Zhang Jiahui, Zhang Mingzhuo, Tatar Marc, Gong Rujun
Division of Nephrology, Department of Medicine, University of Toledo College of Medicine, Toledo, OH, USA.
Division of Biology and Medicine, Brown University, Providence, RI, USA.
Redox Biol. 2025 May;82:103593. doi: 10.1016/j.redox.2025.103593. Epub 2025 Mar 12.
The transcription factor NF-E2-related factor 2 (Nrf2) is a master regulator of antioxidant responses in mammals, where it plays a critical role in detoxification, maintaining cellular homeostasis, combating inflammation and fibrosis, and slowing disease progression. Kelch-like ECH-associated protein 1 (Keap1), an adaptor subunit of Cullin 3-based E3 ubiquitin ligase, serves as a critical sensor of oxidative and electrophilic stress, regulating Nrf2 activity by sequestering it in the cytoplasm, leading to its proteasomal degradation and transcriptional repression. However, the clinical potential of targeting the Keap1-dependent Nrf2 regulatory pathway has been limited. This is evidenced by early postnatal lethality in Keap1 knockout mice, as well as significant adverse events after pharmacological blockade of Keap1 in human patients with Alport syndrome as well as in those with type 2 diabetes mellitus and chronic kidney disease. The exact underlying mechanisms remain elusive, but may involve non-specific and systemic activation of the Nrf2 antioxidant response in both injured and normal tissues. Beyond Keap1-dependent regulation, Nrf2 activity is modulated by Keap1-independent mechanisms, including transcriptional, epigenetic, and post-translational modifications. In particular, GSK3β has emerged as a critical convergence point for these diverse signaling pathways. Unlike Keap1-dependent regulation, GSK3β-mediated Keap1-independent Nrf2 regulation does not affect basal Nrf2 activity but modulates its response at a delayed/late phase of cellular stress. This allows fine-tuning of the inducibility, magnitude, and duration of the Nrf2 response specifically in stressed or injured tissues. As one of the most metabolically active organs, the kidney is a major source of production of reactive oxygen and nitrogen species and also a vulnerable organ to oxidative damage. Targeting the GSK3β-mediated Nrf2 regulatory pathway represents a promising new approach for the treatment of kidney disease.
转录因子NF-E2相关因子2(Nrf2)是哺乳动物抗氧化反应的主要调节因子,在解毒、维持细胞内稳态、对抗炎症和纤维化以及减缓疾病进展中发挥关键作用。kelch样ECH相关蛋白1(Keap1)是Cullin 3基E3泛素连接酶的衔接子亚基,作为氧化应激和亲电应激的关键传感器,通过将Nrf2隔离在细胞质中来调节其活性,导致其蛋白酶体降解和转录抑制。然而,靶向Keap1依赖性Nrf2调节途径的临床潜力一直有限。Keap1基因敲除小鼠出生后早期死亡,以及在患有Alport综合征、2型糖尿病和慢性肾病的人类患者中对Keap1进行药物阻断后出现的重大不良事件都证明了这一点。确切的潜在机制仍然难以捉摸,但可能涉及受损组织和正常组织中Nrf2抗氧化反应的非特异性和全身性激活。除了Keap1依赖性调节外,Nrf2的活性还受到Keap1非依赖性机制的调节,包括转录、表观遗传和翻译后修饰。特别是,糖原合成酶激酶3β(GSK3β)已成为这些不同信号通路的关键交汇点。与Keap1依赖性调节不同,GSK3β介导的Keap1非依赖性Nrf2调节不影响基础Nrf2活性,但在细胞应激的延迟/后期调节其反应。这使得能够在应激或受损组织中对Nrf2反应的诱导性、幅度和持续时间进行微调。作为代谢最活跃的器官之一,肾脏是活性氧和氮物种产生的主要来源,也是易受氧化损伤的器官。靶向GSK3β介导的Nrf2调节途径代表了一种有前途的治疗肾脏疾病的新方法。