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Updated: May 3, 2026

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Published on: November 18, 2014
IRAS is an anti-apoptotic protein
Monique Dontenwill1, John E Piletz, Michael Chen
1Pharmacologie et Physicochimie des Interactions Cellulaires et Moléculaires, UMR CNRS 7034, Faculté de Pharmacie, Université Louis Pasteur de Strasbourg, Illkirch, France. mdontenwill@aspirine.u-strasbg.fr
Researchers discovered that IRAS, a protein previously known for binding imidazoline ligands, functions to prevent active cell death (apoptosis). This finding offers new insights into regulating cell survival and disease pathways.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Active cell death (apoptosis) plays a role in diseases like cancer and neurodegenerative disorders.
- IRAS protein was previously identified to bind imidazoline ligands.
- Human IRAS (hIRAS) shares homology with rat IRAS and mouse nischarin, which binds alpha5 integrin.
Purpose of the Study:
- To investigate the function of IRAS, specifically its role in apoptosis.
- To characterize the anti-apoptotic properties of human IRAS (hIRAS).
Main Methods:
- Stable transfection of hIRAS into PC12 cells and transient transfection into COS7 cells.
- Assessment of cell survival under apoptotic stimuli (serum starvation, thapsigargin, staurosporine).
- Measurement of caspase-3 activity, phosphatidylserine translocation, and nuclear fragmentation.
Main Results:
- hIRAS expression in PC12 cells prolonged survival against apoptotic stimuli.
- The apoptotic population was reduced in hIRAS-expressing cells.
- Protection involved decreased caspase-3 activity, phosphatidylserine translocation, and nuclear fragmentation, with possible PI3 kinase pathway involvement.
Conclusions:
- IRAS exhibits a previously unrecognized anti-apoptotic function.
- IRAS is involved in the regulation of cell survival.
- IRAS represents a novel target for understanding and potentially treating diseases involving apoptosis.
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