The Base of "111 Project" for Biomechanics & Tissue Repair Engineering; Key Laboratory of Biorheological Science and Technology, Ministry of Education, Bioengineering College, Chongqing University, Chongqing 400044, China.
Chongqing Traditional Chinese Medicine Hospital, Chongqing 400011, China.
Oxid Med Cell Longev. 2019 Nov 21;2019:5416728. doi: 10.1155/2019/5416728. eCollection 2019.
Ultraviolet (UV) irradiation can be considered as a double-edged sword: not only is it a crucial environmental factor that can cause skin-related disorders but it can also be used for phototherapy of skin diseases. Inducible heme oxygenase-1 (HO-1) in response to a variety of stimuli, including UV exposure, is vital to maintain cell homeostasis. Heme oxygenase-2 (HO-2), another member of the heme oxygenase family, is constitutively expressed. In this review, we discuss how heme oxygenase (HO), a vital rate-limiting enzyme, participates in heme catabolism and cytoprotection. Phylogenetic analysis showed that there may exist a functional differentiation between HO-1 and HO-2 during evolution. Furthermore, depending on functions in immunomodulation and antioxidation, HO-1 participates in disease progression, especially in pathogenesis of skin diseases, such as vitiligo and psoriasis. To further investigate the particular role of HO-1 in diseases, we summarized the profile of the HO enzyme system and its related signaling pathways, such as Nrf2 and endoplasmic reticulum crucial signaling, both known to regulate HO-1 expression. Furthermore, we report on a C-terminal truncation of HO-1, which is generally considered as a signal molecule. Also, a newly identified alternative splice isoform of HO-1 not only provides us a novel perspective on comprehensive HO-1 alternative splicing but also offers us a basis to clarify the relationship between HO-1 transcripts and oxidative diseases. To conclude, the HO system is not only involved in heme catabolism but also involved in biological processes related to the pathogenesis of certain diseases, even though the mechanism of disease progression still remains sketchy. Further understanding the role of the HO system and its relationship to UV is helpful for revealing the HO-related signaling networks and the pathogenesis of many diseases.
紫外线 (UV) 辐射可以被视为一把双刃剑:它不仅是一种导致皮肤相关疾病的重要环境因素,还可以用于皮肤病的光疗。诱导型血红素加氧酶-1(HO-1)对多种刺激(包括 UV 暴露)做出反应,对于维持细胞内稳态至关重要。血红素加氧酶-2(HO-2)是血红素加氧酶家族的另一个成员,它是组成性表达的。在这篇综述中,我们讨论了血红素加氧酶(HO)这一重要的限速酶如何参与血红素分解代谢和细胞保护。系统发育分析表明,HO-1 和 HO-2 在进化过程中可能存在功能分化。此外,HO-1 还通过免疫调节和抗氧化作用参与疾病的进展,特别是在白癜风和银屑病等皮肤病的发病机制中。为了进一步研究 HO-1 在疾病中的特定作用,我们总结了 HO 酶系统及其相关信号通路的特征,如 Nrf2 和内质网关键信号通路,这些通路都已知可以调节 HO-1 的表达。此外,我们还报告了 HO-1 的 C 端截断,通常被认为是一种信号分子。此外,新发现的 HO-1 替代剪接异构体不仅为我们提供了一个关于 HO-1 替代剪接的全新视角,也为我们阐明 HO-1 转录本与氧化疾病之间的关系提供了依据。总之,HO 系统不仅参与血红素分解代谢,还参与某些疾病发病机制相关的生物学过程,尽管疾病进展的机制仍不明确。进一步了解 HO 系统的作用及其与 UV 的关系有助于揭示与 HO 相关的信号网络和许多疾病的发病机制。