Evidence map›Paper›PMID 19396808›Full record

ArticleBiotechnology and bioengineering2009

A tissue-engineered model of the intestinal lacteal for evaluating lipid transport by lymphatics.

J Brandon Dixon, Sandeep Raghunathan, Melody A Swartz

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

47 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. GPR182 is a lipoprotein receptor for dietary fat absorption.The Journal of clinical investigation · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Understanding the Lymphatic System: Tissue-on-Chip Modeling.Annual review of biomedical engineering · 2025
    Review
  8. Intravital imaging of translocated bacteria via fluorogenic labeling of gut microbiota in situ.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Matrix stiffness primes lymphatic tube formation directed by vascular endothelial growth factor-C.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  15. Review
  16. Specialized Pro-Resolving Mediators and the Lymphatic System.International journal of molecular sciences · 2021
    Review
  17. Gut bioengineering strategies for regenerative medicine.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Review
  18. Article
  19. 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

3 authors at 1 institution in 2 countries.

J Brandon DixonInstitute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland.
Sandeep Raghunathan
Melody A Swartz
École Polytechnique Fédérale de Lausanne · CH

Funding

Lymph vs. blood angiogenesis: functional differences in*R01HL075217 · NHLBI · NORTHWESTERN UNIVERSITY · PI SWARTZ, MELODY A · 2003 to 2006
$1.2M
Quantifying the role of lymphatics in lipid metabolism and transportR00HL091133 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI DIXON, JAMES BRANDON · 2009 to 2011
$716k
Quantifying the role of lymphatics in lipid metabolism and transportK99HL091133 · NHLBI · NORTHWESTERN UNIVERSITY · PI DIXON, JAMES BRANDON · 2008 to 2008
$90k
NHLBI NIH HHS HL075217NHLBI NIH HHS K99 HL091133NHLBI NIH HHS R00 HL091133NHLBI NIH HHS R01 HL075217PHS HHS K99 KHL091133A
6 · The paper itself

Abstract

Lacteals are the entry point of all dietary lipids into the circulation, yet little is known about the active regulation of lipid uptake by these lymphatic vessels, and there lacks in vitro models to study the lacteal-enterocyte interface. We describe an in vitro model of the human intestinal microenvironment containing differentiated Caco-2 cells and lymphatic endothelial cells (LECs). We characterize the model for fatty acid, lipoprotein, albumin, and dextran transport, and compare to qualitative uptake of fatty acids into lacteals in vivo. We demonstrate relevant morphological features of both cell types and strongly polarized transport of fatty acid in the intestinal-to-lymphatic direction. We found much higher transport rates of lipid than of dextran or albumin across the lymphatic endothelial monolayer, suggesting most lipid transport is active and intracellular. This was confirmed with confocal imaging of Bodipy, a fluorescent fatty acid, along with transmission electron microscopy. Since our model recapitulates crucial aspects of the in vivo lymphatic-enterocyte interface, it is useful for studying the biology of lipid transport by lymphatics and as a tool for screening drugs and nanoparticles that target intestinal lymphatics.

Indexed as

Lipid MetabolismAlbuminsDextransEndothelial CellsEpithelial CellsHumansIntestinal MucosaLipoproteinsMicroscopy, ConfocalMicroscopy, ElectronTissue EngineeringAlbuminsDextransLipoproteins

Identifiers

PMID19396808
PMCPMC3132564
OpenAlexW2160157834

What OpenQuestion holds

Textmetadata
LicenceTDM
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.