Monasterium Laboratory GmbH, Muenster, Germany.
Mediteknia Skin & Hair Lab, Universidad Fernando Pessoa Canarias, and Medical Pathology Group, IUIBS, Universidad de Las Palmas de Gran Canaria, Las Palmas, Spain.
Int J Cosmet Sci. 2019 Apr;41(2):164-182. doi: 10.1111/ics.12521.
Although the effect of ultraviolet radiation (UVR) on human skin has been extensively studied, very little is known on how UVR impacts on hair follicle (HF) homeostasis. Here, we investigated how solar spectrum UVR that hits the human skin surface impacts on HF biology, and whether any detrimental effects can be mitigated by a widely used cosmetic and nutraceutical ingredient, caffeine.
Human scalp skin with terminal HFs was irradiated transepidermally ex vivo using either 10 J/cm UVA (340-440 nm) + 20 mJ/cm UVB (290-320 nm) (low dose) or 50 J/cm UVA + 50 mJ/cm UVB (high dose) and organ-cultured under serum-free conditions for 1 or 3 days. 0.1% caffeine (5.15 mmol/L) was topically applied for 3 days prior to UV exposure with 40 J/cm UVA + 40 mJ/cm UVB and for 3 days after UVR. The effects on various toxicity and vitality read-out parameters were measured in defined skin and HF compartments.
Consistent with previous results, transepidermal UVR exerted skin cytotoxicity and epidermal damage. Treatment with high and/or low UVA+UVB doses also induced oxidative DNA damage and cytotoxicity in human HFs. In addition, it decreased proliferation and promoted apoptosis of HF outer root sheath (ORS) and hair matrix (HM) keratinocytes, stimulated catagen development, differentially regulated the expression of HF growth factors, and induced perifollicular mast cell degranulation. UVR-mediated HF damage was more severe after irradiation with high UVR dose and reached also proximal HF compartments. The topical application of 0.1% caffeine did not induce skin or HF cytotoxicity and stimulated the expression of IGF-1 in the proximal HF ORS. However, it promoted keratinocyte apoptosis in selected HF compartments. Moreover, caffeine provided protection towards UVR-mediated HF cytotoxicity and dystrophy, keratinocyte apoptosis, and tendential up-regulation of the catagen-promoting growth factor.
Our study highlights the clinical relevance of our scalp UV irradiation ex vivo assay and provides the first evidence that transepidermal UV radiation negatively affects important human HF functions. This suggests that it is a sensible prophylactic strategy to integrate agents such as caffeine that can act as HF photoprotectants into sun-protective cosmeceutical and nutraceutical formulations.
尽管紫外线(UVR)对人类皮肤的影响已得到广泛研究,但对于 UVR 如何影响毛囊(HF)稳态知之甚少。在这里,我们研究了到达人类皮肤表面的太阳光谱 UVR 如何影响 HF 生物学,以及广泛使用的化妆品和营养成分咖啡因是否可以减轻任何有害影响。
使用 10 J/cm UVA(340-440nm)+20 mJ/cm UVB(290-320nm)(低剂量)或 50 J/cm UVA+50 mJ/cm UVB(高剂量)经表皮体外辐照人头皮带终末 HF 的皮肤,并在无血清条件下器官培养 1 或 3 天。在接受 40 J/cm UVA+40 mJ/cm UVB 照射之前和之后的 3 天内,将 0.1%咖啡因(5.15mmol/L)局部应用于皮肤 3 天。测量各种毒性和活力读数参数在定义的皮肤和 HF 隔室中的影响。
与之前的结果一致,经表皮 UVR 会导致皮肤细胞毒性和表皮损伤。高剂量和/或低剂量 UVA+UVB 处理还会诱导人 HF 中的氧化 DNA 损伤和细胞毒性。此外,它会降低 HF 外根鞘(ORS)和毛基质(HM)角质形成细胞的增殖并促进其凋亡,刺激毛囊退化的发生,差异调节 HF 生长因子的表达,并诱导毛囊周围肥大细胞脱颗粒。用高 UVR 剂量照射后,HF 损伤更为严重,甚至累及近端 HF 隔室。0.1%咖啡因的局部应用不会引起皮肤或 HF 细胞毒性,并刺激近端 HF ORS 中 IGF-1 的表达。然而,它会促进选定 HF 隔室中的角质形成细胞凋亡。此外,咖啡因可提供针对 UVR 介导的 HF 细胞毒性和营养不良、角质形成细胞凋亡以及倾向于上调促进毛发生长的生长因子的保护作用。
我们的研究强调了我们的头皮体外 UV 照射测定的临床相关性,并首次证明经表皮紫外线辐射会对重要的人类 HF 功能产生负面影响。这表明,将咖啡因等可作为 HF 光保护剂的物质整合到防晒化妆品和营养保健品配方中,是一种明智的预防策略。