Cargando…
The Redox architecture of physiological function
The ability of organisms to accommodate variations in metabolic need and environmental conditions is essential for their survival. However, an explanation is lacking as to how the necessary accommodations in response to these challenges are organized and coordinated from (sub)cellular to higher-leve...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686734/ https://www.ncbi.nlm.nih.gov/pubmed/31417975 http://dx.doi.org/10.1016/j.cophys.2019.04.009 |
_version_ | 1783442623865815040 |
---|---|
author | Santolini, Jerome Wootton, Stephen A Jackson, Alan A Feelisch, Martin |
author_facet | Santolini, Jerome Wootton, Stephen A Jackson, Alan A Feelisch, Martin |
author_sort | Santolini, Jerome |
collection | PubMed |
description | The ability of organisms to accommodate variations in metabolic need and environmental conditions is essential for their survival. However, an explanation is lacking as to how the necessary accommodations in response to these challenges are organized and coordinated from (sub)cellular to higher-level physiological functions, especially in mammals. We propose that the chemistry that enables coordination and synchronization of these processes dates to the origins of Life. We offer a conceptual framework based upon the nature of electron exchange (Redox) processes that co-evolved with biological complexification, giving rise to a multi-layered system in which intra/intercellular and inter-organ exchange processes essential to sensing and adaptation stay fully synchronized. Our analysis explains why Redox is both the lingua franca and the mechanism that enable integration by connecting the various elements of regulatory processes. We here define these interactions across levels of organization as the ‘Redox Interactome’. This framework provides novel insight into the chemical and biological basis of Redox signalling and may explain the recent convergence of metabolism, bioenergetics, and inflammation as well as the relationship between Redox stress and human disease. |
format | Online Article Text |
id | pubmed-6686734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-66867342019-08-13 The Redox architecture of physiological function Santolini, Jerome Wootton, Stephen A Jackson, Alan A Feelisch, Martin Curr Opin Physiol Article The ability of organisms to accommodate variations in metabolic need and environmental conditions is essential for their survival. However, an explanation is lacking as to how the necessary accommodations in response to these challenges are organized and coordinated from (sub)cellular to higher-level physiological functions, especially in mammals. We propose that the chemistry that enables coordination and synchronization of these processes dates to the origins of Life. We offer a conceptual framework based upon the nature of electron exchange (Redox) processes that co-evolved with biological complexification, giving rise to a multi-layered system in which intra/intercellular and inter-organ exchange processes essential to sensing and adaptation stay fully synchronized. Our analysis explains why Redox is both the lingua franca and the mechanism that enable integration by connecting the various elements of regulatory processes. We here define these interactions across levels of organization as the ‘Redox Interactome’. This framework provides novel insight into the chemical and biological basis of Redox signalling and may explain the recent convergence of metabolism, bioenergetics, and inflammation as well as the relationship between Redox stress and human disease. Elsevier Ltd 2019-06 /pmc/articles/PMC6686734/ /pubmed/31417975 http://dx.doi.org/10.1016/j.cophys.2019.04.009 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Santolini, Jerome Wootton, Stephen A Jackson, Alan A Feelisch, Martin The Redox architecture of physiological function |
title | The Redox architecture of physiological function |
title_full | The Redox architecture of physiological function |
title_fullStr | The Redox architecture of physiological function |
title_full_unstemmed | The Redox architecture of physiological function |
title_short | The Redox architecture of physiological function |
title_sort | redox architecture of physiological function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686734/ https://www.ncbi.nlm.nih.gov/pubmed/31417975 http://dx.doi.org/10.1016/j.cophys.2019.04.009 |
work_keys_str_mv | AT santolinijerome theredoxarchitectureofphysiologicalfunction AT woottonstephena theredoxarchitectureofphysiologicalfunction AT jacksonalana theredoxarchitectureofphysiologicalfunction AT feelischmartin theredoxarchitectureofphysiologicalfunction AT santolinijerome redoxarchitectureofphysiologicalfunction AT woottonstephena redoxarchitectureofphysiologicalfunction AT jacksonalana redoxarchitectureofphysiologicalfunction AT feelischmartin redoxarchitectureofphysiologicalfunction |