Vitamin D 3 inhibits p38 MAPK and senescence-associated inflammatory mediator secretion by senescent fibroblasts that impacts immune responses during ageing.
Souraya SayeghCarlos Henrique FantecellePhatthamon LaphanuwatPriya SubramanianMalcom H A RustinDaniel C O GomesArne N AkbarEmma S ChambersPublished in: Aging cell (2024)
Vitamin D 3 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 D 3 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 D 3 supplementation shows that vitamin D 3 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 D 3 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.
Keyphrases
- immune response
- community dwelling
- physical activity
- middle aged
- dna damage
- oxidative stress
- induced apoptosis
- endothelial cells
- extracellular matrix
- signaling pathway
- wound healing
- single cell
- sensitive detection
- cell cycle arrest
- stress induced
- cell proliferation
- rna seq
- living cells
- endoplasmic reticulum stress
- ultrasound guided
- quantum dots
- fluorescent probe