The molecular activity of cells to their environment is
synchronized by the circadian clock. The "core clock" of the
circadian system is made up of a group of proteins that autonomously activate
and repress each other. BMAL1, one of the activating core clock proteins, is
critical for maintaining circadian rhythm and for controlling oxidative stress,
normal aging and cognitive ability.
In this issue of the Journal of
Clinical Investigation, Erik Musiek and colleagues at Washington University
School of Medicine asked whether BMAL1 and the rest of the core clock
contribute to the maintenance of healthy neurons. Using Bmal1-deficient
mice, the authors found that as these mice aged activated astrocytes began to
accumulate, a hallmark of active inflammation and damage. Bmal1-deficient
mice also displayed localized degeneration of neuronal cells and a loss of
functional connectivity, as measured by blood flow.
The researchers found that BMAL1 and the other activating core clock proteins
regulate important redox proteins that prevent damage caused by oxidative
stress. In an accompanying commentary, Colleen McClung from the University of
Pittsburgh noted that the activating circadian core clock proteins could be
explored as targets for future therapies for neurodegenerative diseases.
Source:Journal of Clinical Investigation,
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