Renal medullary MicroRNAs in dahl salt-sensitive rats: MiR-29b regulates several collagens and related genes

Academic Article

Abstract

  • MicroRNAs are endogenous repressors of gene expression. We examined microRNAs in the renal medulla of Dahl salt-sensitive rats and consomic SS-13 rats. Salt-induced hypertension and renal injury in Dahl salt-sensitive rats, particularly medullary interstitial fibrosis, have been shown previously to be substantially attenuated in SS-13 rats. Of 377 microRNAs examined, 5 were found to be differentially expressed between Dahl salt-sensitive rats and consomic SS-13 rats receiving a high-salt diet. Real-time PCR analysis demonstrated that high-salt diets induced substantial upregulation of miR-29b in the renal medulla of SS-13 rats but not in SS rats. miR-29b was predicted to regulate 20 collagen genes, matrix metalloproteinase 2 (Mmp2), integrin β1 (Itgb1), and other genes related to the extracellular matrix. Expression of 9 collagen genes and Mmp2 was upregulated by a high-salt diet in the renal medulla of SS rats, but not in SS-13 rats, an expression pattern opposite to miR-29b. Knockdown of miR-29b in the kidneys of SS-13 rats resulted in upregulation of several collagen genes. miR-29b reduced expression levels of several collagen genes and Itgb1 in cultured rat renal medullary epithelial cells. Moreover, miR-29b suppressed the activity of luciferase when the reporter gene was linked to a 3′-untranslated segment of collagen genes Col1a1, Col3a1, Col4a1, Col5a1, Col5a2, Col5a3, Col7a1, Col8a1, Mmp2, or Itgb1 but not Col12a1. The result demonstrated broad effects of miR-29b on a large number of collagens and genes related to the extracellular matrix and suggested involvement of miR-29b in the protection from renal medullary injury in SS-13 rats. © 2010 American Heart Association, Inc.
  • Authors

    Published In

  • Hypertension  Journal
  • Digital Object Identifier (doi)

    Pubmed Id

  • 23938028
  • Author List

  • Liu Y; Taylor NE; Lu L; Usa K; Cowley AW; Ferreri NR; Yeo NC; Liang M
  • Start Page

  • 974
  • End Page

  • 982
  • Volume

  • 55
  • Issue

  • 4