Age-Related Loss of Innate Immune Antimicrobial Function of Dermal Fat Is Mediated by Transforming Growth Factor Beta

    December 2018 in “ Immunity
    Ling‐juan Zhang, Stella Chen, Christian F. Guerrero‐Juarez, Fengwu Li, Yun Tong, Yuqiong Liang, Marc C. Liggins, Xu Chen, Hao Chen, Min Li, Tissa Hata, Ye Zheng, Maksim V. Plikus, Richard L. Gallo
    TLDR Targeting TGFβ can improve skin immunity in older people.
    The study demonstrated that the age-related decline in the antimicrobial function of dermal fat was mediated by Transforming Growth Factor Beta (TGFβ), which inhibited the adipogenic and antimicrobial functions of dermal fibroblasts (dFB). Neonatal skin, rich in adipogenic dFB and immature dermal fat, effectively expressed antimicrobial peptides like cathelicidin, providing protection against Staphylococcus aureus. However, this capacity decreased with age due to increased TGFβ activity, which promoted a fibrotic phenotype. Inhibition of the TGFβ receptor restored these functions in adult mice, enhancing resistance to infection. The findings suggested that targeting TGFβ pathways could potentially improve skin immunity in older individuals by reversing the age-related switch from a pro-adipogenic to a pro-fibrotic state in dFB.
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