The radical-binding lipocalin A1M binds to a Complex I subunit and protects mitochondrial structure and function.

Magnus Gram, Lena Wester Rosenlöf, Heike Kotarsky, Tor Olofsson, Tomas Leanderson, Matthias Mörgelin, Vineta Fellman, Bo Åkerström

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Aims: During cell death, energy-consuming cell degradation and recycling programs are performed. Maintenance of energy-delivery during cell death is therefore crucial but the mechanisms to keep the mitochondrial functions intact during these processes are poorly understood. We have investigated the hypothesis that the heme- and radical-binding ubiquitous protein A1M (α<sub>1</sub>-microglobulin) is involved in protection of the mitochondria against oxidative insult during cell death. Results: Using blood cells, keratinocytes and liver cells, we show that A1M binds with high affinity to apoptosis-induced cells and is localized to mitochondria. The mitochondrial Complex I subunit NDUFAB1 was identified as a major molecular target of the A1M-binding. Furthermore, A1M was shown to inhibit the swelling of mitochondria, and to reverse the severely abrogated ATP-production of mitochondria when exposed to heme and ROS. Innovation: Import of the radical- and heme-binding protein A1M from the extracellular compartment confers protection of mitochondrial structure and function during cellular insult. Conclusion: A1M binds to a subunit of Complex I and has a role in assisting the mitochondria to maintain its energy delivery during cell death. A1M may also, at the same time, counteract and eliminate the ROS generated by the mitochondrial respiration to prevent oxidative damage to surrounding healthy tissue.
Original languageEnglish
Pages (from-to)2017-2028
JournalAntioxidants & Redox Signaling
Issue number16
Publication statusPublished - 2013

Subject classification (UKÄ)

  • Cell and Molecular Biology


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