Vitamin D3 inhibits p38 MAPK and senescence-associated inflammatory mediator secretion by senescent fibroblasts that impacts immune responses during ageing

Aging Cell. 2024 Apr;23(4):e14093. doi: 10.1111/acel.14093. Epub 2024 Jan 29.

Abstract

Vitamin D3 replacement in older insufficient adults significantly improves their antigen-specific varicella zoster virus (VZV) cutaneous immunity. However, the mechanisms involved in this enhancement of cutaneous immunity are not known. Here, we show for the first time that vitamin D3 blocks the senescence-associated secretory phenotype (SASP) production by senescent fibroblasts by partially inhibiting the p38 MAPK pathway. Furthermore, transcriptomic analysis of skin biopsies from older subjects after vitamin D3 supplementation shows that vitamin D3 inhibits the same inflammatory pathways in response to saline as the specific p38 inhibitor, losmapimod, which also enhances immunity in the skin of older subjects. Vitamin D3 supplementation therefore may enhance immunity during ageing in part by blocking p38 MAPK signalling and in turn inhibit SASP production from senescent cells in vivo.

Keywords: SASP; ageing; p38 MAPK; senescence; skin; vitamin D.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aging
  • Cellular Senescence* / genetics
  • Cholecalciferol* / metabolism
  • Cholecalciferol* / pharmacology
  • Fibroblasts / metabolism
  • Humans
  • Immunity
  • Inflammation Mediators / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Cholecalciferol
  • p38 Mitogen-Activated Protein Kinases
  • Inflammation Mediators