The pivotal role of protein kinase C zeta (PKCzeta) in insulin- and AMP-activated protein kinase (AMPK)-mediated glucose uptake in muscle cells

被引:18
作者
Liu, Li-Zhong [1 ]
Cheung, Stanley C. K. [1 ]
Lan, Lin-Lin [1 ]
Ho, Stanley K. S. [1 ]
Chan, Juliana C. N. [1 ]
Tong, Peter C. Y. [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong Inst Diabet & Obes, Prince Wales Hosp,Li Ka Shing Inst Hlth, Shatin, Hong Kong, Peoples R China
关键词
Signal integration; PKCzeta; AMPK; PKB; Insulin; Glucose homeostasis; SKELETAL-MUSCLE; GLUT4; TRANSLOCATION; RAT ADIPOCYTES; L6; MYOBLASTS; TRANSPORT; BERBERINE; AKT; ROSIGLITAZONE; MECHANISM; MYOTUBES;
D O I
10.1016/j.cellsig.2010.05.020
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Insulin and AMP-activated protein kinase (AMPK) signal pathways are involved in the regulation of glucose uptake. The integration of signals between these two pathways to maintain glucose homeostasis remains elusive. In this work, stimulation of insulin and berberine conferred a glucose uptake or surface glucose transporter 4 (GLUT4) translocation that was less than simple summation of their effects in insulin-sensitive muscle cells. Using specific inhibitors to key kinases of both pathways and PKCzeta small interference RNA, protein kinase C zeta (PKCzeta) was found to regulate insulin-stimulated protein kinase B (PKB) activation and inhibit AMPK activity on dorsal cell surface. In the presence of berberine, PKCzeta controlled AMPK activation and AMPK blocked PKB activity in perinuclear region. The inhibition effect of PKCzeta on AMPK activation or the arrestment of PKB activity by AMPK still existed in basal condition. These results suggest that there is antagonistic regulation between insulin and AMPK signal pathways, which is mediated by the switch roles of PKCzeta. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1513 / 1522
页数:10
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