Rhythmic oscillations of the microRNA miR-96-5p play a neuroprotective role by indirectly regulating glutathione levels

被引:67
|
作者
Kinoshita, Chisato [1 ]
Aoyama, Koji [1 ]
Matsumura, Nobuko [1 ]
Kikuchi-Utsumi, Kazue [1 ]
Watabe, Masahiko [1 ,2 ]
Nakaki, Toshio [1 ]
机构
[1] Teikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, Japan
[2] Teikyo Univ, Sch Med, Gen Med Educ Ctr, Itabashi Ku, Tokyo 1738605, Japan
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
关键词
OXIDATIVE STRESS; NEURONAL GLUTATHIONE; PARKINSONS-DISEASE; CIRCADIAN CLOCK; NEURODEGENERATIVE DISORDERS; KAIC PHOSPHORYLATION; LIPID-PEROXIDATION; MICE; DEFICIENCY; GLUTAMATE;
D O I
10.1038/ncomms4823
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glutathione (GSH) is a key antioxidant that plays an important neuroprotective role in the brain. Decreased GSH levels are associated with neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. Here we show that a diurnal fluctuation of GSH levels is correlated with neuroprotective activity against oxidative stress in dopaminergic cells. In addition, we found that the cysteine transporter excitatory amino acid carrier 1 (EAAC1), which is involved in neuronal GSH synthesis, is negatively regulated by the microRNA miR-96-5p, which exhibits a diurnal rhythm. Blocking miR-96-5p by intracerebroventricular administration of an inhibitor increased the level of EAAC1 as well as that of GSH and had a neuroprotective effect against oxidative stress in the mouse substantia nigra. Our results suggest that the diurnal rhythm of miR-96-5p may play a role in neuroprotection by regulating neuronal GSH levels via EAAC1.
引用
收藏
页数:10
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