Evidence map›Paper›PMID 8755542›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

Human fetal enterocytes in vitro: modulation of the phenotype by extracellular matrix.

I R Sanderson, R M Ezzell, M Kedinger, M Erlanger, Z X Xu, E Pringault, S Leon-Robine, D Louvard, W A Walker

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.8field-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

55 citing papers in PubMed, 130 citations in OpenAlex.

  1. Gastrointestinal tract, its pathophysiology andWorld journal of gastroenterology · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Preterm neonatal immunology at the intestinal interface.Cellular and molecular life sciences : CMLS · 2020
    Review
  9. Bioengineering NovelFrontiers in bioengineering and biotechnology · 2020
    Article
  10. Article
  11. The developmentally regulated fetal enterocyte gene,American journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 3D culture models of tissues under tension.Journal of cell science · 2017
    Review
  17. Article
  18. Review
  19. Frontiers in pediatrics · 2017
    Article
  20. 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

9 authors at 3 institutions in 1 country.

I R SandersonDevelopmental Gastroenterology Laboratory, Harvard Clinical Nutrition Research Center, Massachusetts General Hospital, Boston 02129-2060, USA.
R M Ezzell
M Kedinger
M Erlanger
Z X Xu
E Pringault
S Leon-Robine
D Louvard
W A Walker
Inserm · FRInstitut Curie · FRInstitut Pasteur · FR

Funding

Xenograft and Isograft CoreP01DK033506 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 1986 to 2015
$24.2M
EFFECT OF COLOSTRUM ON GUT MATURATION AND HOST DEFENSER01HD012437 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 1989 to 2013
$2.0M
DEVELOPMENTAL BIOLOGY OF THE ENTEROCYTEF06TW001865 · FIC · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 1992 to 1995
–
FIC NIH HHS F06-TWO 1865NICHD NIH HHS R01-HD12437NIDDK NIH HHS P-30 DK33506
6 · The paper itself

Abstract

The differentiation of small intestinal epithelial cells may require stimulation by microenvironmental factors in vivo. In this study, the effects of mesenchymal and luminal elements in nonmalignant epithelia] cells isolated from the human fetus were studied in vitro. Enterocytes from the human fetus were cultured and microenvironmental factors were added in stages, each stage more closely approximating the microenvironment in vivo. Four stages were examined: epithelial cells derived on plastic from intestinal culture and grown as a cell clone, the same cells grown on connective tissue support, primary epithelial explants grown on fibroblasts with a laminin base, and primary epithelial explants grown on fibroblasts and laminin with n-butyrate added to the incubation medium. The epithelial cell clone dedifferentiated when grown on plastic; however, the cells expressed cytokeratins and villin as evidence of their epithelial cell origin. Human connective tissue matrix from Engelbreth-Holm-Swarm sarcoma cells (Matrigel) modulated their phenotype: alkaline phosphatase activity increased, microvilli developed on their apical surface, and the profile of insulin-like growth factor binding proteins resembled that secreted by differentiated enterocytes. Epithelial cells taken directly from the human fetus as primary cultures and grown as explants on fibroblasts and laminin expressed greater specific enzyme activities in brush border membrane fractions than the cell clone. These activities were enhanced by the luminal molecule sodium butyrate. Thus the sequential addition of connective tissue and luminal molecules to nonmalignant epithelia] cells in vitro induces a spectrum of changes in the epithelial cell phenotype toward full differentiation.

Indexed as

Alkaline PhosphataseBasement MembraneBiomarkersCell DifferentiationCell DivisionCells, CulturedCell SurvivalCollagenDrug CombinationsElectrophysiologyExtracellular MatrixFetusGestational AgeHumansImmunohistochemistryIntestinal MucosaAlkaline PhosphataseBiomarkersCollagenDrug CombinationsKeratinsLamininmatrigelPlasticsProteoglycansSucrase

Identifiers

PMID8755542
PMCPMC38813
OpenAlexW2108342223

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.