Glycyrrhizin protects γ-irradiated mice from gut bacteria-associated infectious complications by improving miR-222-associated Gas5 RNA reduction in macrophages of the bacterial translocation site

Ichiaki Ito, Bradford D. Loucas, Sumihiro Suzuki, Makiko Kobayashi, Fujio Suzuki

Research output: Contribution to journalArticlepeer-review

Abstract

Gut bacteria-associated sepsis is a serious concern in patients with gastrointestinal acute radiation syndrome (GIARS). In our previous studies, gut bacteria-associated sepsis caused high mortality rates in mice exposed to 6-9 Gy of γ-rays. IL-12+CD38+ iNOS+ Mφ (M1Mφ) located in the bacterial translocation site (mesenteric lymph nodes [MLNs]) of unirradiated mice were characterized as host defense antibacterial effector cells. However, cells isolated from the MLNs of GIARS mice were mostly CCL1+IL-10+LIGHT+miR-27a+ Mφ (M2bMφ, inhibitor cells for the M1Mφ polarization). Reduced long noncoding RNA Gas5 and increased miR-222 expression in MLN-Mφ influenced by the irradiation were shown to be associated with M2bMφ polarization. In this study, the mortality of mice exposed to 7 Gy of γ-rays (7 Gy GIARS mice) was completely controlled after the administration of glycyrrhizin (GL), a major active ingredient in licorice root (Glycyrrhiza glabra). Bacterial translocation and subsequent sepsis were minimal in 7 Gy GIARS mice treated with GL. Increased Gas5 RNA level and decreased miR-222 expression were shown in MLN-Mφ isolated from 7 Gy GIARS mice treated with GL, and these macrophages did not display any properties of M2bMφ. These results indicate that gut bacteria-associated sepsis in 7 Gy GIARS mice was controlled by the GL through the inhibition of M2bMφ polarization at the bacteria translocation site. Expression of Ccl1, a gene required for M2bMφ survival, is silenced in the MLNs of 7 Gy GIARS mice because of Gas5 RNA, which is increased in these cells after the suppression of miR-222 (a Gas5 RNA expression inhibitor) by the GL.

Original languageEnglish (US)
Pages (from-to)1255-1262
Number of pages8
JournalJournal of Immunology
Volume204
Issue number5
DOIs
StatePublished - Mar 1 2020

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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