Ferroptosis in microglial activation: a systematic review and multidata comparison

Ida Pesämaa1, Srinivas Koutarapu2, Henrik Zetterberg1,3,4,5,6,7

  • 1Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Gothenberg 413 45, Sweden.

Brain Communications
|April 10, 2026
PubMed

Insights

Ferroptosis, a cell death process involving lipid peroxidation, is explored in brain immune cells. This study identifies ferroptosis-related proteins and potential biomarkers for microglial activation.

Area of Science:

  • Neuroscience
  • Immunology
  • Cell Biology

Background:

  • Ferroptosis is a regulated cell death pathway characterized by iron dependence and lipid peroxidation.
  • This process has proinflammatory effects, suggesting a role in immune responses.
  • Microglia, the brain's innate immune cells, are understudied regarding ferroptosis and lipid peroxidation.

Purpose of the Study:

  • To review the concept of ferroptosis and its relevance to microglia.
  • To compile an extensive list of ferroptosis-related proteins.
  • To investigate ferroptosis in the context of microglial activation and identify potential biomarkers.

Main Methods:

  • Literature review and manual compilation of ferroptosis-relevant proteins.
  • Comparison of compiled protein lists with microglial activation signatures.
  • Analysis of ferroptosis-related changes in microglial activation models.

Main Results:

  • A comprehensive list of 120 ferroptosis-relevant proteins was generated, significantly expanding existing databases.
  • Ferroptosis-related changes were identified in models of microglial activation.
  • Several ferroptosis-relevant proteins were highlighted as potential biomarkers for ferroptosis in microglia.

Conclusions:

  • Ferroptosis is implicated in microglial activation and brain inflammation.
  • The identified proteins offer new insights into ferroptosis mechanisms in microglia.
  • Selected proteins show promise as biomarkers for ferroptosis and microglial dysfunction.

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