Targeted deletion of Dicer from proximal tubules protects against renal ischemia-reperfusion injury

J Am Soc Nephrol. 2010 May;21(5):756-61. doi: 10.1681/ASN.2009070718. Epub 2010 Apr 1.


MicroRNAs are endogenous, noncoding, small RNAs that regulate expression and function of genes, but little is known about regulation of microRNA in the kidneys under normal or pathologic states. Here, we generated a mouse model in which the proximal tubular cells lack Dicer, a key enzyme for microRNA production. These mice had normal renal function and histology under control conditions despite a global downregulation of microRNAs in the renal cortex; however, these animals were remarkably resistant to renal ischemia-reperfusion injury (IRI), showing significantly better renal function, less tissue damage, lower tubular apoptosis, and improved survival compared with their wild-type littermates. Microarray analysis showed altered expression of specific microRNAs during renal IRI. Taken together, these results demonstrate evidence for a pathogenic role of Dicer and associated microRNAs in renal IRI.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acute Kidney Injury / etiology
  • Acute Kidney Injury / metabolism*
  • Animals
  • DEAD-box RNA Helicases / metabolism*
  • Endoribonucleases / metabolism*
  • Gene Knockout Techniques
  • Kidney Tubules, Proximal / metabolism*
  • Male
  • Mice
  • Mice, Knockout
  • MicroRNAs / metabolism*
  • Oligonucleotide Array Sequence Analysis
  • Reperfusion Injury / complications
  • Reperfusion Injury / metabolism*
  • Ribonuclease III


  • MicroRNAs
  • Endoribonucleases
  • Dicer1 protein, mouse
  • Ribonuclease III
  • DEAD-box RNA Helicases