Evidence map›Paper›PMID 24798584›Full record

ArticleMolecular pharmaceutics2014

3-D intestinal scaffolds for evaluating the therapeutic potential of probiotics.

Cait M Costello, Rachel M Sorna, Yih-Lin Goh, Ivana Cengic, Nina K Jain, John C March

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. The Game for Three:Frontiers in microbiology · 2022
    Review
  11. The Progress of Intestinal Epithelial Models from Cell Lines to Gut-On-Chip.International journal of molecular sciences · 2021
    Review
  12. Review
  13. ACS synthetic biology · 2021
    Article
  14. Article
  15. Gut bioengineering strategies for regenerative medicine.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Review
  16. Cell-Free Supernatant ofFrontiers in microbiology · 2021
    Article
  17. Review
  18. Review
  19. Article
  20. Biosensing in Smart Engineered Probiotics.Biotechnology journal · 2020
    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

6 authors at 1 institution in 1 country.

Cait M CostelloDepartment of Biological and Environmental Engineering, Cornell University , Ithaca, New York 14853, United States.
Rachel M Sorna
Yih-Lin Goh
Ivana Cengic
Nina K Jain
John C March
Cornell University · US

Funding

Engineering commensal bacteria as therapeutic signal mediatorsDP2OD007155 · OD · CORNELL UNIVERSITY · PI MARCH, JOHN C · 2010 to 2015
$2.9M
NIH HHS 1DP2OD007155-01NIH HHS DP2 OD007155
6 · The paper itself

Abstract

Biomimetic in vitro intestinal models are becoming useful tools for studying host-microbial interactions. In the past, these models have typically been limited to simple cultures on 2-D scaffolds or Transwell inserts, but it is widely understood that epithelial cells cultured in 3-D environments exhibit different phenotypes that are more reflective of native tissue, and that different microbial species will preferentially adhere to select locations along the intestinal villi. We used a synthetic 3-D tissue scaffold with villous features that could support the coculture of epithelial cell types with select bacterial populations. Our end goal was to establish microbial niches along the crypt-villus axis in order to mimic the natural microenvironment of the small intestine, which could potentially provide new insights into microbe-induced intestinal disorders, as well as enabling targeted probiotic therapies. We recreated the surface topography of the small intestine by fabricating a biodegradable and biocompatible villous scaffold using poly lactic-glycolic acid to enable the culture of Caco-2 with differentiation along the crypt-villus axis in a similar manner to native intestines. This was then used as a platform to mimic the adhesion and invasion profiles of both Salmonella and Pseudomonas, and assess the therapeutic potential of Lactobacillus and commensal Escherichia coli in a 3-D setting. We found that, in a 3-D environment, Lactobacillus is more successful at displacing pathogens, whereas Nissle is more effective at inhibiting pathogen adhesion.

Indexed as

BacteriaBacterial AdhesionBiomimeticsCaco-2 CellsCell DifferentiationDrug EvaluationEpithelial CellsHumansIntestine, SmallProbioticsTissue Scaffolds

Identifiers

PMID24798584
PMCPMC4096232
OpenAlexW2325219935

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.