4.5 Article

XMAP215 promotes microtubule-F-actin interactions to regulate growth cone microtubules during axon guidance in Xenopus laevis

Journal

JOURNAL OF CELL SCIENCE
Volume 132, Issue 9, Pages -

Publisher

COMPANY BIOLOGISTS LTD
DOI: 10.1242/jcs.224311

Keywords

Growth cones; +TIP; Plus-end tracking proteins; CKAP5; Cytoskeleton; Super resolution; F-actin alignment

Categories

Funding

  1. National Institutes of Health [R00 MH095768, R01 MH109651]
  2. Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)

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It has long been established that neuronal growth cone navigation depends on changes in microtubule (MT) and F-actin architecture downstream of guidance cues. However, the mechanisms by which MTs and F-actin are dually coordinated remain a fundamentally unresolved question. Here, we report that the well-characterized MT polymerase, XMAP215 (also known as CKAP5), plays an important role in mediating MT-F-actin interaction within the growth cone. We demonstrate that XMAP215 regulates MT-F-actin alignment through its N-terminal TOG 1-5 domains. Additionally, we show that XMAP215 directly binds to F-actin in vitro and co-localizes with F-actin in the growth cone periphery. We also find that XMAP215 is required for regulation of growth cone morphology and response to the guidance cue, Ephrin A5. Our findings provide the first strong evidence that XMAP215 coordinates MT and F-actin interaction in vivo. We suggest a model in which XMAP215 regulates MT extension along F-actin bundles into the growth cone periphery and that these interactions may be important to control cytoskeletal dynamics downstream of guidance cues.

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