Discipline of Dermatology, Bosch Institute, University of Sydney, Camperdown, NSW, Australia.
Immune Imaging Program, Centenary Institute for Cancer Medicine and Cell Biology, Camperdown, NSW, Australia.
Photochem Photobiol. 2017 Jul;93(4):920-929. doi: 10.1111/php.12686. Epub 2017 Feb 28.
The cornea sits at the anterior aspect of the eye and, like the skin, is highly exposed to ultraviolet radiation (UVR). The cornea blocks a significant proportion of UVB from reaching the posterior structures of the eye. However, UVA can penetrate the full thickness of the cornea, even reaching the anterior portion of the lens. Epidemiological data indicate that UVR is a contributing factor for a multitude of diseases of the cornea including pterygium, photokeratitis, climatic droplet keratopathy and ocular surface squamous neoplasia (OSSN), although the pathogenic mechanisms of each require further elucidation. UVR is a well-known genotoxic agent, and its effects have been well characterized in organs such as the skin. However, we are only beginning to identify its effects on the cornea, such as the UVR signature C → T and CC → TT transversions identified by sequencing and increased proliferative and shedding rates in response to UVR exposure. Alarmingly, a single low-dose exposure of UVR to the cornea is sufficient to elicit genetic, molecular and cellular changes, supporting the consideration of using protective measures, such as wearing sunglasses when outdoors. The aim of this review was to describe the adverse effects of UVR on the cornea.
角膜位于眼睛的前表面,像皮肤一样,高度暴露于紫外线辐射 (UVR) 之下。角膜可阻止相当一部分 UVB 到达眼睛的后部结构。然而,UVA 可以穿透角膜的全部厚度,甚至到达晶状体的前部。流行病学数据表明,UVR 是多种角膜疾病的一个致病因素,包括翼状胬肉、光性角膜炎、气候性滴状角膜病变和眼表鳞状上皮肿瘤 (OSSN),尽管每种疾病的发病机制都需要进一步阐明。UVR 是一种众所周知的遗传毒性物质,其在皮肤等器官中的作用已得到充分描述。然而,我们才刚刚开始识别其对角膜的影响,例如通过测序确定的 UVR 特征性 C → T 和 CC → TT 颠换,以及对 UVR 暴露的增殖和脱落率增加。令人震惊的是,单次低剂量的 UVR 暴露就足以引起角膜的遗传、分子和细胞变化,这支持了考虑采取保护措施的观点,例如在户外活动时戴太阳镜。本综述的目的是描述 UVR 对角膜的不良影响。