N ε-Carboxymethyl-Lysine Negatively Regulates Foam Cell Migration via the Vav1/Rac1 Pathway

J Immunol Res. 2020 Feb 28:2020:1906204. doi: 10.1155/2020/1906204. eCollection 2020.

Abstract

Background: Macrophage-derived foam cells play a central role in atherosclerosis, and their ultimate fate includes apoptosis, promotion of vascular inflammation, or migration to other tissues. Nε-Carboxymethyl-lysine (CML), the key active component of advanced glycation end products, induced foam cell formation and apoptosis. Previous studies have shown that the Vav1/Rac1 pathway affects the macrophage cytoskeleton and cell migration, but its role in the pathogenesis of diabetic atherosclerosis is unknown.

Methods and results: In this study, we used anterior tibiofibular vascular samples from diabetic foot amputation patients and accident amputation patients, and histological and cytological tests were performed using a diabetic ApoE-/- mouse model and primary peritoneal macrophages, respectively. The results showed that the atherosclerotic plaques of diabetic foot amputation patients and diabetic ApoE-/- mice were larger than those of the control group. Inhibition of the Vav1/Rac1 pathway reduced vascular plaques and promoted the migration of macrophages to lymph nodes. Transwell and wound healing assays showed that the migratory ability of macrophage-derived foam cells was inhibited by CML. Cytoskeletal staining showed that advanced glycation end products inhibited the formation of lamellipodia in foam cells, and inhibition of the Vav1/Rac1 pathway restored the formation of lamellipodia.

Conclusion: CML inhibits the migration of foam cells from blood vessels via the Vav1/Rac1 pathway, and this process affects the formation of lamellipodia.

MeSH terms

  • Amputation, Surgical
  • Animals
  • Apolipoproteins E / genetics
  • Apolipoproteins E / metabolism*
  • Atherosclerosis / metabolism*
  • Atherosclerosis / pathology
  • Cell Movement
  • Cells, Cultured
  • Diabetic Foot / metabolism*
  • Diabetic Foot / pathology
  • Foam Cells / physiology*
  • Humans
  • Lysine / analogs & derivatives*
  • Lysine / metabolism
  • Mice
  • Mice, Knockout
  • Proto-Oncogene Proteins c-vav / metabolism*
  • Signal Transduction
  • rac1 GTP-Binding Protein / metabolism*

Substances

  • Apolipoproteins E
  • Proto-Oncogene Proteins c-vav
  • Vav1 protein, mouse
  • N(6)-carboxymethyllysine
  • rac1 GTP-Binding Protein
  • Lysine