Expression, circulation, and excretion profile of microRNA-21, -155, and -18a following acute kidney injury

• Published in: Toxicological sciences Vol. 129; no. 2; pp. 256 - 267
• Main Authors: Saikumar, Janani, Hoffmann, Dana, Kim, Tae-Min, Gonzalez, Victoria Ramirez, Zhang, Qin, Goering, Peter L, Brown, Ronald P, Bijol, Vanesa, Park, Peter J, Waikar, Sushrut S, Vaidya, Vishal S
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01.10.2012
• Subjects: Acute Kidney Injury - chemically induced; Acute Kidney Injury - genetics; Acute Kidney Injury - urine; Algorithms; Animals; Case-Control Studies; Gentamicins - toxicity; Humans; MicroRNAs - blood; MicroRNAs - genetics; MicroRNAs - urine; Polymerase Chain Reaction; Rats; Rats, Wistar
• ISSN: 1096-6080; 1096-0929
• DOI: 10.1093/toxsci/kfs210

MicroRNAs (miRNAs) are endogenous noncoding RNA molecules that are involved in post-transcriptional gene silencing. Using global miRNA expression profiling, we found miR-21, -155, and 18a to be highly upregulated in rat kidneys following tubular injury induced by ischemia/reperfusion (I/R) or gentamicin administration. Mir-21 and -155 also showed decreased expression patterns in blood and urinary supernatants in both models of kidney injury. Furthermore, urinary levels of miR-21 increased 1.2-fold in patients with clinical diagnosis of acute kidney injury (AKI) (n = 22) as compared with healthy volunteers (n = 25) (p < 0.05), and miR-155 decreased 1.5-fold in patients with AKI (p < 0.01). We identified 29 messenger RNA core targets of these 3 miRNAs using the context likelihood of relatedness algorithm and found these predicted gene targets to be highly enriched for genes associated with apoptosis or cell proliferation. Taken together, these results suggest that miRNA-21 and -155 could potentially serve as translational biomarkers for detection of AKI and may play a critical role in the pathogenesis of kidney injury and tissue repair process.