TNF-α promotes human retinal pigment epithelial (RPE) cell migration by inducing matrix metallopeptidase 9 (MMP-9) expression through activation of Akt/mTORC1 signaling

Biochem Biophys Res Commun. 2012 Aug 17;425(1):33-8. doi: 10.1016/j.bbrc.2012.07.044. Epub 2012 Jul 20.

Abstract

Tumor necrosis factor-alpha (TNF-α) promotes in vitro retinal pigment epithelial (RPE) cell migration to initiate proliferative vitreoretinopathy (PVR). Here we report that TNF-α promotes human RPE cell migration by inducing matrix metallopeptidase 9 (MMP-9) expression. Inhibition of MMP-9 by its inhibitor or its neutralizing antibody inhibited TNF-α-induced in vitro RPE cell migration. Reversely, exogenously-added active MMP-9 promoted RPE cell migration. Suppression Akt/mTOR complex 1(mTORC1) activation by LY 294002 and rapamycin inhibited TNF-α-mediated MMP-9 expression. To introduce a constitutively active Akt (CA-Akt) in cultured RPE cells increased MMP-9 expression, and to block mTORC1 activation by rapamycin inhibited its effect. RNA interference (RNAi)-mediated silencing of SIN1, a key component of mTOR complex 2 (mTORC2), had no effect on MMP-9 expression or secretion. In conclusion, this study suggest that TNF-α promotes RPE cell migration by inducing MMP-9 expression through activation of Akt/ mTORC1, but not mTORC2 signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Cell Movement / drug effects*
  • Cell Movement / physiology
  • Cells, Cultured
  • Humans
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Mechanistic Target of Rapamycin Complex 1
  • Multiprotein Complexes
  • Pigment Epithelium of Eye / drug effects*
  • Pigment Epithelium of Eye / enzymology
  • Pigment Epithelium of Eye / physiology
  • Proteins / metabolism*
  • Proto-Oncogene Proteins c-akt / biosynthesis*
  • RNA Interference
  • Signal Transduction
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Vitreoretinopathy, Proliferative / enzymology
  • Vitreoretinopathy, Proliferative / pathology

Substances

  • Adaptor Proteins, Signal Transducing
  • MAPKAP1 protein, human
  • Multiprotein Complexes
  • Proteins
  • Tumor Necrosis Factor-alpha
  • Mechanistic Target of Rapamycin Complex 1
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Matrix Metalloproteinase 9