Changes in the amount of nucleotide sugars in aged mouse tissues

Glycobiology. 2024 Apr 24;34(6):cwae032. doi: 10.1093/glycob/cwae032.

Abstract

Aging affects tissue glycan profiles, which may alter cellular functions and increase the risk of age-related diseases. Glycans are biosynthesized by glycosyltransferases using the corresponding nucleotide sugar, and the availability of nucleotide sugars affects glycosylation efficiency. However, the effects of aging on nucleotide sugar profiles and contents are yet to be elucidated. Therefore, this study aimed to investigate the effects of aging on nucleotide sugars using a new LC-MS/MS method. Specifically, the new method was used to determine the nucleotide sugar contents of various tissues (brain, liver, heart, skeletal muscle, kidney, lung, and colon) of male C57BL/6NCr mice (7- or 26-month-old). Characteristic age-associated nucleotide sugar changes were observed in each tissue sample. Particularly, there was a significant decrease in UDP-glucuronic acid content in the kidney of aged mice and a decrease in the contents of several nucleotide sugars, including UDP-N-acetylgalactosamine, in the brain of aged mice. Additionally, there were variations in nucleotide sugar profiles among the tissues examined regardless of the age. The kidneys had the highest concentration of UDP-glucuronic acid among the seven tissues. In contrast, the skeletal muscle had the lowest concentration of total nucleotide sugars among the tissues; however, CMP-N-acetylneuraminic acid and CDP-ribitol were relatively enriched. Conclusively, these findings may contribute to the understanding of the roles of glycans in tissue aging.

Keywords: LC-MS; aging; mouse; nucleotide sugar; tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging* / metabolism
  • Animals
  • Brain / metabolism
  • Kidney / chemistry
  • Kidney / metabolism
  • Liver / chemistry
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Muscle, Skeletal / chemistry
  • Muscle, Skeletal / metabolism
  • Nucleotides* / analysis
  • Nucleotides* / metabolism
  • Tandem Mass Spectrometry

Substances

  • Nucleotides