Cadmium induces chondroitin sulfate synthase 1 via protein kinase Cα and elongates chondroitin/dermatan sulfate chains in cultured vascular endothelial cells

J Toxicol Sci. 2023;48(8):457-467. doi: 10.2131/jts.48.457.

Abstract

Cadmium is an environmental pollutant and a risk factor for atherosclerosis. In the atherosclerotic intima, dermatan sulfate chains accelerate accumulation and oxidation of LDL cholesterol. The major type of dermatan sulfate proteoglycan that is synthesized by vascular endothelial cells is biglycan. In the present study, we analyzed the effect of cadmium on the biglycan synthesis using cultured bovine aortic endothelial cells. Cadmium did not induce biglycan mRNA and core protein expression; however, it elongated the chondroitin/dermatan sulfate chains of biglycan. Among elongation enzymes of the chondroitin/dermatan sulfate chain, chondroitin sulfate synthase 1 (CHSY1) mRNA and protein expression were dose- and time-dependently upregulated by cadmium depending on protein kinase Cα. This finding suggests that CHSY1-dependent elongation of chondroitin/dermatan sulfate chains of biglycan may exacerbate cadmium-induced atherosclerosis.

Keywords: Cadmium; Chondroitin sulfate synthase 1; Chondroitin/dermatan sulfate; Proteoglycan; Vascular endothelial cell.

MeSH terms

  • Animals
  • Biglycan
  • Cadmium
  • Cattle
  • Cells, Cultured
  • Chondroitin Sulfates*
  • Dermatan Sulfate* / metabolism
  • Endothelial Cells / metabolism
  • Protein Kinases
  • RNA, Messenger

Substances

  • Chondroitin Sulfates
  • Biglycan
  • Dermatan Sulfate
  • Cadmium
  • RNA, Messenger
  • Protein Kinases