SNORD3A Regulates STING Transcription to Promote Ferroptosis in Acute Kidney Injury

Abstract: Acute kidney injury (AKI) signifies a sudden and prolonged decline in kidney function characterized by tubular cell death and interstitial inflammation. Small nucleolar RNAs (snoRNAs) play pivotal roles in oxidative stress and inflammation, and may play an important role in the AKI process, which remains elusive. an elevated expression of Snord3a is revealed in renal tubules in response to AKI and demonstrates that Snord3a deficiency alleviates renal injury in AKI mouse models. Notably, the deficiency of Snord3a exhibits a mitigating effect on the stimulator of interferon genes (STING)‐associated ferroptosis phenotypes and the progression of tubular injury. Mechanistically, Snord3a is shown to regulate the STING signaling axis via promoting STING gene transcription; administration of Snord3a antisense oligonucleotides establishes a significant therapeutic advantage in AKI mouse models. Together, the findings elucidate the transcription regulation mechanism of STING and the crucial roles of the Snord3a‐STING axis in ferroptosis during AKI, underscoring Snord3a as a potential prognostic and therapeutic target for AKI.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
SNORD3A Regulates STING Transcription to Promote Ferroptosis in Acute Kidney Injury ; day:04 ; month:07 ; year:2024 ; extent:15
Advanced science ; (04.07.2024) (gesamt 15)

Creator
Zhu, Huanhuan
Wang, Junni
Miao, Jin
Shen, Mingdi
Wang, Huijing
Huang, Xiaohan
Ni, Anqi
Wu, Huijuan
Chen, Jianghua
Xiao, Liang
Xie, Shanshan
Lin, Weiqiang
Han, Fei

DOI
10.1002/advs.202400305
URN
urn:nbn:de:101:1-2407081429461.495551241506
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:49 AM CEST

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Associated

  • Zhu, Huanhuan
  • Wang, Junni
  • Miao, Jin
  • Shen, Mingdi
  • Wang, Huijing
  • Huang, Xiaohan
  • Ni, Anqi
  • Wu, Huijuan
  • Chen, Jianghua
  • Xiao, Liang
  • Xie, Shanshan
  • Lin, Weiqiang
  • Han, Fei

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