Lee Young Mee, Kim Yeon Kyung, Eun Hee Chul, Chung Jin Ho
Department of Dermatology, Seoul National University College of Medicine and Laboratory of Cutaneous Aging Research, Clinical Research Institute, Seoul National University Hospital, 28, Yeongeon-Dong, Chongno-Gu, Seoul 110-744, Korea.
Arch Dermatol Res. 2009 Aug;301(7):523-9. doi: 10.1007/s00403-009-0960-8. Epub 2009 May 23.
S100A8, a calcium-binding protein, is associated with keratinocyte differentiation, inflammation and wound healing. S100A8 is induced by various skin stresses and diseases, which suggests that S100A8 plays a role in those processes. However, it has not been reported how the expression of S100A8 is affected during skin aging or whether S100A8 plays a role in the skin aging process. In this study, we investigated the changes in S100A8 mRNA and protein following acute UV irradiation to human buttock skin and by intrinsic aging and photoaging in human sun-protected (upper-inner arm) and sun-exposed (forearm) skin of elderly subjects. Real-time PCR, western blot and immunohistochemical staining analyses of UV-irradiated young buttock skin revealed that S100A8 protein expression was increased at 24 h (3.0-fold) and 48 h (4.4-fold) after UV irradiation. S100A8 mRNA and protein were more highly expressed by 2.3- and 4.0-fold, respectively, in the sun-protected skin of elderly people than in that of young people. In addition, the sun-exposed skin of elderly expressed more S100A8 mRNA and protein than the sun-protected skin of the same individuals. In immunohistochemical staining, facial (photoaged) skin > or = 72 years showed higher epidermal expression of S100A8 than that of the other age groups. Based on the above results, our data suggest that the expression of S100A8 is affected by acute UV irradiation, intrinsic aging and photoaging processes.
S100A8是一种钙结合蛋白,与角质形成细胞分化、炎症及伤口愈合相关。S100A8由多种皮肤应激和疾病诱导产生,这表明S100A8在这些过程中发挥作用。然而,尚未有关于皮肤衰老过程中S100A8表达如何受到影响,以及S100A8是否在皮肤衰老进程中发挥作用的报道。在本研究中,我们调查了急性紫外线照射人臀部皮肤以及老年受试者防晒(上臂内侧)和暴露于阳光下(前臂)皮肤的自然衰老和光老化后S100A8 mRNA和蛋白的变化。对紫外线照射的年轻臀部皮肤进行实时PCR、蛋白质印迹和免疫组织化学染色分析显示,紫外线照射后24小时(3.0倍)和48小时(4.4倍)S100A8蛋白表达增加。老年人防晒皮肤中S100A8 mRNA和蛋白的表达分别比年轻人高2.3倍和4.0倍。此外,老年人暴露于阳光下的皮肤比同一人群的防晒皮肤表达更多的S100A8 mRNA和蛋白。在免疫组织化学染色中,72岁及以上的面部(光老化)皮肤S100A8的表皮表达高于其他年龄组。基于上述结果,我们的数据表明S100A8的表达受到急性紫外线照射、自然衰老和光老化过程的影响。