PXD059070 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Mitochondrial stress drives skeletal muscle remodelling following sprint-interval exercise. |
| Description | Mitochondria play a central role in cellular metabolism and are crucial for maintaining cellular health. Exercise is a proven intervention to enhance mitochondrial function and prevent non-communicable diseases, yet the molecular mechanisms driving exercise-induced mitochondrial remodelling remain unclear. This study compares the effects of moderate-intensity continuous exercise (MICE) and sprint-interval exercise (SIE) on mitochondrial adaptations. We demonstrate that SIE induces mitochondrial stress and activates the mitochondrial unfolded protein response (UPRmt), alongside disturbances in mitochondrial structure while MICE promotes mitochondrial adaptations characterized by increased mitochondrial content. Over an 8-week training period, moderate-intensity continuous training (MICT) and sprint-interval training (SIT) show divergent mitochondrial remodelling. Findings provide novel insights into the mechanisms by which different exercise prescriptions modulate mitochondrial signalling and remodelling in human skeletal muscle, offering a basis for personalized exercise strategies to optimize mitochondrial health. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-01-12 |
| AnnouncementXML | Submission_2026-01-11_18:54:13.861.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | David Stroud |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | acetylated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Eclipse |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2024-12-19 22:19:37 | ID requested | |
| ⏵ 1 | 2026-01-11 18:54:14 | announced | |
Publication List
| 10.1038/s41467-025-66625-8; |
| Botella J, Perri E, Caruana NJ, L, ó, pez-Calcerrada S, Brischigliaro M, Jamnick NA, Oorschot V, Saner NJ, D, í, az-Lara J, Taylor DF, Garnham A, Fern, á, ndez-Vizarra E, Ugalde C, Ramm G, Stroud DA, Lazarou M, Bishop DJ, Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in men. Nat Commun, 17(1):71(2025) [pubmed] |
Keyword List
| submitter keyword: Exercise,Mitochondria, Muscle, DIA, Human |
Contact List
| David Stroud |
| contact affiliation | Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, VIC, 3010, Australia 2Murdoch Children’s Research Institute, Melbourne, VIC 3052, Australia 3Victorian Clinical Genetics Services, Murdoch Children’s Research Institute, Melbourne, VIC, 3052, Australia |
| contact email | david.stroud@unimelb.edu.au |
| lab head | |
| David Stroud |
| contact affiliation | The University of Melbourne |
| contact email | david.stroud@unimelb.edu.au |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/01/PXD059070 |
| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD059070
- Label: PRIDE project
- Name: Mitochondrial stress drives skeletal muscle remodelling following sprint-interval exercise.