Evidence map›Paper›PMID 42494780›Full record

ArticleJournal of extracellular biology2026

Secretion of Extracellular Vesicles Into the Mesenteric Lymph During Fasting and Lipid Absorption.

Tianyu Hang, Rita Wang, Kundanika Mukherjee, Uday Sandhu, Fengxia Xiao, Dylan Burger, Changting Xiao

Abstract read
In one paragraph

Article in Journal of extracellular biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Tianyu HangDepartment of Anatomy, Physiology and Pharmacology, College of Medicine University of Saskatchewan Saskatoon Saskatchewan Canada.ORCID https://orcid.org/0000-0003-3670-837X
Rita WangDepartment of Anatomy, Physiology and Pharmacology, College of Medicine University of Saskatchewan Saskatoon Saskatchewan Canada.
Kundanika MukherjeeDepartment of Anatomy, Physiology and Pharmacology, College of Medicine University of Saskatchewan Saskatoon Saskatchewan Canada.
Uday SandhuDepartment of Anatomy, Physiology and Pharmacology, College of Medicine University of Saskatchewan Saskatoon Saskatchewan Canada.
Fengxia XiaoKidney Research Centre Ottawa Hospital Research Institute Ottawa Ontario Canada.
Dylan BurgerKidney Research Centre Ottawa Hospital Research Institute Ottawa Ontario Canada.ORCID https://orcid.org/0000-0003-3951-2911
Changting XiaoDepartment of Anatomy, Physiology and Pharmacology, College of Medicine University of Saskatchewan Saskatoon Saskatchewan Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intestine plays critical roles in nutrient homeostasis and systemic health. The small intestine is the major organ that packages dietary lipids into chylomicrons and secretes them into the mesenteric lymph. Extracellular vesicles (EVs) as a mechanism for cell-to-cell communication often exhibit organ specific characteristics. EV secretion from the intestine into the mesenteric lymph-a unique biofluid-remains unexplored. To characterize gut-derived EVs, Sprague-Dawley rats were surgically implanted with cannula in the mesenteric lymph duct (for lymph collection) and the duodenum (for lipid infusion). Lymph fluid was collected for assessment of EV secretion. EVs in lymph fluids collected before and after lipid infusion were characterized by transmission electron microscopy, nanoparticle tracking analysis, and further analyzed by flow cytometry with antibodies against CD63, CD81, CD9 and apolipoprotein B (ApoB). Lipid infusion increased lymph triglyceride output peaking at 2 h. Lymph fluids contained EVs with diameters in the range of 20 to 300 nm and the signals of specific EV markers CD63, CD81 and CD9 were significantly elevated following lipid infusion. Depletion of chylomicrons from lymph had differential effects on the percentage and intensity of CD63, CD81 and CD9. In addition, these EVs exhibited distinct patterns in ApoB

Identifiers

PMID42494780
PMCPMC13393292

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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.