期刊
REDOX BIOLOGY
卷 37, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.redox.2020.101712
关键词
Drosophila; Glutathione; Hydrogen Peroxide; ROS
资金
- BBSRC [BB/I012273/1, BB/M002322/1]
- Wellcome Trust through the Centre for Future Health (CFH) at the University of York [204829]
- BBSRC [BB/I01179X/1, BB/M002322/1, BB/I012273/1] Funding Source: UKRI
Reactive oxygen species (ROS) are generated during physiological bouts of synaptic activity and as a consequence of pathological conditions in the central nervous system. How neurons respond to and distinguish between ROS in these different contexts is currently unknown. In Drosophila mutants with enhanced JNK activity, lower levels of ROS are observed and these animals are resistant to both changes in ROS and changes in synapse morphology induced by oxidative stress. In wild type flies, disrupting JNK-AP-1 signalling perturbs redox homeostasis suggesting JNK activity positively regulates neuronal antioxidant defense. We validated this hypothesis in mammalian neurons, finding that JNK activity regulates the expression of the antioxidant gene Srxn-1, in a c-Jun dependent manner. We describe a conserved 'adaptive' role for neuronal JNK in the maintenance of redox homeostasis that is relevant to several neurodegenerative diseases.
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