Author
Listed:
- Jorge Gómez-Deza
(National Institutes of Health)
- Matthew Nebiyou
(National Institutes of Health)
- Mor R. Alkaslasi
(National Institutes of Health)
- Francisco M. Nadal-Nicolás
(National Institutes of Health)
- Preethi Somasundaram
(Baylor College of Medicine)
- Anastasia L. Slavutsky
(National Institutes of Health)
- Wei Li
(National Institutes of Health)
- Michael E. Ward
(National Institutes of Health)
- Trent A. Watkins
(Baylor College of Medicine
University of California at San Francisco)
- Claire E. Le Pichon
(National Institutes of Health)
Abstract
Currently there are no effective treatments for an array of neurodegenerative disorders to a large part because cell-based models fail to recapitulate disease. Here we develop a reproducible human iPSC-based model where laser axotomy causes retrograde axon degeneration leading to neuronal cell death. Time-lapse confocal imaging revealed that damage triggers an apoptotic wave of mitochondrial fission proceeding from the site of injury to the soma. We demonstrate that this apoptotic wave is locally initiated in the axon by dual leucine zipper kinase (DLK). We find that mitochondrial fission and resultant cell death are entirely dependent on phosphorylation of dynamin related protein 1 (DRP1) downstream of DLK, revealing a mechanism by which DLK can drive apoptosis. Importantly, we show that CRISPR mediated Drp1 depletion protects mouse retinal ganglion neurons from degeneration after optic nerve crush. Our results provide a platform for studying degeneration of human neurons, pinpoint key early events in damage related neural death and provide potential focus for therapeutic intervention.
Suggested Citation
Jorge Gómez-Deza & Matthew Nebiyou & Mor R. Alkaslasi & Francisco M. Nadal-Nicolás & Preethi Somasundaram & Anastasia L. Slavutsky & Wei Li & Michael E. Ward & Trent A. Watkins & Claire E. Le Pichon, 2024.
"DLK-dependent axonal mitochondrial fission drives degeneration after axotomy,"
Nature Communications, Nature, vol. 15(1), pages 1-18, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54982-9
DOI: 10.1038/s41467-024-54982-9
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54982-9. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.