Urbančič Vasja, Butler Richard, Richier Benjamin, Peter Manuel, Mason Julia, Livesey Frederick J, Holt Christine E, Gallop Jennifer L
Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, England, UK.
Department of Biochemistry, University of Cambridge, Cambridge, England, UK.
J Cell Biol. 2017 Oct 2;216(10):3405-3422. doi: 10.1083/jcb.201705113. Epub 2017 Jul 31.
Filopodia have important sensory and mechanical roles in motile cells. The recruitment of actin regulators, such as ENA/VASP proteins, to sites of protrusion underlies diverse molecular mechanisms of filopodia formation and extension. We developed Filopodyan (filopodia dynamics analysis) in Fiji and R to measure fluorescence in filopodia and at their tips and bases concurrently with their morphological and dynamic properties. Filopodyan supports high-throughput phenotype characterization as well as detailed interactive editing of filopodia reconstructions through an intuitive graphical user interface. Our highly customizable pipeline is widely applicable, capable of detecting filopodia in four different cell types in vitro and in vivo. We use Filopodyan to quantify the recruitment of ENA and VASP preceding filopodia formation in neuronal growth cones, and uncover a molecular heterogeneity whereby different filopodia display markedly different responses to changes in the accumulation of ENA and VASP fluorescence in their tips over time.
丝状伪足在运动细胞中具有重要的传感和机械作用。肌动蛋白调节因子(如ENA/VASP蛋白)募集到突起部位是丝状伪足形成和延伸的多种分子机制的基础。我们在斐济和R语言中开发了Filopodyan(丝状伪足动力学分析),以同时测量丝状伪足及其尖端和基部的荧光以及它们的形态和动态特性。Filopodyan支持高通量表型表征以及通过直观的图形用户界面进行丝状伪足重建的详细交互式编辑。我们高度可定制的流程具有广泛的适用性,能够在体外和体内检测四种不同细胞类型中的丝状伪足。我们使用Filopodyan来量化神经元生长锥中丝状伪足形成之前ENA和VASP的募集,并发现一种分子异质性,即不同的丝状伪足对其尖端ENA和VASP荧光积累随时间变化的反应明显不同。