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Updated: Jun 16, 2026

A Thermoplasmonic Approach for Investigating Plasma Membrane Repair in Living Cells and Model Membranes
Published on: January 19, 2024
Plasma membrane signaling induced by ionizing radiation
Isabelle Corre1, Colin Niaudet, Francois Paris
1Inserm UMR U892, Centre de Recherche en Cancérologie Nantes-Angers, Institut de Recherche Thérapeutique, 8 Quai Moncousu, F-44007 Nantes cedex 1, France.
Abstract:
For decades, DNA has been considered as the main cellular target of deleterious effects of ionizing radiation (IR). Nevertheless, molecular signals initiated at cellular membranes are now identified as critical events in a large spectrum of radiation-induced cellular processes. If IR provokes DNA damage directly by energy deposit on the DNA double helix and indirectly by reactive species, origin of IR-induced molecular events initiated at the plasma membrane remains more obscure. Generation of reactive oxygen/nitrogen species (ROS/RNS) inducing proteins and lipids modifications seems to be the prevalent hypothesis. However, spatial and temporal relocalization of proteins and/or lipids represents also potential mechanisms of cell signaling generation. In the context of an oxidative stress such as IR, the best example is the translocation of the enzyme acid sphingomyelinase (ASMase) from lysosomes to the outer layer of cell membrane, which then induces sphingomyelin hydrolysis and ceramide formation. Ceramide coalescence with cholesterol forms lipids microdomains in the plasma membrane, enhancing clustering of signaling receptors (death receptors like FAS, TNF, CD40, TRAIL or G protein-coupled receptors). In this manuscript, we propose to overview the different key molecular mechanisms induced at the plasma membrane after IR in perspective with their linked molecular actors.
Insights
Ionizing radiation (IR) triggers cell signaling at the plasma membrane, not just DNA damage. Acid sphingomyelinase (ASMase) translocation and ceramide formation are key radiation-induced membrane events.
Area of Science:
- Cellular Biology
- Radiation Biology
- Molecular Signaling
Background:
- Ionizing radiation (IR) traditionally targets DNA, but membrane-initiated signals are crucial for cellular responses.
- The precise mechanisms of IR-induced plasma membrane events are less understood than direct DNA damage.
- Reactive oxygen/nitrogen species (ROS/RNS) and protein/lipid relocalization are proposed signaling pathways.
Purpose of the Study:
- To review key molecular mechanisms at the plasma membrane following IR exposure.
- To highlight the molecular actors involved in radiation-induced membrane signaling.
- To provide a perspective on non-DNA-centric radiation effects.
Main Methods:
- Literature review of molecular mechanisms.
- Analysis of protein and lipid dynamics post-IR.
- Focus on sphingomyelinase (ASMase) pathway and ceramide generation.
Main Results:
- IR induces molecular events at the plasma membrane, including ROS/RNS generation and lipid/protein relocalization.
- Translocation of acid sphingomyelinase (ASMase) to the cell membrane triggers sphingomyelin hydrolysis and ceramide formation.
- Ceramide accumulation promotes lipid microdomain formation and clustering of signaling receptors.
Conclusions:
- Plasma membrane events are critical in the cellular response to IR.
- ASMase-mediated ceramide generation is a significant IR-induced signaling mechanism.
- Understanding membrane-initiated signaling offers new perspectives on IR effects.
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