ISSN 1006-298X      CN 32-1425/R

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肾脏病与透析肾移植杂志 ›› 2026, Vol. 35 ›› Issue (5): 458-463.DOI: 10.3969/j.issn.1006-298X.2026.05.012

• 肾脏病基础 • 上一篇    下一篇

肾小管铁死亡重塑肾脏免疫微环境的研究进展

  

  • 出版日期:2026-10-27 发布日期:2026-10-27

Advances on renal tubular ferroptosis in remodeling the renal immune microenvironment

  • Online:2026-10-27 Published:2026-10-27

摘要:

铁死亡不仅导致肾小管上皮细胞丢失,还可将脂质过氧化事件转化为免疫信号。高糖、缺血/再灌注、感染性炎症和持续氧化应激可诱发肾小管铁死亡应激,促使其释放损伤相关分子模式、氧化脂质和细胞外囊泡,激活巨噬细胞、树突状细胞等,推动炎症放大、不良修复和慢性重塑。本文综述肾小管铁死亡的致病背景、信号释放、免疫感知和疾病转归,并评估干预措施和标志物价值。

关键词:

肾小管,铁死亡,免疫微环境,损伤相关分子模式,细胞外囊泡,急性肾损伤向慢性肾脏病转化

Abstract:

Ferroptosis of renal tubular epithelial cells not only leads to epithelial cell loss, but also converts lipid peroxidation events into immune signals. Hyperglycemia, ischemia-reperfusion, infectious inflammation and sustained oxidative stress promote ferroptotic stress and the release of damage-associated molecular patterns, oxidized lipids and extracellular vesicles. These signals activate macrophages and dendritic cells, amplifying inflammation, maladaptive repair and chronic remodeling. This review synthesizes the pathological contexts, signal-release mechanisms, immune sensing and disease outcomes of tubular ferroptosis. We also evaluate the value of related interventions and biomarkers.

Key words:

renal tubule, ferroptosis, immune microenvironment, damage-associated molecular pattern, extracellular vesicle, acute kidney injury to chronic kidney disease transition

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