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三元复合因子Net通过抑制PAI-1的表达来调节细胞迁移。

The ternary complex factor Net regulates cell migration through inhibition of PAI-1 expression.

作者信息

Buchwalter Gilles, Gross Christian, Wasylyk Bohdan

机构信息

Institut de Génétique et Biologie Moléculaire et Cellulaire, CNRS, INSERM, ULP, Illkirch, France.

出版信息

Mol Cell Biol. 2005 Dec;25(24):10853-62. doi: 10.1128/MCB.25.24.10853-10862.2005.

Abstract

Net, Elk-1, and Sap-1 are members of the ternary complex factor (TCF) subfamily of Ets transcription factors. They form ternary complexes with serum response factor (SRF) on serum response elements of immediate early genes such as c-fos and egr-1 and mediate responses to growth factors and mitogen-activated protein kinase signaling. Although the TCFs have been extensively studied as intermediates in signaling cascades, surprisingly little is known about their different target genes and physiological functions. We report that Net homozygous mutant mouse embryonic fibroblasts have a defect in cell migration. This defect results at least in part from increased expression of plasminogen activator inhibitor type 1 (PAI-1), a serine protease inhibitor (serpin) that controls extracellular proteolysis and cell matrix adhesion. The defect in cell migration can be reverted by the addition of a PAI-1 blocking antibody. Net represses PAI-1 promoter activity and binds to a specific region of the promoter containing Ets binding sites in the absence of SRF. We conclude that Net is a negative regulator of PAI-1 expression and is thereby involved in cell migration.

摘要

Net、Elk-1和Sap-1是Ets转录因子三元复合因子(TCF)亚家族的成员。它们与血清反应因子(SRF)在诸如c-fos和egr-1等立即早期基因的血清反应元件上形成三元复合物,并介导对生长因子和丝裂原活化蛋白激酶信号传导的反应。尽管TCFs作为信号级联反应的中间体已被广泛研究,但令人惊讶的是,关于它们不同的靶基因和生理功能却知之甚少。我们报告Net纯合突变小鼠胚胎成纤维细胞在细胞迁移方面存在缺陷。这种缺陷至少部分是由于纤溶酶原激活物抑制剂1型(PAI-1)表达增加所致,PAI-1是一种丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制剂家族),可控制细胞外蛋白水解和细胞与基质的黏附。添加PAI-1阻断抗体可逆转细胞迁移缺陷。在没有SRF的情况下,Net可抑制PAI-1启动子活性并与包含Ets结合位点的启动子特定区域结合。我们得出结论,Net是PAI-1表达的负调节因子,从而参与细胞迁移。

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