4.5 Article

Protein kinase D mediates mitochondrion-to-nucleus signaling and detoxification from mitochondrial reactive oxygen species

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 25, Issue 19, Pages 8520-8530

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.25.19.8520-8530.2005

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Funding

  1. NCI NIH HHS [CA075134, R01 CA075134] Funding Source: Medline

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Efficient elimination of mitochondrial reactive oxygen species (mROS) correlates with increased cellular survival and organism life span. Detoxification of mitochondrial ROS is regulated by induction of the nuclear SOD2 gene, which encodes the manganese-dependent superoxide dismutase (MnSOD). However, the mechanisms by which mitochondrial oxidative stress activates cellular signaling pathways leading to induction of nuclear genes are not known. Here we demonstrate that release of mROS activates a signal relay pathway in which the serine/threonine protein kinase D (PKD) activates the NF-kappa B transcription factor, leading to induction of SOD2. Conversely, the FOX03a transcription factor is dispensable for mROS-induced SOD2 induction. PKD-mediated MnSOD expression promotes increased survival of cells upon release of mROS, suggesting that mitochondrion-to-nucleus signaling is necessary for efficient detoxification mechanisms and cellular viability.

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