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原肌球蛋白异构体的表达调节黏附的转变,以确定细胞的速度和方向。

Tropomyosin isoform expression regulates the transition of adhesions to determine cell speed and direction.

作者信息

Bach Cuc T T, Creed Sarah, Zhong Jessie, Mahmassani Maha, Schevzov Galina, Stehn Justine, Cowell Lauren N, Naumanen Perttu, Lappalainen Pekka, Gunning Peter W, O'Neill Geraldine M

机构信息

Oncology Research Unit, The Children's Hospital at Westmead, Westmead, New South Wales 2145, Australia.

出版信息

Mol Cell Biol. 2009 Mar;29(6):1506-14. doi: 10.1128/MCB.00857-08. Epub 2009 Jan 5.

Abstract

The balance of transition between distinct adhesion types contributes to the regulation of mesenchymal cell migration, and the characteristic association of adhesions with actin filaments led us to question the role of actin filament-associating proteins in the transition between adhesive states. Tropomyosin isoform association with actin filaments imparts distinct filament structures, and we have thus investigated the role for tropomyosins in determining the formation of distinct adhesion structures. Using combinations of overexpression, knockdown, and knockout approaches, we establish that Tm5NM1 preferentially stabilizes focal adhesions and drives the transition to fibrillar adhesions via stabilization of actin filaments. Moreover, our data suggest that the expression of Tm5NM1 is a critical determinant of paxillin phosphorylation, a signaling event that is necessary for focal adhesion disassembly. Thus, we propose that Tm5NM1 can regulate the feedback loop between focal adhesion disassembly and focal complex formation at the leading edge that is required for productive and directed cell movement.

摘要

不同黏附类型之间转变的平衡有助于间充质细胞迁移的调控,并且黏附与肌动蛋白丝的特征性关联促使我们质疑肌动蛋白丝相关蛋白在黏附状态转变中的作用。原肌球蛋白同工型与肌动蛋白丝的结合赋予了不同的丝结构,因此我们研究了原肌球蛋白在决定不同黏附结构形成中的作用。通过过表达、敲低和敲除方法的组合,我们确定Tm5NM1优先稳定黏着斑,并通过稳定肌动蛋白丝驱动向纤维状黏附的转变。此外,我们的数据表明Tm5NM1的表达是桩蛋白磷酸化的关键决定因素,桩蛋白磷酸化是黏着斑解体所必需的信号事件。因此,我们提出Tm5NM1可以调节前沿黏着斑解体和黏着复合体形成之间的反馈回路,而这是高效定向细胞运动所必需的。

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