Evidence map›Paper›PMID 27881402›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2017

Maturity and age influence chief cell ability to transdifferentiate into metaplasia.

Victoria G Weis, Christine P Petersen, Jared A Weis, Anne R Meyer, Eunyoung Choi, Jason C Mills, James R Goldenring

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2017. 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
4.4field-weighted citation impact, top 6% 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, 36 citations in OpenAlex.

  1. Review
  2. Review
  3. Highlights of how single-cell analyses are illuminating differentiation and disease in the gastric corpus.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Review
  4. Review
  5. Review
  6. Review
  7. Cell plasticity in regeneration in the stomach and beyond.Current opinion in genetics & development · 2022
    Review
  8. The immune microenvironment in gastric adenocarcinoma.Nature reviews. Gastroenterology & hepatology · 2022
    Review
  9. Article
  10. Review
  11. ELAPOR1 is a secretory granule maturation-promoting factor that is lost during paligenosis.American journal of physiology. Gastrointestinal and liver physiology · 2022
    Article
  12. Article
  13. Review
  14. Human placental-derived stem cell therapy ameliorates experimental necrotizing enterocolitis.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Decrease in MiR-148a Expression During Initiation of Chief Cell Transdifferentiation.Cellular and molecular gastroenterology and hepatology · 2020
    Article
  19. Premalignant lesions and gastric cancer: Current understanding.World journal of gastrointestinal oncology · 2019
    Review
  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 3 institutions in 1 country.

Victoria G WeisSection of Surgical Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
Christine P PetersenNashville Veterans Affairs Medical Center, Nashville, Tennessee.
Jared A WeisDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.
Anne R MeyerDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee.
Eunyoung ChoiNashville Veterans Affairs Medical Center, Nashville, Tennessee.
Jason C MillsDivision of Gastroenterology, Departments of Medicine, Pathology and Immunology, and Developmental Biology, Washington University, St. Louis, Missouri.ORCID 0000-0002-0402-4662
James R GoldenringNashville Veterans Affairs Medical Center, Nashville, Tennessee; jim.goldenring@vanderbilt.edu.
Vanderbilt University · USVanderbilt University Medical Center · USWashington University in St. Louis · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
TRAINING IN GASTROENTEROLOGYT32DK007673 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 1992 to 2026
$8.4M
TRAINING PROGRAM IN CELLULAR, BIOCHEMICAL, &MOLECULAR ST32GM008554 · NIGMS · VANDERBILT UNIVERSITY · PI PATTON, JAMES G. · 1995 to 2020
$7.4M
REGULATION OF ATROPHY-INDUCED PROGENITOR CELLS IN THE GASTRIC CORPUSR01DK094989 · NIDDK · WASHINGTON UNIVERSITY · PI Jason C Mills · 2012 to 2026
$6.1M
Induction and Evolution of Metaplasia in the StomachR01DK101332 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Eunyoung Choi, James Richard Goldenring · 2014 to 2026
$5.9M
MECHANISMS OF CHIEF CELL DEDIFFERENTIATIONR01DK105129 · NIDDK · WASHINGTON UNIVERSITY · PI Jason C Mills · 2015 to 2026
$5.4M
Mechanisms of Gastric Mucous Cell MetaplasiaR01DK071590 · NIDDK · VANDERBILT UNIVERSITY · PI GOLDENRING, JAMES RICHARD · 2008 to 2012
$2.2M
Innate immune cell regulation of metaplasia in the stomachF31DK117592 · NIDDK · VANDERBILT UNIVERSITY · PI MEYER, ANNE R. · 2018 to 2020
$66k
Inflammatory mediators promote the development of metaplasia in the stomachF31DK104600 · NIDDK · VANDERBILT UNIVERSITY · PI PETERSEN, CHRISTINE POPE · 2014 to 2015
$55k
Oxyntic Atrophy and Novel Gastric Lineages.I01BX000930 · VA · VETERANS HEALTH ADMINISTRATION · PI GOLDENRING, JAMES RICHARD · 2011 to 2025
–
BLRD VA I01 BX000930NCI NIH HHS P30 CA068485NIDDK NIH HHS F31 DK104600NIDDK NIH HHS F31 DK117592NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK071590NIDDK NIH HHS R01 DK094989NIDDK NIH HHS R01 DK101332NIDDK NIH HHS R01 DK105129NIDDK NIH HHS T32 DK007673NIGMS NIH HHS T32 GM008554
6 · The paper itself

Abstract

The plasticity of gastric chief cells is exemplified by their ability to transdifferentiate into spasmolytic polypeptide-expressing metaplasia (SPEM) after parietal cell loss. We sought to determine if chief cell maturity is a limiting factor in the capacity to transdifferentiate. Mist1 NEW & NOTEWORTHY: Previous investigations have indicated that spasmolytic polypeptide-expressing metaplasia (SPEM) in the stomach arises from transdifferentiation of chief cells. Nevertheless, the intrinsic properties of chief cells that influence transdifferentiation have been largely unknown. We now report that the ability to transdifferentiate into SPEM is impaired in chief cells that lack full functional maturation, and as chief cells age, they lose their ability to transdifferentiate. Thus chief cell plasticity is dependent on both cell age and maturation.

Indexed as

Age FactorsAnimalsBasic Helix-Loop-Helix ProteinsCell LineageCell ProliferationCell TransdifferentiationChief Cells, GastricGastric MucosaIntercellular Signaling Peptides and ProteinsMetaplasiaMiceMice, KnockoutParietal Cells, GastricPeptidesStomachBasic Helix-Loop-Helix ProteinsBhlha15 protein, mouseIntercellular Signaling Peptides and ProteinsPeptidesspasmolytic polypeptidelineage mappingMist1progenitor cellspasmolytic polypeptide-expressing metaplasiaSPEMtransdifferentiation

Identifiers

PMID27881402
PMCPMC5283902
OpenAlexW2551058804

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.