Department of Radiation Oncology, Saarland University Medical Center, 66421 Homburg, Saar, Germany.
José Carreras Center, Internal Medicine, Saarland University Medical Center, 66421 Homburg, Saar, Germany.
Int J Mol Sci. 2024 Mar 15;25(6):3320. doi: 10.3390/ijms25063320.
An important hallmark of radiation dermatitis is the impairment of the mitotic ability of the stem/progenitor cells in the basal cell layers due to radiation-induced DNA damage, leading to suppressed cell renewal in the epidermis. However, this mechanism alone does not adequately explain the complex pathogenesis of radiation-induced skin injury. In this review, we summarize the latest findings on the complex pathogenesis of radiation dermatitis and correlate these with the clinical features of radiation-induced skin reactions. The current studies show that skin exposure to ionizing radiation induces cellular senescence in the epidermal keratinocytes. As part of their epithelial stress response, these senescent keratinocytes secrete pro-inflammatory mediators, thereby triggering skin inflammation. Keratinocyte-derived cytokines and chemokines modulate intercellular communication with the immune cells, activating skin-resident and recruiting skin-infiltrating immune cells within the epidermis and dermis, thereby orchestrating the inflammatory response to radiation-induced tissue damage. The increased expression of specific chemoattractant chemokines leads to increased recruitment of neutrophils into the irradiated skin, where they release cytotoxic granules that are responsible for the exacerbation of an inflammatory state. Moreover, the importance of IL-17-expressing γδ-T cells to the radiation-induced hyperproliferation of keratinocytes was demonstrated, leading to reactive hyperplasia of the epidermis. Radiation-induced, reactive hyperproliferation of the keratinocytes disturbs the fine-tuned keratinization and cornification processes, leading to structural dysfunction of the epidermal barrier. In summary, in response to ionizing radiation, epidermal keratinocytes have important structural and immunoregulatory barrier functions in the skin, coordinating interacting immune responses to eliminate radiation-induced damage and to initiate the healing process.
放射性皮炎的一个重要特征是由于辐射诱导的 DNA 损伤,导致基底层干细胞/祖细胞的有丝分裂能力受损,从而导致表皮细胞更新受到抑制。然而,仅仅这一机制并不能充分解释放射性皮肤损伤的复杂发病机制。在这篇综述中,我们总结了放射性皮炎复杂发病机制的最新发现,并将其与放射性皮肤反应的临床特征相关联。目前的研究表明,皮肤暴露于电离辐射会诱导表皮角质形成细胞发生细胞衰老。作为其上皮应激反应的一部分,这些衰老的角质形成细胞会分泌促炎介质,从而引发皮肤炎症。角质形成细胞衍生的细胞因子和趋化因子调节与免疫细胞的细胞间通讯,激活表皮和真皮中的皮肤固有免疫细胞和招募皮肤浸润免疫细胞,从而协调对辐射诱导的组织损伤的炎症反应。特定趋化因子的表达增加导致更多的中性粒细胞募集到照射的皮肤中,它们释放细胞毒性颗粒,导致炎症状态的加剧。此外,IL-17 表达的 γδ-T 细胞对辐射诱导的角质形成细胞过度增殖的重要性也得到了证实,导致表皮的反应性增生。辐射诱导的角质形成细胞过度增殖扰乱了精细的角化和角质化过程,导致表皮屏障的结构功能障碍。总之,在电离辐射的作用下,表皮角质形成细胞在皮肤中具有重要的结构和免疫调节屏障功能,协调相互作用的免疫反应,以消除辐射诱导的损伤并启动愈合过程。