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Schelski, M.

Publications and source records attributed to Schelski, M..

2 recordsLinked to original sources

Slowdown of microtubule retrograde flow enables axon and dendrite development and maintenance

Distinct microtubule arrays form in axons and dendrites defining their functions in neurons. These arrays are thought to develop through separate processes. Here we challenge this view by showing that axons and dendrites develop by a unifying process: slowdown of microtubule retrograde flow (MT-RF), a recently discovered mechanism of microtubule dynamics. By integrating quantitative data of microtubule dynamics and distributions into a newly developed biophysical model of microtubules across developmental stages, we uncover that MT-RF interacts with microtubule stability and nucleation. Without MT-RF slowdown, this interaction suppresses development and maintenance of axonal and dendritic microtubule arrays. In axons, MT-RF slowdown enables microtubules to reach the tip, even at long distances, supporting axon growth. In dendrites, late MT-RF slowdown facilitates an efficient increase in stable microtubules. Thus, our data-integrated model reveals MT-RF slowdown as central for the development of distinct neuronal compartments, providing a unifying mechanism for microtubule-related physiology.

neuroscience↗

Microtubule retrograde flow retains neuronal polarization in a fluctuating state

In developing vertebrate neurons, a neurite is formed by more than a hundred microtubules. While individual microtubules are dynamic, the microtubule array itself has been regarded as stationary. Using live cell imaging in combination with photoconversion techniques and pharmacological manipulations, we uncovered that the microtubule array flows retrogradely within neurites to the soma. This microtubule retrograde flow drives cycles of microtubule density, a hallmark of the fluctuating state before axon formation. Shortly after axon formation, microtubule retrograde flow slows down in the axon, which stabilizes microtubule density cycles and thereby functions as a molecular wedge to enable axon extension. We propose microtubule retrograde flow and its specific slowdown in the axon to be the long-sought mechanism to single one neurite out to drive neuronal polarization.

neuroscience↗