Ji Ming-Lu, Wang Jia-Nan, Wu Ming-Fei, Xu Chuan-Hui, Zhang Meng-Meng, Chang Wen-Bao, Mao Xin-Fei, Li Chao, Yu Ju-Tao, Zhang Dan-Feng, Suo Xiao-Guo, Diao Shao-Xi, Ma Nan-Nan, Chen Ying, Hou Rui, Lu Hao, Xie Shuai-Shuai, Dong Yu-Hang, Zhu Qi, Chen Xin, Xu Tao, Shao Wei, Jin Juan, Wen Jia-Gen, Dong Xiao-Wu, Wang Wen-Bin, Che Jin-Xin, Meng Xiao-Ming
Inflammation and Immune-Mediated Diseases Laboratory of Anhui Province, The Key Laboratory of Anti-inflammatory of Immune Medicines, Ministry of Education, Anhui Institute of Innovative Drugs, School of Pharmacy, Anhui Medical University, Hefei, 230032, China.
Hangzhou Institute of Innovative Medicine, Institute of Drug Discovery and Design, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, 310058, China.
EBioMedicine. 2025 Jun;116:105739. doi: 10.1016/j.ebiom.2025.105739. Epub 2025 May 8.
Acute kidney injury (AKI) is a critical clinical syndrome with high morbidity, mortality, and no effective treatment in clinical practice. The role of the Signal Transducer and Activator of Transcription 3 (Stat3) in AKI remains controversial, and its complex regulatory mechanisms must be further explored.
We generated renal tubular epithelial cells Stat3 conditional knockout (cKO) mice and used them in cecal ligation and puncture (CLP) and ischaemia-reperfusion (I/R) induced AKI models. Additionally, proteolysis-targeting chimaera (PROTAC) compound E034 was designed and synthesised. We also utilised human kidney tissues, mouse renal tubular epithelial cells (mTECs) and HK-2 cells for further studies, including immunohistochemistry, Western blot analysis, Real-time PCR, chromatin immunoprecipitation (ChIP) and RNA sequencing, scanning electron microscopy (SEM) and Co-Immunoprecipitation (Co-IP) assay.
An upregulation of total Stat3 protein was observed in AKI mouse models, which correlated with patient biopsy results. This increase may be attributed to histone H3K27 acetylation. Stat3 knockout in renal tubular epithelial cells significantly reduced AKI injury and inflammation in mice. Mechanistically, Stat3 induces the transcription of tripartite motif-containing protein 21 (Trim21), triggering a cascade that activates gasdermin D (Gsdmd), resulting in pyroptosis. Administration of E034, which selectively targets Stat3 for ubiquitination and degradation, significantly alleviated renal injury in a low-dose, single-dose regimen.
In the context of renal injury, PROTAC emerges as a promising modality by explicitly targeting the Stat3/Trim21/Gsdmd axis, which our study has identified as a potential therapeutic target, potentially endowing clinically significant therapeutic strategies.
This work was supported by the National Key R&D Program (2022YFC2502503), the National Natural Science Foundation of China (No. 82270738), the National Natural Science Foundation of China (No. 82400806) and the Graduate Research and Practice Innovation Project of Anhui Medical University (YJS20230059).
急性肾损伤(AKI)是一种严重的临床综合征,发病率和死亡率高,且临床实践中尚无有效治疗方法。信号转导和转录激活因子3(Stat3)在急性肾损伤中的作用仍存在争议,其复杂的调控机制有待进一步探索。
我们构建了肾小管上皮细胞Stat3条件性敲除(cKO)小鼠,并将其用于盲肠结扎和穿刺(CLP)及缺血再灌注(I/R)诱导的急性肾损伤模型。此外,设计并合成了靶向蛋白水解嵌合体(PROTAC)化合物E034。我们还利用人肾组织、小鼠肾小管上皮细胞(mTECs)和HK-2细胞进行进一步研究,包括免疫组织化学、蛋白质印迹分析、实时定量PCR、染色质免疫沉淀(ChIP)和RNA测序、扫描电子显微镜(SEM)和免疫共沉淀(Co-IP)分析。
在急性肾损伤小鼠模型中观察到总Stat3蛋白上调,这与患者活检结果相关。这种增加可能归因于组蛋白H3K27乙酰化。肾小管上皮细胞中Stat3基因敲除显著减轻了小鼠的急性肾损伤和炎症。机制上,Stat3诱导含三联基序蛋白21(Trim21)的转录,引发激活gasdermin D(Gsdmd)的级联反应,导致细胞焦亡。给予E034,其选择性靶向Stat3进行泛素化和降解,在低剂量单剂量方案中显著减轻了肾损伤。
在肾损伤的背景下,PROTAC通过明确靶向Stat3/Trim21/Gsdmd轴成为一种有前景的治疗方式,我们已将该轴确定为潜在治疗靶点,这可能为临床带来具有重要意义的治疗策略。
本研究得到国家重点研发计划(2022YFC2502503)、国家自然科学基金(82270738)、国家自然科学基金(编号82400806)以及安徽医科大学研究生科研与实践创新项目(YJS20230059)的支持。