Evidence map›Paper›PMID 17638088›Full record

ArticleJournal of muscle research and cell motility2007

Smooth muscle persists in the muscularis externa of developing and adult mouse esophagus.

Mark Rishniw, Pat W Fisher, Robert M Doran, Eric Meadows, William H Klein, Michael I Kotlikoff

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of muscle research and cell motility, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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  8. Review
  9. Review
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  12. Molecular aspects of esophageal development.Annals of the New York Academy of Sciences · 2011
    Article
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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

6 authors at 2 institutions in 1 country.

Mark RishniwDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, T4 018 VRT, Box 11, Ithaca, NY 14853, USA.
Pat W Fisher
Robert M Doran
Eric Meadows
William H Klein
Michael I Kotlikoff
Cornell University · USThe University of Texas MD Anderson Cancer Center · US

Funding

TRAINING PROGRAM IN COMPARATIVE MEDICINET32RR007059 · NCRR · CORNELL UNIVERSITY ITHACA · PI PARKER, JOHN S · 1995 to 2011
$4.2M
Transgenic Mice- Recomb., Fate-Mapping,and Ca2+signalingR01DK065992 · NIDDK · CORNELL UNIVERSITY ITHACA · PI KOTLIKOFF, MICHAEL I. · 2004 to 2008
$1.9M
NCRR NIH HHS T32RR07059-09NIDDK NIH HHS R01 DK065992
6 · The paper itself

Abstract

Following initial patterning as differentiated smooth muscle (SM) cells, the muscularis externa of the murine esophagus is replaced by skeletal muscle, but the mechanism underlying this process is controversial. The hypothesis that committed SM cells transdifferentiate into striated muscle is not consistent with fate mapping studies. Similarly, apoptosis does not fully explain the process. Using immunohistochemical techniques and transgenic mice that express eGFP and Cre-recombinase exclusively in SM, we have identified a population of remnant SM cells that persist throughout the developing and mature murine esophagus. These cells display an atypical phenotype, are not associated with microvasculature, but are often apposed to cKit positive, interstitial cells of Cajal. The absolute length of the SM component of the developing esophagus remains constant during a period when total esophageal length increases 4-fold, resulting in a small maintained distal segment of smooth muscle. Esophageal SM cells fail to express myogenin during development, and striated muscle cell precursors expressing myogenin fail to express specific SM cell markers, indicating that they did not transdifferentiate from SM cells. Moreover, smooth muscle-specific myogenin inactivation has no effect on esophageal skeletal myogenesis. Taken together, our results provide an alternative hypothesis regarding the fate of SM cells in the developing murine esophagus, which does not invoke apoptosis or transdifferentiation.

Indexed as

ActinsAgingAnimalsAnimals, NewbornApoptosisBody PatterningCell DifferentiationCell LineageCell ShapeEsophagusFemaleGreen Fluorescent ProteinsImmunohistochemistryIntegrasesMaleMiceActa2 protein, ratActinsCre recombinaseGreen Fluorescent ProteinsIntegrasesMyogenin

Identifiers

PMID17638088
OpenAlexW2065376086

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.