CNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007, Lyon, France.
Claude Bernard University Lyon 1, 69100, Villeurbanne, France.
Geroscience. 2024 Aug;46(4):3567-3580. doi: 10.1007/s11357-023-00981-5. Epub 2023 Oct 19.
Sensing temperature is vitally important to adapt our body to environmental changes. Local warm detection is required to initiate regulation of cutaneous blood flow, which is part of the peripheral thermoregulatory mechanisms, and thus avoid damage to surrounding tissues. The mechanisms mediating cutaneous vasodilation during local heat stress are impaired with aging. However, the impact of aging on the ability of the skin to detect subtle thermal changes is unknown. Among heat-activated cation channels, transient receptor potential vanilloid 3 (TRPV3) is a thermo-sensor predominantly expressed on keratinocytes and involved in local vascular thermoregulatory mechanisms of the skin in young mice. In the present study, using a murine in vivo model of local heat exposure of the skin, we showed that heat-induced vasodilation was reduced in old mice associated with reduced expression of TRPV3 channels. We also found a decrease in expression and activity of TRPV3 channel, as well as reduced TRPV3-dependent adenosine tri-phosphate release in human primary keratinocytes from old donors. This study shows that aging alters the epidermal TRPV3 channels, which might delay the detection of changes in skin temperature, thereby limiting the mechanisms triggered for local vascular thermoregulation in the old skin.
感知温度对于我们的身体适应环境变化至关重要。局部热检测对于启动皮肤血流调节是必需的,这是外周体温调节机制的一部分,从而避免周围组织受损。随着年龄的增长,介导局部热应激时皮肤血管扩张的机制受损。然而,年龄对皮肤检测细微热变化能力的影响尚不清楚。在热激活阳离子通道中,瞬时受体电位香草醛 3 (TRPV3) 主要表达于角质形成细胞,参与年轻小鼠皮肤的局部血管体温调节机制。在本研究中,我们使用了一种局部皮肤热暴露的小鼠体内模型,结果表明,热诱导的血管扩张在老年小鼠中减少,与 TRPV3 通道表达减少有关。我们还发现,老年供体的人原代角质形成细胞中 TRPV3 通道的表达和活性降低,以及 TRPV3 依赖性三磷酸腺苷释放减少。这项研究表明,衰老改变了表皮 TRPV3 通道,这可能会延迟对皮肤温度变化的检测,从而限制老年皮肤中触发的局部血管体温调节机制。