Elastin-derived peptide VGVAPG affects the proliferation of mouse cortical astrocytes with the involvement of aryl hydrocarbon receptor (Ahr), peroxisome proliferator-activated receptor gamma (Pparγ), and elastin-binding protein (EBP)

Cytokine. 2020 Feb:126:154930. doi: 10.1016/j.cyto.2019.154930. Epub 2019 Nov 21.

Abstract

During aging and ischemic and hemorrhagic stroke, elastin molecules are degraded and elastin-derived peptides are released into the brain microenvironment. Val-Gly-Val-Ala-Pro-Gly (VGVAPG) is a repeating hexapeptide in the elastin molecule. It is well documented that the peptide sequence binds with high affinity to elastin-binding protein (EBP) located on the cell surface, thereby transducing a molecular signal into the cell. The aim of our study was to investigate whether EBP, aryl hydrocarbon receptor (Ahr), and peroxisome proliferator-activated receptor gamma (Pparγ) are involved in VGVAPG-stimulated proliferation. Primary astrocytes were maintained in DMEM/F12 medium without phenol red, supplemented with 10 or 1% charcoal/dextran-treated fetal bovine serum (FBS). The cells were exposed to increasing concentrations of VGVAPG peptide, and resazurin reduction was measured. In addition, Glb1, Pparγ, and Ahr genes were silenced. After 48 h of exposure to 10 nM and 1 µM of VGVAPG peptide, the level of estradiol (E2) and the expression of Ki67 and S100B proteins were measured. The results showed that at a wide range of concentrations, VGVAPG peptide increased the metabolism of astrocytes depending on the concentration of FBS. After silencing of Glb1, Pparγ, and Ahr genes, VGVAPG peptide did not affect the cell metabolism which suggests the involvement of all the mentioned receptors in its mechanism of action. Interestingly, in the low-FBS medium, the silencing of Glb1 gene did not result in complete inhibition of VGVAPG-stimulated proliferation. On the other hand, in the medium with 10% FBS VGVAPG increased Ki67 expression after Pparγ silencing, whereas in the medium with 1% FBS VGVAPG decreased Ki67 expression. Following the application of Ahr siRNA, VGVAPG peptide decreased the production of E2 and increased the expression of Ki67 and S100B proteins.

Keywords: Astrocyte; Elastin-derived peptides; Pparγ; Proliferation; VGVAPG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / metabolism*
  • Cell Proliferation / physiology
  • Cells, Cultured
  • Elastin / metabolism*
  • Estradiol / blood
  • Female
  • Ki-67 Antigen / metabolism
  • Mice
  • Oligopeptides / metabolism*
  • Oxazines / metabolism
  • PPAR gamma / genetics
  • PPAR gamma / metabolism*
  • Pregnancy
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Receptors, Aryl Hydrocarbon / genetics
  • Receptors, Aryl Hydrocarbon / metabolism*
  • Receptors, Cell Surface / metabolism*
  • S100 Calcium Binding Protein beta Subunit / metabolism
  • Xanthenes / metabolism

Substances

  • Ki-67 Antigen
  • Oligopeptides
  • Oxazines
  • PPAR gamma
  • Pparg protein, mouse
  • RNA, Small Interfering
  • Receptors, Aryl Hydrocarbon
  • Receptors, Cell Surface
  • S100 Calcium Binding Protein beta Subunit
  • S100b protein, mouse
  • Xanthenes
  • elastin-binding proteins
  • resazurin
  • Estradiol
  • Elastin
  • valyl-glycyl-valyl-alanyl-prolyl-glycine