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维生素 D 通过抑制衰老成纤维细胞中 p38MAPK 和衰老相关炎症介质的分泌,影响衰老过程中的免疫反应。

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

机构信息

Division of Medicine, University College London, London, UK.

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

出版信息

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

Abstract

Vitamin D 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 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 supplementation shows that vitamin D 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 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.

摘要

在老年维生素 D 不足的成年人中进行维生素 D 替代治疗可显著改善其水痘带状疱疹病毒(VZV)的抗原特异性皮肤免疫。然而,目前尚不清楚这种皮肤免疫增强的机制。在这里,我们首次表明,维生素 D 通过部分抑制 p38 MAPK 通路来阻断衰老相关分泌表型(SASP)的产生。此外,对接受维生素 D 补充后的老年受试者皮肤活检的转录组分析表明,维生素 D 抑制了与生理盐水相同的炎症途径,就像特异性 p38 抑制剂洛马司他一样,这也增强了老年受试者的皮肤免疫。因此,维生素 D 补充可能部分通过阻断 p38 MAPK 信号传导来增强衰老过程中的免疫,并进而抑制体内衰老细胞的 SASP 产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b901/11019144/23f301432031/ACEL-23-e14093-g002.jpg

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