Li Duo, Wei Ting-Ting, Cai Jiping, Xie Tian-Hua, Yao Yong, Zhu Lingpeng
Department of Ophthalmology, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, Jiangsu Province, China; Wuxi Medical Center, Nanjing Medical University, Wuxi, Jiangsu Province, China.
Wuxi Medical Center, Nanjing Medical University, Wuxi, Jiangsu Province, China; Center of Clinical Research, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, Jiangsu Province, China.
Exp Eye Res. 2023 Aug;233:109549. doi: 10.1016/j.exer.2023.109549. Epub 2023 Jun 20.
Smad ubiquitylation regulatory factor-1 (Smurf1) is one of C2-WW-HECT domain E3 ubiquitin ligases, it can regulate BMP pathway by mediating ubiquitylation degradation of Smad1/Smad5. Many functions about Smurf1 also are still unknown, especially in retina. This research is about to explore the role of Smurf1 in retina degeneration. Tail vein injection of sodium iodate (NaIO) in C57BL/6J mice was the animal model of retina degeneration. In NaIO model, Smurf1 had more expression than normal mice. Specific Smurf1 inhibitor, A01, was injected into vitreous cavity. Results showed that inhibiting Smurf1 could alleviate acute retina injury, such as keeping a better retina structure in living imaging and histologic sections, less cell death and inflammation activation. Tert-butyl hydroperoxide (TBH) was used to establish oxidative stress injury in human retinal pigments epithelial cell line (ARPE-19). Oxidative stress injury gradually caused co-upregulation of Smurf1, TGF-β1 and phosphorylated NF-κB (pNF-κB). TGF-β1 could directly induce Smurf1 expression. Inhibiting Smurf1 had an anti-epithelial mesenchymal transition (anti-EMT) function. Similarly, A01 also could inhibit the expression of pNF-κB, NLRP3 and IL-1β. At last, after searching bioinformatics database, Smurf1 had a possible interaction with beta-transducin repeat containing E3 ubiquitin protein ligase (β-TrCP), another E3 ubiquitin ligases. β-TrCP can mediate ubiquitination degradation of p-IκBα. Lentivirus-SMURF1 was used to overexpress Smurf1, and GS143 was used to inhibit β-TrCP. The results showed Smurf1 could directly induce NF-κB, pNF-κB, and NLRP3 expression, and keep a stable β-TrCP expression. However, inhibiting β-TrCP could cause more NF-κB activation and NLRP3 expression. Therefore, β-TrCP may play a negative role in NF-κB pathway activation. In summary, Smurf1 plays a role in exacerbating oxidative stress injury and inflammation in retina and may become a potential therapeutic target in ROS injury of retina.
Smad泛素化调节因子1(Smurf1)是C2-WW-HECT结构域E3泛素连接酶之一,它可通过介导Smad1/Smad5的泛素化降解来调节骨形态发生蛋白(BMP)信号通路。关于Smurf1的许多功能仍不清楚,尤其是在视网膜中。本研究旨在探索Smurf1在视网膜变性中的作用。给C57BL/6J小鼠尾静脉注射碘酸钠(NaIO)作为视网膜变性的动物模型。在NaIO模型中,Smurf1的表达高于正常小鼠。将特异性Smurf1抑制剂A01注入玻璃体腔。结果显示,抑制Smurf1可减轻急性视网膜损伤,如在活体成像和组织学切片中保持更好的视网膜结构,减少细胞死亡和炎症激活。用叔丁基过氧化氢(TBH)在人视网膜色素上皮细胞系(ARPE-19)中建立氧化应激损伤。氧化应激损伤逐渐导致Smurf1、转化生长因子-β1(TGF-β1)和磷酸化核因子-κB(pNF-κB)共同上调。TGF-β1可直接诱导Smurf1表达。抑制Smurf1具有抗上皮-间质转化(抗EMT)功能。同样,A01也可抑制pNF-κB、NLRP3和白细胞介素-1β(IL-1β)的表达。最后,在检索生物信息学数据库后,发现Smurf1可能与另一种E3泛素连接酶——含β-转导蛋白重复序列的E3泛素蛋白连接酶(β-TrCP)相互作用。β-TrCP可介导p-IκBα的泛素化降解。使用慢病毒-SMURF1过表达Smurf1,使用GS143抑制β-TrCP。结果显示,Smurf1可直接诱导核因子-κB(NF-κB)、pNF-κB和NLRP3表达,并维持β-TrCP表达稳定。然而,抑制β-TrCP可导致更多的NF-κB激活和NLRP3表达。因此,β-TrCP可能在NF-κB信号通路激活中起负性作用。综上所述,Smurf1在加重视网膜氧化应激损伤和炎症中起作用,可能成为视网膜活性氧损伤的潜在治疗靶点。