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

Author:

Sayegh Souraya1ORCID,Fantecelle Carlos H.2,Laphanuwat Phatthamon1,Subramanian Priya1,Rustin Malcom H. A.3,Gomes Daniel O.2,Akbar Arne N.1ORCID,Chambers Emma S.4ORCID

Affiliation:

1. Division of Medicine University College London London UK

2. Núcleo de Doenças Infecciosas Universidade Federal do Espírito Santo Vitoria Brazil

3. Department of Dermatology Royal Free Hospital London UK

4. Centre for Immunobiology, Blizard Institute Queen Mary University of London London UK

Abstract

AbstractVitamin 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.

Funder

LEO Fondet

Medical Research Foundation

British Skin Foundation

Barts Charity

Publisher

Wiley

Subject

Cell Biology,Aging

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