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.

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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

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article

The unusual suspect: A novel role for intermediate filament proteins in mitochondrial morphology

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Mitochondrial Function and Pathology
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article

The unusual suspect: A novel role for intermediate filament proteins in mitochondrial morphology

Simon Denil, Irene M. G. M. Hemel, Mike Gerards, Martina Kutmon, Michiel Adriaens, Gökhan Ertaylan, Carlijn Steen
article en
4 citations

Abstract

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.

MitochondrionVol. 81
Maastricht University Medical Centre (NL), Maastricht University (NL), Flemish Institute for Technological Research (BE)
Universiteit Maastricht
Zero hunger
Openalex Percentile: Top 9%
Mitochondrial Function and Pathology
3.22
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