MicroRNA-192 in diabetic kidney glomeruli and its function in TGF-beta-induced collagen expression via inhibition of E-box repressors

Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3432-7. doi: 10.1073/pnas.0611192104. Epub 2007 Feb 20.

Abstract

Key features of diabetic nephropathy (DN) include the accumulation of extracellular matrix proteins such as collagen 1-alpha 1 and -2 (Col1a1 and -2). Transforming growth factor beta1 (TGF-beta), a key regulator of these extracellular matrix genes, is increased in mesangial cells (MC) in DN. By microarray profiling, we noted that TGF-beta increased Col1a2 mRNA in mouse MC (MMC) but also decreased mRNA levels of an E-box repressor, deltaEF1. TGF-beta treatment or short hairpin RNAs targeting deltaEF1 increased enhancer activity of upstream E-box elements in the Col1a2 gene. TGF-beta also decreased the expression of Smad-interacting protein 1 (SIP1), another E-box repressor similar to deltaEF1. Interestingly, we noted that SIP1 is a target of microRNA-192 (miR-192), a key miR highly expressed in the kidney. miR-192 levels also were increased by TGF-beta in MMC. TGF-beta treatment or transfection with miR-192 decreased endogenous SIP1 expression as well as reporter activity of a SIP1 3' UTR-containing luciferase construct in MMC. Conversely, a miR-192 inhibitor enhanced the luciferase activity, confirming SIP1 to be a miR-192 target. Furthermore, miR-192 synergized with deltaEF1 short hairpin RNAs to increase Col1a2 E-box-luc activity. Importantly, the in vivo relevance was noted by the observation that miR-192 levels were enhanced significantly in glomeruli isolated from streptozotocin-injected diabetic mice as well as diabetic db/db mice relative to corresponding nondiabetic controls, in parallel with increased TGF-beta and Col1a2 levels. These results uncover a role for miRs in the kidney and DN in controlling TGF-beta-induced Col1a2 expression by down-regulating E-box repressors.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Line
  • Chromatin Immunoprecipitation
  • Collagen / metabolism*
  • Collagen Type I
  • DNA Primers
  • Diabetic Nephropathies / genetics*
  • Diabetic Nephropathies / metabolism
  • E-Box Elements / genetics
  • Gene Expression Regulation*
  • Homeodomain Proteins / metabolism
  • Mesangial Cells / metabolism*
  • Mice
  • MicroRNAs / metabolism*
  • Nerve Tissue Proteins / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Repressor Proteins / antagonists & inhibitors*
  • Repressor Proteins / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors / metabolism
  • Transforming Growth Factor beta / metabolism*

Substances

  • Collagen Type I
  • DNA Primers
  • Homeodomain Proteins
  • MicroRNAs
  • Nerve Tissue Proteins
  • Repressor Proteins
  • Sip1 protein, mouse
  • Transcription Factors
  • Transforming Growth Factor beta
  • Zfhx1a protein, mouse
  • Collagen