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N-methyl-D-aspartate receptor regulates the circadian clock in megakaryocytic cells and impacts cell proliferation through BMAL1
N-methyl-D-aspartate receptor controls the daily rhythm in platelet-forming cells and affects their growth through BMAL1
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Abstract
Megakaryocytic cells exhibit disrupted circadian rhythms when N-methyl-D-aspartate receptor (NMDAR) is inhibited.
- Both the Meg-01 megakaryocytic cell line and native murine megakaryocytes express circadian clock genes.
- Deletion of the Grin1 gene in megakaryocytes resulted in significant disruption of circadian rhythm signaling and increased BMAL1 protein levels.
- Inhibition of NMDAR in Meg-01 cells led to widespread changes in the expression of clock genes, including increased BMAL1 levels.
- Overexpression of BMAL1 was associated with reduced cell proliferation and altered expression of cell cycle regulators MYC and WEE1.
- Knockdown of BMAL1 resulted in increased cell death in Meg-01 cells with inhibited NMDAR.
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