F-actin capping (CapZ) and other contractile saphenous vein smooth muscle proteins are altered by hemodynamic stress - A proteomic approach

被引:58
作者
McGregor, E
Kempster, L
Wait, R
Gosling, M
Dunn, MJ
Powell, JT
机构
[1] Inst Psychiat, Proteome Sci PLC, S Wing Lab, Dept Neurosci, London SE5 8AF, England
[2] Charing Cross Hosp, Imperial Coll Sch Med, Dept Vasc Surg, London W6 8RP, England
[3] Univ London Imperial Coll Sci Technol & Med, Fac Med, Kennedy Inst Rheumatol Div, London W6 8LH, England
[4] Univ Hosp Coventry & Warwickshire, Coventry CV2 2DX, W Midlands, England
关键词
D O I
10.1074/mcp.M300046-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Increased force generation and smooth muscle remodeling follow the implantation of saphenous vein as an arterial bypass graft. Previously, we characterized and mapped 129 proteins in human saphenous vein medial smooth muscle using two-dimensional (2-D) PAGE and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Here, we focus on actin filament remodeling in response to simulated arterial flow. Human saphenous vein was exposed to simulated venous or arterial flow for 90 min in vitro, and the contractile medial smooth muscle was dissected out and subjected to 2-D gel electrophoresis using a non-linear immobilized pH 3-10 gradient in the first dimension. Proteins were analyzed quantitatively using PDQuest 2-D software. The actin polymerization inhibitor cytochalasin B (1 muM) prevented increases in force generation after 90 min of simulated arterial flow. At this time point, there were several consistent changes in actin filament-associated protein expression (seven paired vein samples). The heat shock protein HSP27, identified as a three-spot charge train, showed a 1.6-fold increase in abundance (p=0.01), but with reduced representation of the phosphorylated Ser(82) and Ser(15)Ser(82) isoforms (p=0.018). The abundance of actin-capping protein alpha2 subunit CapZ had decreased 3-fold, p=0.04. A 19-kDa proteolytic fragment of actin increased 2-fold, p=0.04. For the four-spot charge train of gelsolin, there was reduced representation of the more acidic isoforms, p=0.022. The abundance of other proteins associated with actin filaments, including cofilin and destrin, remained unchanged after arterial flow. Actin filament remodeling with differential expression and/or post-translational modification of proteins involved in capping the barbed end of actin filaments, HSP27 and CapZ, is an early response of contractile saphenous vein smooth muscle cells to hemodynamic stress. The observed changes would favor the generation of contractile stress fibers.
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页码:115 / 124
页数:10
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