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Published on: January 22, 2019
Targeting Stat3 with conditional knockout or PROTAC technology alleviates renal injury by Limiting pyroptosis
Ming-Lu Ji1, Jia-Nan Wang1, Ming-Fei Wu2
1Inflammation 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.
Background:
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.
Methods:
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.
Findings:
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.
Interpretation:
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.
Funding:
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).
Insights
Targeting Signal Transducer and Activator of Transcription 3 (Stat3) with proteolysis-targeting chimaera (PROTAC) compound E034 effectively reduced acute kidney injury (AKI). This novel approach targets the Stat3/Trim21/Gsdmd pathway, offering a promising therapeutic strategy for renal injury.
Area of Science:
- Nephrology
- Molecular Biology
- Biochemistry
Background:
- Acute kidney injury (AKI) presents significant clinical challenges with high morbidity and mortality.
- The precise role and regulatory mechanisms of Signal Transducer and Activator of Transcription 3 (Stat3) in AKI are not fully understood.
Purpose of the Study:
- To investigate the role of Stat3 in renal tubular epithelial cells during AKI.
- To explore the therapeutic potential of targeting Stat3 in AKI using a novel proteolysis-targeting chimaera (PROTAC) compound.
Main Methods:
- Generated Stat3 conditional knockout (cKO) mice for AKI models (cecal ligation and puncture, ischemia-reperfusion).
- Designed and synthesized PROTAC compound E034 to target Stat3 for degradation.
- Utilized human kidney tissues, mouse renal tubular epithelial cells (mTECs), and HK-2 cells for molecular analyses (immunohistochemistry, Western blot, qPCR, ChIP, RNA sequencing, SEM, Co-IP).
Main Results:
- Upregulation of total Stat3 protein was observed in AKI models and human biopsies, potentially linked to histone H3K27 acetylation.
- Stat3 knockout in renal tubular epithelial cells significantly attenuated AKI-induced injury and inflammation.
- Stat3 was found to induce tripartite motif-containing protein 21 (Trim21) transcription, activating gasdermin D (Gsdmd) and leading to pyroptosis.
- PROTAC E034 administration effectively alleviated renal injury in AKI models.
Conclusions:
- The Stat3/Trim21/Gsdmd axis is identified as a key pathway in renal injury.
- PROTAC-mediated targeted degradation of Stat3 represents a promising therapeutic strategy for AKI.
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