Peptidomics analysis revealed that a novel peptide VMP‑19 protects against Ang II‑induced injury in human umbilical vein endothelial cells

Mol Med Rep. 2021 Apr;23(4):298. doi: 10.3892/mmr.2021.11937. Epub 2021 Mar 2.

Abstract

Vascular endothelial dysfunction is a vital pathological change in hypertension, which is mainly caused by apoptosis and oxidative stress injury of vascular endothelial cells. Peptidomics is a method for the direct analysis of small bioactive peptides in various biological samples using liquid chromatography‑mass spectrometry (MS)/MS. Given the advantages of the low molecular weight, optimum targeting and easy access to cells, peptides have attracted extensive attention in the field of drug research. However, to the best of our knowledge, little is currently known regarding the role of peptides in vascular endothelial injury. In order to investigate the peptides involved in vascular endothelial protection, MS was used to analyze the peptide profiles in the supernatant of human umbilical vein endothelial cells (HUVECs) stimulated by Ang II. The results revealed that 211 peptides were identified, of which six were upregulated and 13 were downregulated when compared with the control group. Subsequently, the present study analyzed the physical and chemical properties and biological functions of identified peptides by bioinformatics, and successfully screened a peptide (LLQDSVDFSLADAINTEFK) named VMP‑19 that could alleviate the apoptosis and oxidative stress injury of HUVECs induced by Ang II. In conclusion, to the best of our knowledge, the present study was the first to use peptidomics to analyze the peptide profiles of supernatant secreted by HUVECs, and revealed that the novel peptide VMP‑19 could protect HUVECs from apoptosis and oxidative stress injury. The results of the present study could provide novel insights into treatment strategies for hypertension.

Keywords: human umbilical vein endothelial cells; peptidomics; vascular endothelial injury; peptide VMP‑19; apoptosis; oxidative stress.

MeSH terms

  • Amino Acid Sequence
  • Angiotensin II / pharmacology*
  • Apoptosis / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chromatography, Liquid / methods
  • Computational Biology / methods
  • Dose-Response Relationship, Drug
  • Human Umbilical Vein Endothelial Cells / drug effects*
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Oxidative Stress / drug effects
  • Peptides / analysis*
  • Peptides / isolation & purification
  • Peptides / pharmacology
  • Proteomics / methods*
  • Reactive Oxygen Species / metabolism
  • Tandem Mass Spectrometry / methods

Substances

  • Peptides
  • Reactive Oxygen Species
  • Angiotensin II

Grants and funding

The present study was funded by the Health Commission of Changning District, Shanghai, China (grant no. YXMZK009) and the National Natural Science Foundation of China (grant no. 81873540).