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Glutathione transferase Omega 1-1 (GSTO1-1) modulates Akt and MEK1/2 signaling in human neuroblastoma cell SH-SY5Y
被引:11
|作者:
Saisawang, Chonticha
[1
]
Wongsantichon, Jantana
[2
,3
]
Robinson, Robert C.
[2
,4
]
Ketternnan, Albert J.
[1
]
机构:
[1] Mahidol Univ, Inst Mol Biosci, Salaya Campus,25-25 Putthamonthol Rd 4, Salaya 73170, Nakhon Pathom, Thailand
[2] ASTAR, Inst Mol & Cell Biol, Singapore, Singapore
[3] Mahidol Oxford Trop Med Res Unit MORU, Bangkok, Thailand
[4] Okayama Univ, Res Inst Interdisciplinary Sci, Okayama, Japan
关键词:
Akt;
PKB;
glutathione transferase (GST);
glutathionylation;
MEK1;
2;
ML175;
S-GLUTATHIONYLATION;
OXIDATIVE STRESS;
PARKINSONS-DISEASE;
KINASES STRUCTURE;
REDOX REGULATION;
MOUSE MODEL;
PROTEIN;
APOPTOSIS;
ACTIVATION;
IDENTIFICATION;
D O I:
10.1002/prot.25683
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In the human neuroblastoma SH-SY5Y cell line, the glutathione transferase Omega 1-1 (GSTO1-1) appears to modulate Akt and MEK1/2 kinase activation. We observed a glutathionylation modification was involved in the activation of Akt but not MEK1/2. With the specific GSTO1-1 inhibitor ML175, we show the enzyme activity of GSTO1-1 is important for modulation as the inhibited GSTO1-1 allowed activation of both Akt and MEK1/2. The inhibition of GSTO1-1 showed a similar extent of activation of Akt and MEK1/2 as treatment by the endotoxin lipopolysaccharide. The GSTO1-1 also either directly interacts with Akt and MEK1/2 or interacts with a protein complexed with Akt and MEK1/2 as both kinases coimmunoprecipitated with GSTO1-1. The results suggest that GSTO1-1 enzyme activity inhibits the activation of these two kinases to maintain basal levels. The possible regulation by GSTO1-1 is of interest as both kinases have hundreds of potential downstream targets that are known to have contributions to various cellular processes including survival, growth, proliferation, and metabolism.
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页码:588 / 595
页数:8
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