Evidence map›Paper›PMID 28265783›Full record

ArticleHistochemistry and cell biology2017

T84 monolayers are superior to Caco-2 as a model system of colonocytes.

Sarah Devriese, Lien Van den Bossche, Sophie Van Welden, Tom Holvoet, Iris Pinheiro, Pieter Hindryckx, Martine De Vos, Debby Laukens

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Histochemistry and cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
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  7. Bioscience of microbiota, food and health · 2026
    Article
  8. Review
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  11. Emerging advances in intestinal models for in vitro preclinical research.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
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  19. In Vitro Models for Investigating Intestinal Host-Pathogen Interactions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  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

8 authors at 2 institutions in 1 country.

Sarah DevrieseDepartment of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium.
Lien Van den BosscheDepartment of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium.
Sophie Van WeldenDepartment of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium.
Tom HolvoetDepartment of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium.
Iris PinheiroProDigest BVBA, Technologiepark 3, 9052, Ghent, Belgium.
Pieter HindryckxDepartment of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium.
Martine De VosDepartment of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium.
Debby LaukensDepartment of Gastroenterology, Ghent University, De Pintelaan 185, 0MRB2, 9000, Ghent, Belgium. debby.laukens@ugent.be.
Ghent University Hospital · BEProDigest (Belgium) · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colonic adenocarcinoma-derived Caco-2 and T84 epithelial cell lines are frequently used as in vitro model systems of functional epithelial barriers. Both are utilised interchangeably despite evidence that differentiated Caco-2 cells are more reminiscent of small intestinal enterocytes than of colonocytes, whereas differentiated T84 cells are less well characterised. The aim of this study was, therefore, to further characterise and compare differentiated Caco-2 and T84 cells. The objectives were to (1) compare the brush border morphology, (2) measure the expression of enterocyte- and colonocyte-specific genes and (3) compare their response to butyrate, which is dependent on the monocarboxylate transporter 1 (MCT1), an apical protein expressed primarily in colonocytes. T84 microvilli were significantly shorter than those of Caco-2 cells, which is a characteristic difference between small intestinal enterocytes and colonocytes. Also, enterocyte-associated brush border enzymes expressed in differentiated Caco-2 cells were not increased during T84 maturation, whereas colonic markers such as MCT1 were more abundant in differentiated T84 cells compared to differentiated Caco-2 cells. Consequently, T84 cells displayed a dose-responsive improvement of barrier function towards butyrate, which was absent in Caco-2 cells. On the other hand, differences in epithelial toll-like receptor expression between Caco-2 and T84 monolayers did not result in a corresponding differential functional response. We conclude that differentiated Caco-2 and T84 cells have distinct morphological, biochemical and functional characteristics, suggesting that T84 cells do not acquire the biochemical signature of mature small intestinal enterocytes like Caco-2 cells, but retain much of their original colonic characteristics throughout differentiation. These findings can help investigators select the appropriate intestinal epithelial cell line for specific in vitro research purposes.

Indexed as

Models, BiologicalAnimalsCaco-2 CellsColonHumansTumor Cells, CulturedColonocyteDifferentiationEnterocyteEpithelial cellsMCT1

Identifiers

PMID28265783
OpenAlexW2594724854

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.