Research Project
Grant-in-Aid for Young Scientists (B)
An experimental assay system was employed to generate excessive ROS in the mitochondria in a precisely controlled spatio-temporal manner. Using mammalian cells and worm C. elegans generating mitochondrial ROS, I analyzed the stress response and the molecular mechanism induced by mitochondrial ROS in vitro and in vivo. I revealed that factors involved in the mitochondrial permeability transition (Cyclophilin D and Ca++) were contributed to the mitochondrial oxidative stress response.
All 2010 Other
All Presentation (4 results) Remarks (1 results)
http://www.med.osaka-u.ac.jp/pub/gene/www/laboratory/shibuya1.html