4.8 Article

Engineering Ultrasmall Ferroptosis-Targeting and Reactive Oxygen/Nitrogen Species-Scavenging Nanozyme for Alleviating Acute Kidney Injury

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 32, 期 10, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202109221

关键词

acute kidney injuries; ferroptosis inhibition; KCa(H O-2)(2); [Fe (III)(CN) (6)]; H2O; nanozymes; multienzyme activities; reactive oxygen; nitrogen species scavenging

资金

  1. Basic Research Program of Shanghai Municipal Government [21JC1406002]
  2. Shanghai Science and Technology Program [21010500100]
  3. National Science Foundation for Young Scientists of China [51802336]
  4. National Nature Science Foundation of China [52072393, 81870517, 32070646]
  5. Youth Talent Program of Zhejiang Provincial Health Commission [2019RC313]
  6. Shanghai Association for Science and Technology Commission [19140905700]
  7. Shanghai Science and Technology Committee Rising-Star Program [21QA1403100]

向作者/读者索取更多资源

The study introduces a novel nanozyme CaPB, which mimics the activity of multiple enzymes, effectively clearing harmful substances and inhibiting renal damage, showing potential for treating kidney injury. Additionally, CaPB nanozymes significantly increase the expression of ferroptosis regulator and protect the kidney from oxidative injury, indicating a promising approach for AKI treatment.
Acute kidney injury (AKI) is a serious renal dysfunction syndromes, which predominantly correlates with the excess production of endogenous reactive oxygen/nitrogen species (RO/NSs), triggering a series of pathological processes including cellular apoptosis, renal fibrosis, and ferroptosis. Ferroptosis as an iron-dependent nonapoptotic regulated cell death is extensively involved in renal damage. Herein, the authors report the engineering of ultrasmall KCa(H2O)(2)[Fe-III(CN)(6)]center dot H2O nanoparticles as multienzyme mimetics, termed as CaPB nanozymes, for effectively scavenging RO/NSs and further inhibiting ferroptosis for the treatment of AKI. CaPB nanoparticles can effectively mimic the activity of multienzymes including superoxide dismutase, catalase, peroxidase, and glutathione peroxidase. Furthermore, CaPB nanozymes serving as a robust ferroptosis inhibitor significantly increase the expression of ferroptosis regulator glutathione peroxidase 4 in vitro. Furthermore, the renal accumulation of CaPB nanozymes effectively protects the kidney from oxidative injury and alleviated ferroptosis after intravenous administration. Additionally, the abnormal expression of inflammatory factors is further inhibited by CaPB nanozymes. The results demonstrate that the engineered ultrasmall CaPB nanozyme as a multienzyme mimetic features high potential for RO/NSs scavenging and treating AKI via inhibiting ferroptosis, which promises the clinical translation on the treatment of AKI and other RO/NSs-related renal diseases.

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