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.

Ebiomedicine
|May 9, 2025
PubMed
Abstract

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.