4.5 Article

Association of Omi/HtrA2 with γ-secretase in mitochondria

Journal

NEUROCHEMISTRY INTERNATIONAL
Volume 57, Issue 6, Pages 668-675

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2010.08.004

Keywords

Omi/HtrA2; Presenilin; gamma-Secretase; Mitochondria; AICD

Funding

  1. Foundation for Geriatric Diseases at Karolinska Institutet
  2. Gun and Bertil Stohnes's Foundation
  3. Loo and Hans Ostermans Foundation
  4. Swedish Brain Power Program
  5. Strategic Neuroscience Program
  6. Dainippon Sumitomo Pharma Company, Ltd.
  7. Knut and Alice Wallenbergs Foundation

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Omi/HtrA2, a mitochondrial serine protease with chaperone activity, is involved in varied intracellular processes. Dysfunctional Omi/HtrA2 has thus been implicated in various neurodegenerative disorders. Previously, we have shown that gamma-secretase complexes are present and active in mitochondria. Here, we demonstrate that peptide corresponding to C-terminus of presenilin-1, as previously reported to activate Omi/HtrA2, interacts with Omi/HtrA2 in isolated mitochondria. Moreover, we show that Omi/HtrA2 interacts with presenilin in active gamma-secretase complexes located to mitochondria. Using a biotinylated gamma-secretase inhibitor and confocal microscopy, we could further confirm the association of gamma-secretase complexes with mitochondrial Omi/HtrA2. Furthermore, determination of gamma-secretase complex topology in isolated mitochondria revealed an association of gamma-secretase complexes with the outer membrane of mitochondria with the extreme PSI C-terminus facing the inter-membrane space. We have also studied the impact of Omi/HtrA2 on gamma-secretase activity, measuring APP intracellular domain (AICD) production. We found reduced AICD production in mitochondria isolated from Omi/HtrA2 knockout mouse embryonic fibroblasts, indicating a significant role of Omi/HtrA2 on gamma-secretase activity. Thus, our results provide information for understanding the interplay between mitochondria! Omi/HtrA2 and gamma-secretase complexes in AD. (c) 2010 Elsevier Ltd. All rights reserved.

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