Center for Cancer Immunology, Massachusetts General Hospital, Boston, Massachusetts, USA; Cutaneous Biology Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA; Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA; Harvard Medical School, Boston, Massachusetts, USA.
Shiseido Global Innovation Center, Yokohama, Japan.
J Invest Dermatol. 2020 Jul;140(7):1327-1334. doi: 10.1016/j.jid.2019.11.017. Epub 2019 Dec 25.
The skin provides the first line of physical and immunological defense against environmental insults. However, the age-related changes in the immune function of human skin are unclear. Here, we investigated the age-related changes in epidermal Langerhans cells (LCs), which play a sentinel role in the initiation of the immune responses in the skin. We found a significant reduction in the number of epidermal LCs in sun-protected skin with age. Among the possible explanations for this reduction, the number of CD14 CD207 CCR6 dermal-resident monocytes that can differentiate into epidermal LCs was markedly reduced with age (P = 0.0057). Among the chemokines that can recruit these cells into the skin, the expression of CXCL14 was significantly down-regulated in epidermal keratinocytes with age. In addition, we discovered that young skin recruited a significantly higher number of monocytic THP-1 cells compared with old skin ex vivo. This recruitment was blocked by CXCL14 neutralizing antibody and conversely promoted by CXCL14 treatment. Collectively, our findings indicate that decreased CXCL14-mediated recruitment of CD14 monocytes in human skin results in the reduction of epidermal LCs with age, and CXCL14 may provide a therapeutic target for the prevention of age-related reduction in LCs.
皮肤是人体抵御环境侵害的第一道生理和免疫防线。然而,目前尚不清楚人类皮肤的免疫功能随年龄增长而发生的变化。在这里,我们研究了表皮朗格汉斯细胞(LCs)随年龄的变化,LCs 在皮肤免疫反应的启动中起哨兵作用。我们发现,随着年龄的增长,在防晒皮肤中表皮 LCs 的数量显著减少。在这种减少的可能解释中,能够分化为表皮 LCs 的 CD14 CD207 CCR6 真皮常驻单核细胞的数量随着年龄的增长而明显减少(P=0.0057)。在可以招募这些细胞进入皮肤的趋化因子中,表皮角质形成细胞中 CXCL14 的表达随年龄增长显著下调。此外,我们发现与老年皮肤相比,年轻皮肤在体外可招募数量显著更多的单核细胞 THP-1 细胞。这种募集被 CXCL14 中和抗体阻断,而 CXCL14 处理则促进了募集。总之,我们的研究结果表明,人类皮肤中 CXCL14 介导的 CD14 单核细胞募集减少导致表皮 LCs 随年龄增长而减少,而 CXCL14 可能为预防 LCs 随年龄增长而减少提供治疗靶点。