Evidence map›Paper›PMID 28159868›Full record

ArticleJournal of lipid research2017

Using primary murine intestinal enteroids to study dietary TAG absorption, lipoprotein synthesis, and the role of apoC-III in the intestine.

Javeed Jattan, Cayla Rodia, Diana Li, Adama Diakhate, Hongli Dong, Amy Bataille, Noah F Shroyer, Alison B Kohan

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
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  4. The Use of Organoid Cultures in Advancing Nutrition Research.Advances in nutrition (Bethesda, Md.) · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. From worms to humans: Understanding intestinal lipid metabolism via model organisms.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2023
    Review
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  10. Article
  11. Article
  12. Review
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  14. Article
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  17. Article
  18. Article
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  20. Key differences between apoC-III regulation and expression in intestine and liver.Biochemical and biophysical research communications · 2017
    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.

Javeed JattanDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT.
Cayla RodiaDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT.
Diana LiDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT.
Adama DiakhateDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT.
Hongli DongDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT.
Amy BatailleDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT.
Noah F ShroyerDepartment of Medicine Section of Gastroenterology and Hepatology, Baylor College of Medicine, Houston, TX.
Alison B KohanDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT alison.kohan@uconn.edu.
University of Connecticut · USBaylor College of Medicine · US

Funding

Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Hashem B El-Serag · 2001 to 2026
$28.3M
A unique role for apoC-III in intestinal lipoprotein synthesis and secretionK01DK101663 · NIDDK · UNIVERSITY OF CONNECTICUT STORRS · PI KOHAN, ALISON BLOOM · 2014 to 2018
$779k
Determining the Mechanism for ApoC-III Stimulation of IL-10 and Tregs in the Intestine: Is this Novel Effect Beneficial?R03DK116011 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KOHAN, ALISON BLOOM · 2019 to 2020
$238k
NIDDK NIH HHS K01 DK101663NIDDK NIH HHS P30 DK056338NIDDK NIH HHS R03 DK116011
6 · The paper itself

Abstract

Since its initial report in 2009, the intestinal enteroid culture system has been a powerful tool used to study stem cell biology and development in the gastrointestinal tract. However, a major question is whether enteroids retain intestinal function and physiology. There have been significant contributions describing ion transport physiology of human intestinal organoid cultures, as well as physiology of gastric organoids, but critical studies on dietary fat absorption and chylomicron synthesis in primary intestinal enteroids have not been undertaken. Here we report that primary murine enteroid cultures recapitulate in vivo intestinal lipoprotein synthesis and secretion, and reflect key aspects of the physiology of intact intestine in regard to dietary fat absorption. We also show that enteroids can be used to elucidate intestinal mechanisms behind CVD risk factors, including tissue-specific apolipoprotein functions. Using enteroids, we show that intestinal apoC-III overexpression results in the secretion of smaller, less dense chylomicron particles along with reduced triacylglycerol secretion from the intestine. This model significantly expands our ability to test how specific genes or genetic polymorphisms function in dietary fat absorption and the precise intestinal mechanisms that are critical in the etiology of metabolic disease.

Indexed as

Absorption, PhysicochemicalAnimalsApolipoprotein C-IIICell DifferentiationChylomicronsDietary FatsHumansIntestinal MucosaIntestinesMiceMice, Inbred C57BLMice, TransgenicOrgan SpecificityTriglyceridesApolipoprotein C-IIIChylomicronsDietary FatsTriglyceridesapolipoprotein C-IIIchylomicronsdietary fat absorptionintestinal lipid transportorganoidsstem cellstriglyceride

Identifiers

PMID28159868
PMCPMC5408603
OpenAlexW2584489823

What Socratic 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 Socratic graph.