The unusual suspect: A novel role for intermediate filament proteins in mitochondrial morphology
Mitochondrial dynamics is crucial for cellular homeostasis. However, not all proteins involved are known. Using a protein-protein interaction (PPI) approach, we identified ITPRIPL2 for involvement in mitochondrial dynamics. ITPRIPL2 co-localizes with intermediate filament protein vimentin, supported by protein simulations. ITPRIPL2 knockdown reveals mitochondrial elongation, disrupts vimentin processing, intermediate filament formation, and alters vimentin-related pathways. Interestingly, vimentin knockdown also leads to mitochondrial elongation. These findings highlight ITPRIPL2 as vimentin-associated protein essential for intermediate filament structure and suggest a role for intermediate filaments in mitochondrial morphology. Our study demonstrates that PPI analysis is a powerful approach for identifying novel mitochondrial dynamics proteins.
Authors
- Simon Denil (ORCID: https://orcid.org/0000-0001-7242-9082)
- Irene M. G. M. Hemel (ORCID: https://orcid.org/0000-0002-8841-7374)
- Mike Gerards (ORCID: https://orcid.org/0000-0003-4886-8055)
- Martina Kutmon
- Michiel Adriaens (ORCID: https://orcid.org/0000-0002-4472-7119)
- Gökhan Ertaylan (ORCID: https://orcid.org/0000-0001-5602-6435)
- Carlijn Steen
Institutions
- Maastricht University Medical Centre (NL)
- Maastricht University (NL)
- Flemish Institute for Technological Research (BE)
Publication Details
- Journal
- Mitochondrion
- Published
- 2025-02-03
- DOI
- https://doi.org/10.1016/j.mito.2025.102008
- Citations
- 4
- Primary Topic
- Mitochondrial Function and Pathology
- Type
- article
- Field-Weighted Citation Impact
- 3.22
Funders
- Universiteit Maastricht