Evidence map›Paper›PMID 18537141›Full record

ArticleThe Journal of comparative neurology2008

Bone morphogenetic protein regulation of enteric neuronal phenotypic diversity: relationship to timing of cell cycle exit.

Alcmène Chalazonitis, Tuan D Pham, Zhishan Li, Daniel Roman, Udayan Guha, William Gomes, Lixin Kan, John A Kessler, Michael D Gershon

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of comparative neurology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
9.5field-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

65 citing papers in PubMed, 122 citations in OpenAlex.

  1. Article
  2. Review
  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
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  11. The Shaggy Dog Story of Enteric Signaling: Serotonin, a Molecular Megillah.Advances in experimental medicine and biology · 2022
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5 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 1 country.

Alcmène ChalazonitisDeparment of Pathology & Cell Biology, Columbia University, New York, New York 10032, USA. ac83@columbia.edu
Tuan D Pham
Zhishan Li
Daniel Roman
Udayan Guha
William Gomes
Lixin Kan
John A Kessler
Michael D Gershon
Columbia University · USNorthwestern University · USMemorial Sloan Kettering Cancer Center · USMontefiore Medical Center · US

Funding

MICROENVIRONMENT IN ENTERIC NEURON DEVELOPMENTR01NS015547 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI GERSHON, MICHAEL D, MARGOLIS, KARA GROSS · 1985 to 2022
$7.2M
REGULATION OF NEUROTRANSMITTER METABOLISMR01NS020778 · NINDS · YESHIVA UNIVERSITY · PI KESSLER, JOHN A · 1985 to 2014
$4.6M
MECHANISMS GOVERNING NEURONAL DEVELOPMENTR01NS020013 · NINDS · YESHIVA UNIVERSITY · PI KESSLER, JOHN A · 1985 to 2013
$4.1M
Regulatory Molecules in Enteric Nervous SystemR01DK058056 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHALAZONITIS-GREENE, ALCMENE · 2002 to 2006
$1.2M
NIDDK NIH HHS DK58056NIDDK NIH HHS R01 DK058056NINDS NIH HHS NS15547NINDS NIH HHS NS 20013NINDS NIH HHS NS 20778NINDS NIH HHS R01 NS015547NINDS NIH HHS R01 NS020013NINDS NIH HHS R01 NS020778
6 · The paper itself

Abstract

The effects of bone morphogenetic protein (BMP) signaling on enteric neuron development were examined in transgenic mice overexpressing either the BMP inhibitor, noggin, or BMP4 under control of the neuron specific enolase (NSE) promoter. Noggin antagonism of BMP signaling increased total numbers of enteric neurons and those of subpopulations derived from precursors that exit the cell cycle early in neurogenesis (serotonin, calretinin, calbindin). In contrast, noggin overexpression decreased numbers of neurons derived from precursors that exit the cell cycle late (gamma-aminobutyric acid, tyrosine hydroxylase [TH], dopamine transporter, calcitonin gene-related peptide, TrkC). The numbers of TH- and TrkC-expressing neurons were increased by overexpression of BMP4. These observations are consistent with the idea that phenotypic expression in the enteric nervous system (ENS) is determined, in part, by the number of proliferative divisions neuronal precursors undergo before their terminal mitosis. BMP signaling may thus regulate enteric neuronal phenotypic diversity by promoting the exit of precursors from the cell cycle. BMP2 increased the numbers of TH- and TrkC-expressing neurons developing in vitro from immunoselected enteric crest-derived precursors; BMP signaling may thus also specify or promote the development of dopaminergic TrkC/NT-3-dependent neurons. The developmental defects in the ENS of noggin-overexpressing mice caused a relatively mild disturbance of motility (irregular rapid transit and increased stool frequency, weight, and water content). Although the function of the gut thus displays a remarkable tolerance for ENS defects, subtle functional abnormalities in motility or secretion may arise when ENS defects short of aganglionosis occur during development.

Indexed as

PhenotypeAmino Acid SequenceAnimalsBone Morphogenetic Protein 4Carrier ProteinsCell CountCell CycleCells, CulturedEnteric Nervous SystemFemaleGenetic VariationMaleMiceMice, TransgenicMolecular Sequence DataNeuronsBmp4 protein, mouseBone Morphogenetic Protein 4Carrier ProteinsNoggin Protein

Identifiers

PMID18537141
PMCPMC2592098
OpenAlexW2090379221

What OpenQuestion holds

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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.