A Microbiome-Derived Peptide Induces Apoptosis of Cells from Different Tissues

Cells. 2021 Oct 26;10(11):2885. doi: 10.3390/cells10112885.

Abstract

Apoptosis is a programmed cell death involved in embryogenesis and tissue homeostasis under physiological conditions. However, abnormalities in the process of apoptosis are implicated in the pathogenesis of various diseases. The human microbiota may release products that induce apoptosis of host cells. We recently identified a novel microbiome-derived peptide called corisin that worsens lung fibrosis by inducing apoptosis of lung epithelial cells. We hypothesized that corisin and a corisin-like peptide might also induce apoptosis of cells from different tissues. We cultured podocytes, renal tubular epithelial cells, keratinocytes, retinal and intestinal cells treated with corisin and evaluated apoptosis by flow cytometry and Western blotting. Although at different grades, flow cytometry analysis and Western blotting showed that corisin and a corisin-like peptide induced apoptosis of podocytes, keratinocytes, tubular epithelial cells, retinal, and intestinal cells. In addition, we found that corisin synergistically enhances the proapoptotic activity of transforming growth factor-β1 on podocytes. In conclusion, these results suggest that corisin and corisin-like peptides may play a role in the pathogenesis of disease in different organs by promoting apoptosis of parenchymal cells.

Keywords: apoptosis; corisin; different tissue; organ fibrosis; parenchymal cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis* / drug effects
  • Caspase 3 / metabolism
  • Cell Line, Tumor
  • Epithelial Cells / drug effects
  • Epithelial Cells / pathology
  • HaCaT Cells
  • Humans
  • Keratinocytes / drug effects
  • Keratinocytes / pathology
  • Microbiota* / drug effects
  • Mitochondrial Membranes / drug effects
  • Mitochondrial Membranes / metabolism
  • Organ Specificity* / drug effects
  • Peptides / pharmacology*
  • Podocytes / drug effects
  • Podocytes / pathology
  • Reactive Oxygen Species / metabolism
  • Retina / pathology
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Peptides
  • Reactive Oxygen Species
  • Transforming Growth Factor beta1
  • Caspase 3