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Redox-Mediated Rewiring of Signalling Pathways: The Role of a Cellular Clock in Brain Health and Disease

Journal

ANTIOXIDANTS
Volume 12, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/antiox12101873

Keywords

brain development; neurodegenerative disorders; redox; mitochondria; cellular clock

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This article reviews the network topology of key signaling pathways, with a focus on redox-sensitive proteins such as PTEN and Ras GTPase, which have the ability to reshape the connectivity profile of signaling pathways based on altered redox states. It proposes that redox-mediated rewiring is essential for regulating the rate of transmission of biological signals and suggests the existence of a programmable cellular clock that orchestrates the pace of biological phenomena. Furthermore, it discusses the evidence that abnormal redox-mediated modulation of the cellular clock output contributes to pathological conditions affecting the human brain.
Metazoan signalling pathways can be rewired to dampen or amplify the rate of events, such as those that occur in development and aging. Given that a linear network topology restricts the capacity to rewire signalling pathways, such scalability of the pace of biological events suggests the existence of programmable non-linear elements in the underlying signalling pathways. Here, we review the network topology of key signalling pathways with a focus on redox-sensitive proteins, including PTEN and Ras GTPase, that reshape the connectivity profile of signalling pathways in response to an altered redox state. While this network-level impact of redox is achieved by the modulation of individual redox-sensitive proteins, it is the population by these proteins of critical nodes in a network topology of signal transduction pathways that amplifies the impact of redox-mediated reprogramming. We propose that redox-mediated rewiring is essential to regulate the rate of transmission of biological signals, giving rise to a programmable cellular clock that orchestrates the pace of biological phenomena such as development and aging. We further review the evidence that an aberrant redox-mediated modulation of output of the cellular clock contributes to the emergence of pathological conditions affecting the human brain.

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