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.
引用
收藏
页码:588 / 595
页数:8
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