EC-SOD induces apoptosis through COX-2 and galectin-7 in the epidermis

J Dermatol Sci. 2012 Feb;65(2):126-33. doi: 10.1016/j.jdermsci.2011.12.013. Epub 2011 Dec 28.

Abstract

Background: Extracellular superoxide dismutase (EC-SOD) is an anti-oxidant enzyme found in the extracellular matrix of tissues, and plays an important role in the prevention of many diseases caused by oxidative stress. However, other functions of EC-SOD in epidermis are not well known.

Objective: We investigated the functions of EC-SOD in epidermis using keratinocyte cell line and EC-SOD transgenic mice.

Methods: Expression of galectin-7 in pEC-SOD transfected cells or skin of EC-SOD transgenic mice was detected by western blot analysis. The percentage of apoptotic cells was determined by propidium iodide staining and subsequent FACS analysis. COX-2 siRNA or scrambled siRNA was transfected into HaCaT cells and western blot analysis was performed to detect pro-apoptotic protein levels.

Results: The epidermis of EC-SOD transgenic mice was thinner than wild type mice. In addition, we showed that the thin epidermis of EC-SOD transgenic mice results from the apoptosis of epidermal cells. To elucidate which molecules are involved in EC-SOD-induced apoptosis, we utilized two-dimensional electrophoresis; the results showed that the epidermis of EC-SOD transgenic mice produces more galectin-7, a pro-apoptotic factor, than the wild type. Furthermore, we showed that the transfection of EC-SOD-expressing plasmids induces the production of galectin-7, and pro-apoptotic proteins in keratinocytes. This suggests that EC-SOD induces apoptosis through increased galectin-7 expression. Finally, we demonstrated that EC-SOD-induced galectin-7 results from the production of COX-2.

Conclusion: Our results imply that EC-SOD plays a role not only as a reactive oxygen species scavenger, but also as a pro-apoptotic factor via COX-2/galectin-7 pathways in the epidermis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Blotting, Western
  • Cell Line
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase 2 Inhibitors / pharmacology
  • Electrophoresis, Gel, Two-Dimensional
  • Epidermis / drug effects
  • Epidermis / enzymology*
  • Epidermis / pathology
  • Flow Cytometry
  • Galectins / genetics
  • Galectins / metabolism*
  • Humans
  • Keratinocytes / drug effects
  • Keratinocytes / enzymology*
  • Keratinocytes / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • RNA Interference
  • Signal Transduction
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism*
  • Transfection

Substances

  • Cyclooxygenase 2 Inhibitors
  • Galectins
  • LGALS7 protein, human
  • Lgals7 protein, mouse
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Superoxide Dismutase