Rockenfeller, Patrick, Smolnig, Martin, Diessl, Jutta, Bashir, Mina, Schmiedhofer, Vera, Knittelfelder, Oskar, Ring, Julia, Franz, Joakim, Foessl, Ines, Khan, Muhammad J., and others. (2018) Diacylglycerol triggers Rim101 pathway dependent necrosis in yeast: a model for lipotoxicity. Cell Death and Differentiation, 25 . pp. 767-783. ISSN 1350-9047. E-ISSN 1476-5403. (doi:10.1038/s41418-017-0014-2) (KAR id:64728)
PDF
Publisher pdf
Language: English
This work is licensed under a Creative Commons Attribution 4.0 International License.
|
|
Download this file (PDF/4MB) |
Preview |
Request a format suitable for use with assistive technology e.g. a screenreader | |
PDF
Author's Accepted Manuscript
Language: English Restricted to Repository staff only |
|
Contact us about this Publication
|
|
Official URL: http://dx.doi.org/10.1038/s41418-017-0014-2 |
Abstract
The loss of lipid homeostasis can lead to lipid overload and is associated with a variety of disease states. However, little is known as to how the disruption of lipid regulation or lipid overload affects cell survival. In this study we investigated how excess diacylglycerol (DG), a cardinal metabolite suspected to mediate lipotoxicity, compromises the survival of yeast cells. We reveal that increased DG achieved by either genetic manipulation or pharmacological administration of 1,2-dioctanoyl-sn-glycerol (DOG) triggers necrotic cell death. The toxic effects of DG are linked to glucose metabolism and require a functional Rim101 signaling cascade involving the Rim21 dependent sensing complex and activation of a calpain-like protease. The Rim101 cascade is an established pathway that triggers a transcriptional response to alkaline or lipid stress. We propose that the Rim101 pathway senses DG-induced lipid perturbation and conducts a signaling response that either facilitates cellular adaptation or triggers lipotoxic cell death. Using established models of lipotoxicity i.e. high fat diet in Drosophila and palmitic acid administration in cultured human endothelial cells, we present evidence that the core mechanism underlying this calpain-dependent lipotoxic cell death pathway is phylogenetically conserved.
Item Type: | Article |
---|---|
DOI/Identification number: | 10.1038/s41418-017-0014-2 |
Uncontrolled keywords: | Diacylglycerol, calpain, cell death, glucose-repression, hexokinase, lipotoxicity, necrosis, Rim13, Rim101 |
Divisions: | Divisions > Division of Natural Sciences > Biosciences |
Depositing User: | Campbell Gourlay |
Date Deposited: | 24 Nov 2017 15:34 UTC |
Last Modified: | 05 Nov 2024 11:01 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/64728 (The current URI for this page, for reference purposes) |
- Link to SensusAccess
- Export to:
- RefWorks
- EPrints3 XML
- BibTeX
- CSV
- Depositors only (login required):