Auxin transport inhibitors impair vesicle motility and actin cytoskeleton dynamics in diverse eukaryotes

Pankaj Dhonukshe(Netherlands Institute for Neuroscience), Ilya Grigoriev(Erasmus University Rotterdam), Rainer Fischer(University of Tübingen), M. Tominaga(National Institute of Information and Communications Technology), David G. Robinson(Heidelberg University), Jir̆ı́ Hašek(Czech Academy of Sciences), Tomasz Paciorek(University of Tübingen), Jan Petrášek(Czech Academy of Sciences, Institute of Experimental Botany), Daniela Seifertová(Czech Academy of Sciences, Institute of Experimental Botany), Ricardo Tejos(Universidad Andrés Bello), Lee A. Meisel(Universidad Andrés Bello), Eva Zažı́malová(Czech Academy of Sciences, Institute of Experimental Botany), Theodorus W. J. Gadella(Netherlands Institute for Neuroscience), York-Dieter Stierhof(University of Tübingen), Takashi Ueda(Tokyo University of Science), Kazuhiro Oiwa(National Institute of Information and Communications Technology), Anna Akhmanova(Erasmus University Rotterdam), Roland Brock(University of Tübingen), Anne Spang(Max Planck Society), Jiřı́ Friml(Masaryk University)
Proceedings of the National Academy of Sciences
March 12, 2008
Cited by 243Open Access
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Abstract

Many aspects of plant development, including patterning and tropisms, are largely dependent on the asymmetric distribution of the plant signaling molecule auxin. Auxin transport inhibitors (ATIs), which interfere with directional auxin transport, have been essential tools in formulating this concept. However, despite the use of ATIs in plant research for many decades, the mechanism of ATI action has remained largely elusive. Using real-time live-cell microscopy, we show here that prominent ATIs such as 2,3,5-triiodobenzoic acid (TIBA) and 2-(1-pyrenoyl) benzoic acid (PBA) inhibit vesicle trafficking in plant, yeast, and mammalian cells. Effects on micropinocytosis, rab5-labeled endosomal motility at the periphery of HeLa cells and on fibroblast mobility indicate that ATIs influence actin cytoskeleton. Visualization of actin cytoskeleton dynamics in plants, yeast, and mammalian cells show that ATIs stabilize actin. Conversely, stabilizing actin by chemical or genetic means interferes with endocytosis, vesicle motility, auxin transport, and plant development, including auxin transport-dependent processes. Our results show that a class of ATIs act as actin stabilizers and advocate that actin-dependent trafficking of auxin transport components participates in the mechanism of auxin transport. These studies also provide an example of how the common eukaryotic process of actin-based vesicle motility can fulfill a plant-specific physiological role.


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