Shear stress modulates the expression of the atheroprotective protein Cx37 in endothelial cells

被引:67
作者
Pfenniger, Anna
Wong, Cindy
Sutter, Esther
Cuhlmann, Simon [2 ]
Dunoyer-Geindre, Sylvie [3 ]
Mach, Francois
Horrevoets, Anton J. [4 ]
Evans, Paul C. [2 ]
Krams, Rob [5 ]
Kwak, Brenda R. [1 ]
机构
[1] Univ Geneva, Dept Pathol & Immunol, Dept Internal Med Cardiol, Fdn Med Res, CH-1211 Geneva, Switzerland
[2] Univ London Imperial Coll Sci Technol & Med, BHF Cardiovasc Sci Unit, London, England
[3] Univ Geneva, Dept Internal Med Angiol & Hemostasis, CH-1211 Geneva, Switzerland
[4] Vrije Univ Amsterdam, Dept Mol Cell Biol & Immunol, Med Ctr, Amsterdam, Netherlands
[5] Univ London Imperial Coll Sci Technol & Med, Dept Bioengn, London, England
基金
瑞士国家科学基金会;
关键词
Cx37; Gap junction; Shear stress; KLF2; Endothelium; Gene expression; RAT AORTIC ENDOTHELIUM; KRUPPEL-LIKE FACTOR-2; TRANSCRIPTION FACTOR; GENE-EXPRESSION; DISTURBED FLOW; KLF2; ATHEROSCLEROSIS; GAP; CONNEXIN43; CHANNELS;
D O I
10.1016/j.yjmcc.2012.05.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
High laminar shear stress (HLSS) is vasculoprotective partly through induction of Kruppel-like factor 2 (KLF2). Connexin37 (Cx37) is highly expressed in endothelial cells (ECs) of healthy arteries, but not in ECs overlying atherosclerotic lesions. Moreover, Cx37 deletion in apolipoprotein E-deficient (ApoE(-/-)) mice increases susceptibility to atherosclerosis. We hypothesized that shear stress, through KLF2 modulation, may affect Cx37 expression in ECs. Cx37 expression and gap-junctional intercellular (GJIC) dye transfer are prominent in the straight portion of carotid arteries of ApoE(-/-) mice, but are reduced at the carotid bifurcation, a region subjected to oscillatory flow. Shear stress-modifying vascular casts were placed around the common carotid artery of ApoE(-/-) mice. Whereas Cx37 expression was conserved in HISS regions, it was downregulated to similar to 50% in low laminar or oscillatory flow regions. To study the mechanisms involved, HUVECs or bEnd.3 cells were exposed to flow in vitro. Cx37 and KLF2 expression were increased after 24 h of HISS. Interestingly, shear-dependent Cx37 expression was significantly reduced after silencing of KLF2. Moreover after exposure to simvastatin, a well-known KLF2 inducer, KLF2 binds to the Cx37 promoter region as shown by ChIP. Finally, GJIC dye transfer was highly reduced after KLF2 silencing and was increased after exposure to simvastatin. HLSS upregulates the expression of Cx37 in ECs by inducing its transcription factor KLF2, which increases intercellular communication. Therefore, this effect of shear stress on Cx37 expression may contribute to the synchronization of ECs and participate in the protective effect of HISS. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:299 / 309
页数:11
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