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Updated: Jan 27, 2026

The Mesenteric Lymph Duct Cannulated Rat Model: Application to the Assessment of Intestinal Lymphatic Drug Transport
Published on: March 6, 2015
Extracellular RNA Profile in Mesenteric Lymph from Exemplar Rat Models of Acute and Critical Illness
Jiwon Hong1,2, Cherie Blenkiron1,3, Peter Tsai3
1School of Biological Sciences, Faculty of Science, University of Auckland, Auckland, New Zealand.
Abstract:
Mesenteric lymph (ML) has been implicated in the development of multiple organ dysfunction syndrome in critical illness. Extracellular RNAs play a role in cell-to-cell communication during physiological and disease processes but they are rarely studied in ML. We aimed at examining the RNA profiles of peripheral plasma, ML, and ML's extracellular vesicle (ML-EV) and triglyceride-rich lipoprotein (ML-TRL) fractions, obtained from rodent models of critical illness. We collected ML for 5 hours from rodent models of critical illness [Acute Pancreatitis, Cecal Ligation and Incision (CLI), Gut Ischemia-Reperfusion (IR)] and matching Sham control rats. ML-EV and ML-TRL fractions were also isolated. RNA sequencing was performed on the RNA extracted from ML, ML-EV, ML-TRL, and plasma by using the Ion Torrent Personal Genome Machine platform. RNA sequences were searched using the Basic Local Alignment Search Tool against rat genome and RefSeq, microRNA (miRNA), genomic tRNA, functional RNA, and Genbank nucleotide databases, and the read counts were analyzed. Each sample type had a distinct RNA profile. ML contained more RNA per volume and a larger proportion of tRNA fragments than plasma. ML-EVs were enriched with miRNA, whereas ML-TRLs contained low absolute amounts of RNA. The RNA size profiles for CLI and Gut IR were different from Sham. ML carried intestinal RNAs and in a CLI model it was significantly enriched with bacterial RNA sequences. We found the distinct but diverse RNA profiles of ML and its compartments, and their different profiles in critical illness. Intestinal-derived small RNAs in ML may have a direct role in critical illness and utility as potential biomarkers.
Insights
Mesenteric lymph (ML) contains distinct RNA profiles, varying with critical illness conditions. Intestinal RNAs in ML may serve as biomarkers for critical illness, offering new diagnostic possibilities.
Area of Science:
- Biochemistry
- Molecular Biology
- Critical Care Medicine
Background:
- Mesenteric lymph (ML) is linked to multiple organ dysfunction syndrome in critical illness.
- Extracellular RNAs mediate cell-to-cell communication but are understudied in ML.
Purpose of the Study:
- To characterize RNA profiles in peripheral plasma, ML, ML-derived extracellular vesicles (ML-EVs), and ML-derived triglyceride-rich lipoproteins (ML-TRLs) in rodent models of critical illness.
- To investigate the impact of critical illness conditions on these RNA profiles.
Main Methods:
- Collected ML and plasma from rodent models of acute pancreatitis, cecal ligation and incision (CLI), and gut ischemia-reperfusion (IR), alongside sham controls.
- Isolated ML-EV and ML-TRL fractions.
- Performed RNA sequencing on extracted RNA using Ion Torrent technology and analyzed sequences against various genomic and nucleotide databases.
Main Results:
- Distinct RNA profiles were observed across different sample types (ML, plasma, ML-EVs, ML-TRLs).
- ML showed higher RNA concentration and a greater proportion of tRNA fragments compared to plasma.
- ML-EVs were enriched in microRNAs (miRNAs), while ML-TRLs had low RNA amounts.
- RNA profiles differed between critical illness models (CLI, IR) and sham controls.
- ML contained intestinal RNAs, with significant enrichment of bacterial RNA sequences in the CLI model.
Conclusions:
- Mesenteric lymph and its sub-compartments exhibit unique and diverse RNA profiles.
- These RNA profiles change significantly during critical illness.
- Intestinal-derived small RNAs within ML are potential contributors to critical illness pathogenesis and may serve as valuable biomarkers.
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