNADPH DehydrogenaseProto-Oncogene Proteins c-ret

Identifiers

PMID20107080
PMCPMC2836725
OpenAlexW2066250445

What OpenQuestion holds

Textmetadata
LicenceTDM
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.