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Rivkin, M.* ; Simerzin, A.* ; Zorde-Khvalevsky, E.* ; Chai, C.* ; Yuval, J.B.* ; Rosenberg, N.* ; Harari-Steinfeld, R.* ; Schneider, R.* ; Amir, G.* ; Condiotti, R.* ; Heikenwälder, M. ; Weber, A.* ; Schramm, C.* ; Wege, H.* ; Kluwe, J.* ; Galun, E.* ; Giladi, H.*

Inflammation-induced expression and secretion of microRNA 122 leads to reduced blood levels of kidney-derived erythropoietin and anemia.

Gastroenterology 151, 999-1010.e3 (2016)
Postprint DOI PMC
Open Access Green
BACKGROUND & AIM: Anemia is commonly associated with acute and chronic inflammation, but the mechanisms of their interaction are not clear. We investigated whether microRNA 122 (MIR122), which is generated in the liver and is secreted into the blood, is involved in the development of anemia associated with inflammation. METHODS: We characterized the primary transcript of the human liver-specific MIR122 using northern blot, quantitative real-time PCR, and 3' and 5' RACE analyses. We studied regulation of MIR122 in human hepatocellular carcinoma (HCC) cell lines (Huh7 and HepG2) as well as in C57BL/6 and mice with disruption of the tumor necrosis factor gene (Tnf). Liver tissues were collected and analyzed by bioluminescence imaging or immunofluorescence. Inflammation in mice was induced by lipopolysaccharide (LPS) or by cerulein injections. Mice were given 4 successive injections of LPS, leading to inflammation-induced anemia. Steatohepatitis was induced with a choline-deficient high-fat diet. Hemolytic anemia was stimulated by phenylhydrazine injection. MIR122 was inhibited in mice by tail-vein injection of antogomiR-122 (an oligonucleotide antagonist of MIR122). MicroRNA and mRNA levels were determined by quantitative real time PCR. RESULTS: The primary transcript of MIR122 spanned 5 kb, comprising 3 exons; the third encodes MIR122. Within the MIR122 promoter region we identified a nuclear factor-κB (NF-κB) binding site and demonstrated that RELA, as well as activators of NF-κB (TNF and LPS), increased promoter activity of MIR122. Administration of LPS to mice induced secretion of MIR122 into blood, which required TNF. Secreted MIR122 reached the kidney and reduced expression of erythropoietin (Epo), which we identified as a MIR122 target gene. Injection of mice with antagomiR-122 increased blood levels of EPO, reticulocytes, and hemoglobin. We found an inverse relationship between blood levels of MIR122 and EPO in mice with acute pancreatitis or steatohepatitis, and also in patients with acute inflammation. CONCLUSION: In mice, we found that LPS-induced inflammation increases blood levels of MIR122, which reduces expression of Epo in the kidney; this is a mechanism of inflammation-induced anemia. Strategies to block MIR122 in patients with inflammation could reduce the development or progression of anemia.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Nash ; Microbiome ; Mouse Model ; Red Blood Cells; Nf-kappa-b; Human Hepatocellular-carcinoma; Gene-expression; Circulating Micrornas; Mir-122 Expression; Liver-cancer; Activation; Therapy; Cells; Pancreatitis
ISSN (print) / ISBN 0016-5085
e-ISSN 1528-0012
Journal Gastroenterology
Quellenangaben Volume: 151, Issue: 5, Pages: 999-1010.e3 Article Number: , Supplement: ,
Publisher Elsevier
Publishing Place Philadelphia
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Virology (VIRO)