Entity

Time filter

Source Type

Stanford, CA, United States

Niizuma K.,Program in Neurosciences | Yoshioka H.,Program in Neurosciences | Chen H.,Program in Neurosciences | Kim G.S.,Program in Neurosciences | And 4 more authors.
Biochimica et Biophysica Acta - Molecular Basis of Disease | Year: 2010

Mitochondria play important roles as the powerhouse of the cell. After cerebral ischemia, mitochondria overproduce reactive oxygen species (ROS), which have been thoroughly studied with the use of superoxide dismutase transgenic or knockout animals. ROS directly damage lipids, proteins, and nucleic acids in the cell. Moreover, ROS activate various molecular signaling pathways. Apoptosis-related signals return to mitochondria, then mitochondria induce cell death through the release of pro-apoptotic proteins such as cytochrome c or apoptosis-inducing factor. Although the mechanisms of cell death after cerebral ischemia remain unclear, mitochondria obviously play a role by activating signaling pathways through ROS production and by regulating mitochondria-dependent apoptosis pathways. © 2009 Elsevier B.V. All rights reserved. Source

Discover hidden collaborations