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Título: | Deciphering peroxisomal reactive species interactome and redox signalling networks |
Autor: | Sandalio, Luisa M. CSIC ORCID ; Collado-Arenal, Aurelio M. CSIC; Romero-Puertas, María C. CSIC ORCID | Palabras clave: | Interactome Peroxisome Reactive nitrogen species Reactive oxygen species Reactive sufur species Reactive carbonyl species Redox signaling Retrograde signaling |
Fecha de publicación: | 2023 | Editor: | Elsevier | Citación: | Free Radical Biology and Medicine 197: 58-70 (2023) | Resumen: | Plant peroxisomes are highly dynamic organelles with regard to metabolic pathways, number and morphology and participate in different metabolic processes and cell responses to their environment. Peroxisomes from animal and plant cells house a complex system of reactive oxygen species (ROS) production associated to different metabolic pathways which are under control of an important set of enzymatic and non enzymatic antioxidative defenses. Nitric oxide (NO) and its derivate reactive nitrogen species (RNS) are also produced in these organelles. Peroxisomes can regulate ROS and NO/RNS levels to allow their role as signalling molecules. The metabolism of other reactive species such as carbonyl reactive species (CRS) and sulfur reactive species (SRS) in peroxisomes and their relationship with ROS and NO have not been explored in depth. In this review, we define a peroxisomal reactive species interactome (PRSI), including all reactive species ROS, RNS, CRS and SRS, their interaction and effect on target molecules contributing to the dynamic redox/ROS homeostasis and plasticity of peroxisomes, enabling fine-tuned regulation of signalling networks associated with peroxisome-dependent HO. Particular attention will be paid to update the information available on HO-dependent peroxisomal retrograde signalling and to discuss a specific peroxisomal footprint. | Versión del editor: | http://dx.doi.org/10.1016/j.freeradbiomed.2023.01.014 | URI: | http://hdl.handle.net/10261/335490 | DOI: | 10.1016/j.freeradbiomed.2023.01.014 | Identificadores: | doi: 10.1016/j.freeradbiomed.2023.01.014 issn: 1873-4596 |
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