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.

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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