Rhythmic oscillations of the microRNA miR-96-5p play a neuroprotective role by indirectly regulating glutathione levels
被引:69
作者:
Kinoshita, Chisato
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Teikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, JapanTeikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, Japan
Kinoshita, Chisato
[1
]
Aoyama, Koji
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Teikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, JapanTeikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, Japan
Aoyama, Koji
[1
]
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Matsumura, Nobuko
[1
]
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Kikuchi-Utsumi, Kazue
[1
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Watabe, Masahiko
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Teikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, Japan
Teikyo Univ, Sch Med, Gen Med Educ Ctr, Itabashi Ku, Tokyo 1738605, JapanTeikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, Japan
Watabe, Masahiko
[1
,2
]
Nakaki, Toshio
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Teikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, JapanTeikyo Univ, Sch Med, Dept Pharmacol, Itabashi Ku, Tokyo 1738605, Japan
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
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.
机构:
MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
MIT, Dept Biol, Cambridge, MA 02139 USA
Whitehead Inst Biomed Res, Cambridge, MA 02142 USAMIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
机构:
MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
MIT, Dept Biol, Cambridge, MA 02139 USA
Whitehead Inst Biomed Res, Cambridge, MA 02142 USAMIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA