Format

Send to

Choose Destination
Trends Cell Biol. 2007 Jan;17(1):13-8. Epub 2006 Nov 28.

Mitochondrial ROS--radical detoxification, mediated by protein kinase D.

Author information

1
Department of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Griffin Building, Room 306, 4500 San Pablo Road, Jacksonville, FL 32224, USA. storz.peter@mayo.edu <storz.peter@mayo.edu>

Abstract

The mitochondrial electron transport chain is the major source for the production of oxygen radicals. Mitochondria-generated reactive oxygen species (mROS) have been implicated in decreasing the life span and contributing to age-related diseases (known as the free radical theory of aging). Recently, the serine/threonine kinase protein kinase D1 (PKD1) was identified as a mitochondrial sensor for oxidative stress. mROS-activated PKD regulates a radical-sensing signaling pathway, which relays mROS production to the induction of nuclear genes that mediate cellular detoxification and survival. This PKD regulated signaling pathway is the first known mitochondria located and mitochondrially regulated antioxidant system that protects these organelles and cells from oxidative stress-mediated damage or cell death. The identification of this and further intracellular protective signaling pathways provides an opportunity to manipulate the effects of mROS, and might provide the key to targeting aging effects and age-related diseases that have been linked to mitochondrial dysfunctions.

PMID:
17126550
DOI:
10.1016/j.tcb.2006.11.003
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center