Acceleration of Apoptosis by Extracellular Basic pH in a 3D Human Skin Equivalent System

Pharmacology. 2017;100(1-2):98-104. doi: 10.1159/000475884. Epub 2017 May 12.

Abstract

Previously, we have shown that extracellular basic pH plays a significant role in both the direct and indirect regulation of cellular processes in a wound; this in turn affects the wound-healing process. Several studies have demonstrated the importance of apoptosis modulation in the wound-healing process, especially in removing inflammatory cells and in inhibiting scar formation. However, the effects of extracellular basic pH on wound healing-related skin damage are yet to be examined. Therefore, we investigated the induction of accelerated apoptosis by extracellular basic pH in skin. Apoptosis-related protein levels were measured using an array kit, target protein expression levels were detected by immunostaining, lactate dehydrogenase was analyzed spectrophotometrically, and Annexin V levels were measured by fluorescence staining. Basic pH (8.40) strongly upregulated extrinsic apoptosis proteins (Fas, high temperature requirement A, and p21) and slightly upregulated intrinsic apoptosis proteins (cytochrome c, B-cell lymphoma 2 [Bcl-2], Bcl-2-associated death promoter, and Bcl-2-like protein 4) in a 3D human skin equivalent system. Moreover, basic pH (8.40) induced heat shock protein (HSP) 60 and 70. In addition, basic pH-exposed Fas- and HSP60-knockdown cells showed significantly decreased levels of apoptosis. Taken together, these results indicate that extracellular basic pH increases early-stage apoptosis through Fas/FasL via modulation of HSP60 and HSP70.

Keywords: 3D human skin equivalent system; Apoptosis; Heat shock proteins; pH.

MeSH terms

  • Annexin A5 / analysis
  • Apoptosis / physiology*
  • Chaperonin 60 / metabolism
  • Extracellular Space / metabolism*
  • Fas Ligand Protein / metabolism
  • Gene Knockdown Techniques
  • HSP70 Heat-Shock Proteins / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • L-Lactate Dehydrogenase / metabolism
  • Skin / metabolism*
  • Spectrophotometry
  • Wound Healing / physiology*
  • fas Receptor / metabolism

Substances

  • Annexin A5
  • Chaperonin 60
  • FAS protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • HSP70 Heat-Shock Proteins
  • fas Receptor
  • L-Lactate Dehydrogenase