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Synthetic polyamines promote rapid lamellipodial growth by regulating actin dynamics

机译:合成的多胺可通过调节肌动蛋白动力学来促进快速的片状脂质体生长

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Cellular protrusions involved in motile processes are driven by site-directed assembly of actin filaments in response to Rho-GTPase signalling. So far, only chemical compounds depolymerizing actin or stabilizing filaments, inhibiting N-WASP , Arp2/3 or formins, have been used to eliminate the formation of protrusions, while Rho-GTPase-dominant positive strategies have been designed to stimulate protrusions. Here we describe the design of four polyamines (macrocyclic and branched acyclic), and show that they enter the cell and induce specific growth of actin-enriched lamellipodia within minutes. The largest increase in cell area is obtained with micromolar amounts of a branched polyamine harbouring an 8-carbon chain. These polyamines specifically target actin both in vitro and in vivo . Analysis of their effects on filament assembly dynamics and its regulation indicates that the polyamines act by slowing down filament dynamics and by enhancing actin nucleation. These compounds provide new opportunities to study the actin cytoskeleton in motile and morphogenetic processes.
机译:响应于Rho-GTPase信号传导,肌动蛋白丝的定点组装驱动参与运动过程的细胞突起。迄今为止,仅使用解聚肌动蛋白或稳定细丝,抑制N-WASP,Arp2 / 3或formins的化合物来消除突起的形成,而Rho-GTPase主导的阳性策略已被设计用来刺激突起。在这里,我们描述了四种多胺(大环和支链无环)的设计,并显示它们进入细胞并在几分钟之内诱导富含肌动蛋白的片状脂质体的特异性生长。用微摩尔量的带有8碳链的支链多胺可以获得最大的细胞面积增加。这些多胺在体外和体内都专门针对肌动蛋白。分析它们对细丝装配动力学及其调节的影响,表明多胺通过减慢细丝动力学和增强肌动蛋白成核作用。这些化合物提供了研究运动和形态发生过程中肌动蛋白细胞骨架的新机会。

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