Lu Chenxi, Liu Yuan, Ren Feifei, Zhang Haoran, Hou Yafang, Zhang Hong, Chen Zhiyong, Du Xia
Institute of Traditional Chinese Medicine, Shaanxi Academy of Traditional Chinese Medicine, Xi'an, China.
J Cell Physiol. 2025 Jan;240(1):e31465. doi: 10.1002/jcp.31465. Epub 2024 Oct 17.
Fibrosis, an aberrant reparative response to tissue injury, involves a disruption in the equilibrium between the synthesis and degradation of the extracellular matrix, leading to its excessive accumulation within normal tissues, and culminating in organ dysfunction. Manifesting in the terminal stages of nearly all chronic ailments, fibrosis carries a high mortality rate and poses a significant threat to human health. Heme oxygenase-1 (HO-1) emerges as an endogenous protective agent, mitigating tissue damage through its antioxidant, anti-inflammatory, and antiapoptotic properties. Numerous studies have corroborated HO-1's potential as a therapeutic target in anti-fibrosis treatment. This review delves into the structural and functional attributes, and the upstream and downstream pathways of HO-1. Additionally, the regulatory networks and mechanisms of HO-1 in cells associated with fibrosis are elucidated. The role of HO-1 in various fibrosis-related diseases is also explored. Collectively, this comprehensive information serves as a foundation for future research and augments the viability of HO-1 as a therapeutic target for fibrosis.
纤维化是对组织损伤的一种异常修复反应,涉及细胞外基质合成与降解平衡的破坏,导致其在正常组织中过度积累,最终导致器官功能障碍。纤维化出现在几乎所有慢性疾病的终末期,死亡率很高,对人类健康构成重大威胁。血红素加氧酶-1(HO-1)作为一种内源性保护剂出现,通过其抗氧化、抗炎和抗凋亡特性减轻组织损伤。大量研究证实了HO-1作为抗纤维化治疗中治疗靶点的潜力。本综述深入探讨了HO-1的结构和功能特性,以及其上游和下游途径。此外,还阐明了HO-1在与纤维化相关的细胞中的调控网络和机制。还探讨了HO-1在各种纤维化相关疾病中的作用。总的来说,这些全面的信息为未来的研究奠定了基础,并增强了HO-1作为纤维化治疗靶点的可行性。