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Detection of microRNA Expression in Peritoneal Membrane of Rats Using Quantitative Real-time PCR
Published on: June 27, 2017
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Expression profiles and circulation dynamics of rat mesenteric lymph microRNAs
Wakako Sakamoto1, Tomohiko Masuno2, Hiroyuki Yokota2
1Department of Molecular Medicine and Anatomy, Nippon Medical School, Tokyo 113‑8602, Japan.
Molecular Medicine Reports
|March 6, 2017
Summary
Mesenteric lymph contains numerous microRNAs (miRNAs), some of which are exosome-bound. These lymph miRNAs are delivered via mesenteric lymphatics, with lungs clearing exosomal miRNAs.
Area of Science:
- Immunology
- Molecular Biology
- Physiology
Background:
- Mesenteric lymph is crucial for immune cell transport and homeostasis.
- Limited research exists on mesenteric lymph microRNA (miRNA) profiles and circulation.
- Understanding lymph miRNA dynamics is vital for immune and metabolic research.
Purpose of the Study:
- To comprehensively analyze miRNAs in normal rodent mesenteric lymph.
- To investigate the presence and circulation of lymph miRNAs, particularly in exosomes.
- To determine the in vivo fate and organ distribution of mesenteric lymph miRNAs.
Main Methods:
- Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) array analysis of 375 miRNAs in rat mesenteric lymph.
- Differential centrifugation to assess exosomal presence of miR-150.
- In vivo tracing of cel-miR-238-3p-labeled exosomes derived from rat small intestine epithelial cells (IEC-6).
Main Results:
- Detected 287 miRNAs in mesenteric lymph, with 21 significantly different from plasma.
- Identified cell-free miR-150 within the exosome-containing microsomal fraction.
- In vivo studies showed exosomal cel-miR-238-3p predominantly accumulating in the lungs, indicating lung as the primary clearance organ.
Conclusions:
- Mesenteric lymph harbors a distinct miRNA profile compared to plasma.
- miRNAs are present in exosomes within mesenteric lymph.
- Exosomal miRNAs from mesenteric lymph are cleared primarily by the lungs, suggesting a role in lung gene expression modulation.

