Phosphorylation of ezrin on Thr567 is required for the synergistic activation of cell spreading by EPAC1 and protein kinase A in HEK293T cells

被引:17
作者
Parnell, Euan [1 ]
Koschinski, Andreas [2 ]
Zaccolo, Manuela [2 ]
Cameron, Ryan T. [3 ]
Baillie, George S. [3 ]
Baillie, Gemma L. [4 ]
Porter, Alison [4 ]
McElroy, Stuart P. [4 ]
Yarwood, Stephen J. [1 ]
机构
[1] Univ Glasgow, Inst Mol Cellular & Syst Biol, Coll Med Vet & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Oxford, Dept Physiol Anat & Genet, Oxford OX1 3QX, England
[3] Univ Glasgow, Coll Med Vet & Life Sci, Inst Cardiovasc & Med Sci, Glasgow G12 8QQ, Lanark, Scotland
[4] BioCity Scotland, European Screening Ctr, Newhouse ML1 5UH, Scotland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2015年 / 1853卷 / 07期
基金
英国生物技术与生命科学研究理事会;
关键词
Cyclic AMP; EPAC1; Cytoskeleton; Cell morphology; SIGNAL-REGULATED KINASE; EPIDERMAL-GROWTH-FACTOR; F-ACTIN BINDING; CYCLIC-AMP; BARRIER FUNCTION; EXCHANGE FACTOR; SOCS-3; GENE; CAMP; RAP1; INDUCTION;
D O I
10.1016/j.bbamcr.2015.04.009
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
Recent studies have demonstrated that the actin binding protein, ezrin, and the cAMP-sensor, EPAC1, cooperate to induce cell spreading in response to elevations in intracellular cAMP. To investigate the mechanisms underlying these effects we generated a model of EPAC1-dependent cell spreading based on the stable transfection of EPAC1 into HEK293T (HEK293T-EPAC1) cells. We found that direct activation of EPAC1 with the EPAC-selective analogue, 8-pCPT-2'-O-Me-cAMP (007), promoted cell spreading in these cells. In addition, co-activation of EPAC1 and PICA, with a combination of the adenylate cyclase activator, forskolin, and the cAMP phosphodiesterase inhibitor, rolipram, was found to synergistically enhance cell spreading, in association with cortical actin bundling and mobilisation of ezrin to the plasma membrane. PICA activation was also associated with phosphorylation of ezrin on Thr567, as detected by an electrophoretic band mobility shift during SDS-PAGE. Inhibition of PICA activity blocked ezrin phosphorylation and reduced the cell spreading response to cAMP elevation to levels induced by EPAC1-activation alone. Transfection of HEK293T-EPAC1 cells with inhibitory ezrin mutants lacking the key PICA phosphorylation site, ezrin-Thr567Ala, or the ability to associate with actin, ezrin-Arg579Ala, promoted cell arborisation and blocked the ability of EPAC1 and PICA to further promote cell spreading. The PICA phosphomimetic mutants of ezrin, ezrin-Thr567Asp had no effect on EPAC1-driven cell spreading. Our results indicate that association of ezrin with the actin cytoskeleton and phosphorylation on Thr567 are required, but not sufficient, for PICA and EPAC1 to synergistically promote cell spreading following elevations in intracellular CAMP. (C) 2015 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:1749 / 1758
页数:10
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