Liu Yuan-Fei, Li Fan, Xu Cheng-Yun, Chen Yan, Tu Wei-Ping, Huang Chong
Department of Emergency, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi Province, China.
Department of Nephrology, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi Province, China.
FASEB J. 2025 Apr 15;39(7):e70509. doi: 10.1096/fj.202403024R.
Ischemia-reperfusion (I/R) injury is a significant factor in the development of acute kidney injury (AKI), particularly in clinical scenarios, such as kidney transplantation, cardiac surgery, and severe hypotension. Autophagy, a critical process that eliminates damaged cellular components, has been shown to mitigate I/R injury by reducing oxidative stress and enhancing cell survival. However, when autophagy is disrupted, it can exacerbate kidney damage. Elucidating the role of autophagy in I/R injury is essential for uncovering the molecular mechanisms driving AKI and could facilitate the development of autophagy-based therapies. Protein expression levels were analyzed through western blot, immunohistochemistry (IHC), and immunofluorescence (IF) staining techniques. Interactions between SIRT4, SETDB1, and CBX3 were explored using chromatin immunoprecipitation (ChIP), sequential ChIP (ChIP-reChIP), and co-immunoprecipitation (Co-IP) assays. The association between SIRT4 and PTEN was also examined via Co-IP. Transmission electron microscopy (TEM) was employed to visualize autophagosomes. Furthermore, an in vivo rat model of I/R injury was developed for validation of the findings. Sirtuin 4 (SIRT4) expression was reduced, and autophagy was impaired during I/R injury. Moreover, SIRT4 interacted with phosphatase and tensin homolog (PTEN) to regulate its expression. Furthermore, SET domain bifurcated histone lysine methyltransferase 1 (SETDB1) mediated histone H3 lysine 9 trimethylation (H3K9me3) modifications and recruited chromobox protein homolog 3 (CBX3) to the SIRT4 promoter, leading to the repression of SIRT4 expression in kidney proximal tubular cells. Importantly, SETDB1 knockdown upregulated SIRT4, decreased PTEN expression, promoted autophagy, and protected rats against I/R injury in vivo. SETDB1 recruits CBX3 to regulate the SIRT4/PTEN axis, inhibiting autophagy and promoting I/R-induced kidney injury. These results suggest that targeting the SETDB1-SIRT4 axis could offer a novel therapeutic strategy to mitigate renal damage in I/R-induced AKI.
缺血再灌注(I/R)损伤是急性肾损伤(AKI)发生发展的一个重要因素,尤其在肾移植、心脏手术和严重低血压等临床情况下。自噬是一个清除受损细胞成分的关键过程,已被证明可通过减少氧化应激和提高细胞存活率来减轻I/R损伤。然而,当自噬被破坏时,它会加剧肾脏损伤。阐明自噬在I/R损伤中的作用对于揭示驱动AKI的分子机制至关重要,并且可能有助于基于自噬的治疗方法的开发。通过蛋白质印迹法、免疫组织化学(IHC)和免疫荧光(IF)染色技术分析蛋白质表达水平。使用染色质免疫沉淀(ChIP)、序列ChIP(ChIP-reChIP)和免疫共沉淀(Co-IP)试验探索沉默调节蛋白4(SIRT4)、SET结构域双叉组蛋白赖氨酸甲基转移酶1(SETDB1)和染色体盒蛋白同源物3(CBX3)之间的相互作用。还通过Co-IP检测SIRT4与第10号染色体同源丢失性磷酸酶-张力蛋白(PTEN)之间的关联。采用透射电子显微镜(TEM)观察自噬体。此外,建立了I/R损伤的体内大鼠模型以验证研究结果。在I/R损伤期间,Sirtuin 4(SIRT4)表达降低,自噬受损。此外,SIRT4与PTEN相互作用以调节其表达。此外,SETDB1介导组蛋白H3赖氨酸9三甲基化(H3K9me3)修饰,并将CBX3募集到SIRT4启动子,导致肾近端小管细胞中SIRT4表达受到抑制。重要的是,敲低SETDB1可上调SIRT4,降低PTEN表达,促进自噬,并在体内保护大鼠免受I/R损伤。SETDB1募集CBX3以调节SIRT4/PTEN轴,抑制自噬并促进I/R诱导的肾损伤。这些结果表明,靶向SETDB1-SIRT4轴可能提供一种减轻I/R诱导的AKI中肾损伤的新治疗策略。