Variations in metabolic enzymes cause differential changes of heparan sulfate and hyaluronan in high glucose treated cells on chip

Int J Biol Macromol. 2023 Dec 31;253(Pt 1):126627. doi: 10.1016/j.ijbiomac.2023.126627. Epub 2023 Sep 1.

Abstract

Glycocalyx dysfunction is believed as the first step in diabetic vascular disease. However, few studies have systematically investigated the influence of HG on the glycocalyx as a whole and its major constituent glycans towards one type of cell. Furthermore, most studies utilized traditional two-dimensional (2D) cultures in vitro, which can't provide the necessary fluid environment for glycocalyx. Here, we utilized vascular glycocalyx on chips to evaluate the changes of glycocalyx and its constituent glycans in HG induced HUVECs. Fluorescence microscopy showed up-regulation of hyaluronan (HA) but down-regulation of heparan sulfate (HS). By analyzing the metabolic enzymes of both glycans, a decrease in the ratio of synthetic/degradative enzymes for HA and an increase in that for HS were demonstrated. Two substrates (UDP-GlcNAc, UDP-GlcA) for the synthesis of both glycans were increased according to omics analysis. Since they were firstly pumped into Golgi apparatus to synthesize HS, less substrates may be left for HA synthesis. Furthermore, the differential changes of HA and HS were confirmed in vessel slides from db/db mice. This study would deepen our understanding of impact of HG on glycocalyx formation and diabetic vascular disease.

Keywords: Heparan sulfate; High glucose; Hyaluronan; Microfluidic chip.

MeSH terms

  • Animals
  • Diabetic Angiopathies*
  • Glucose
  • Heparitin Sulfate / metabolism
  • Hyaluronic Acid* / metabolism
  • Mice
  • Uridine Diphosphate

Substances

  • Hyaluronic Acid
  • Heparitin Sulfate
  • Glucose
  • Uridine Diphosphate