Li Yunlong, Ma Kuai, Han Zhongyu, Chi Mingxuan, Sai Xiyalatu, Zhu Ping, Ding Zhaolun, Song Linjiang, Liu Chi
Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
School of Medical and Life Sciences, Reproductive and Women-Children Hospital, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Front Med (Lausanne). 2021 Aug 24;8:708453. doi: 10.3389/fmed.2021.708453. eCollection 2021.
Kidney disease is a general term for heterogeneous damage that affects the function and the structure of the kidneys. The rising incidence of kidney diseases represents a considerable burden on the healthcare system, so the development of new drugs and the identification of novel therapeutic targets are urgently needed. The pathophysiology of kidney diseases is complex and involves multiple processes, including inflammation, autophagy, cell-cycle progression, and oxidative stress. Heme oxygenase-1 (HO-1), an enzyme involved in the process of heme degradation, has attracted widespread attention in recent years due to its cytoprotective properties. As an enzyme with known anti-oxidative functions, HO-1 plays an indispensable role in the regulation of oxidative stress and is involved in the pathogenesis of several kidney diseases. Moreover, current studies have revealed that HO-1 can affect cell proliferation, cell maturation, and other metabolic processes, thereby altering the function of immune cells. Many strategies, such as the administration of HO-1-overexpressing macrophages, use of phytochemicals, and carbon monoxide-based therapies, have been developed to target HO-1 in a variety of nephropathological animal models, indicating that HO-1 is a promising protein for the treatment of kidney diseases. Here, we briefly review the effects of HO-1 induction on specific immune cell populations with the aim of exploring the potential therapeutic roles of HO-1 and designing HO-1-based therapeutic strategies for the treatment of kidney diseases.
肾脏疾病是一个通用术语,用于描述影响肾脏功能和结构的异质性损伤。肾脏疾病发病率的不断上升给医疗保健系统带来了相当大的负担,因此迫切需要开发新药并确定新的治疗靶点。肾脏疾病的病理生理学很复杂,涉及多个过程,包括炎症、自噬、细胞周期进程和氧化应激。血红素加氧酶-1(HO-1)是一种参与血红素降解过程的酶,近年来因其细胞保护特性而受到广泛关注。作为一种具有已知抗氧化功能的酶,HO-1在氧化应激调节中起着不可或缺的作用,并参与多种肾脏疾病的发病机制。此外,目前的研究表明,HO-1可以影响细胞增殖、细胞成熟和其他代谢过程,从而改变免疫细胞的功能。已经开发了许多策略,如给予过表达HO-1的巨噬细胞、使用植物化学物质和基于一氧化碳的疗法,以在各种肾脏病理动物模型中靶向HO-1,这表明HO-1是一种有前景的治疗肾脏疾病的蛋白质。在此,我们简要综述HO-1诱导对特定免疫细胞群体的影响,旨在探索HO-1的潜在治疗作用,并设计基于HO-1的治疗策略来治疗肾脏疾病。