Evidence map›Paper›PMID 36300492›Full record

ArticleDevelopment (Cambridge, England)2022

In toto imaging of early enteric nervous system development reveals that gut colonization is tied to proliferation downstream of Ret.

Phillip A Baker, Rodrigo Ibarra-García-Padilla, Akshaya Venkatesh, Eileen W Singleton, Rosa A Uribe

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Whole-Gut Spatial Genomic Analysis Reveals Molecular Regionalization of the Differentiating Zebrafish Enteric Nervous System.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  3. BMP signaling pathway member expression is enriched in enteric neural progenitors and required for zebrafish enteric nervous system development.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Hirschsprung disease.Nature reviews. Disease primers · 2023
    Review
  9. 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

5 authors at 1 institution in 1 country.

Phillip A BakerBioSciences Department, Rice University, Houston, TX 77005, USA.
Rodrigo Ibarra-García-PadillaBioSciences Department, Rice University, Houston, TX 77005, USA.
Akshaya VenkateshBioSciences Department, Rice University, Houston, TX 77005, USA.
Eileen W SingletonBioSciences Department, Rice University, Houston, TX 77005, USA.
Rosa A UribeBioSciences Department, Rice University, Houston, TX 77005, USA.ORCID 0000-0002-0427-4493
Rice University · US

Funding

Genetic and extrinsic mechanisms governing early enteric nervous system developmentR01DK124804 · NIDDK · RICE UNIVERSITY · PI URIBE, ROSA A · 2021 to 2025
$1.9M
National Science Foundation 1942019NIDDK NIH HHS R01 DK124804NIH HHS DK124804
6 · The paper itself

Abstract

The enteric nervous system is a vast intrinsic network of neurons and glia within the gastrointestinal tract and is largely derived from enteric neural crest cells (ENCCs) that emigrate into the gut during vertebrate embryonic development. Study of ENCC migration dynamics and their genetic regulators provides great insights into fundamentals of collective cell migration and nervous system formation, and these are pertinent subjects for study due to their relevance to the human congenital disease Hirschsprung disease (HSCR). For the first time, we performed in toto gut imaging and single-cell generation tracing of ENCC migration in wild type and a novel ret heterozygous background zebrafish (retwmr1/+) to gain insight into ENCC dynamics in vivo. We observed that retwmr1/+ zebrafish produced fewer ENCCs localized along the gut, and these ENCCs failed to reach the hindgut, resulting in HSCR-like phenotypes. Specifically, we observed a proliferation-dependent migration mechanism, where cell divisions were associated with inter-cell distances and migration speed. Lastly, we detected a premature neuronal differentiation gene expression signature in retwmr1/+ ENCCs. These results suggest that Ret signaling may regulate maintenance of a stem state in ENCCs.

Indexed as

Enteric Nervous SystemHirschsprung DiseaseAnimalsCell DivisionCell MovementCell ProliferationHumansIntestinesNeural CrestProto-Oncogene Proteins c-retZebrafishProto-Oncogene Proteins c-retRET protein, humanDifferentiationEnteric nervous systemEnteric neural crestProliferationRetZebrafish

Identifiers

PMID36300492
PMCPMC9686996
OpenAlexW4307426117

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.