Actin Filament Turnover Drives Leading Edge Growth during Myelin Sheath Formation in the Central Nervous System

• DOI: 10.1016/j.devcel.2015.05.013
• Publication Date: 2015-07-10T03:41:30Z
• Authors: Schanila Nawaz; Paula Sánchez; Sebastian Schmitt; Nicolas Snaidero; Mišo Mitkovski; Caroline Velte; Bastian R. Brückner; Ioannis Alexopoulos; Tim Czopka; Sang Y. Jung; Jeong S. Rhee; Andreas Janshoff; Walter Witke; Iwan A.T. Schaap; David A. Lyons; Mikael Simons
• Keywords: Central Nervous System; Cofilin 1; Mice, Knockout; 0303 health sciences; Patch-Clamp Techniques; Cell Membrane; Actins; Axons; 3. Good health; Mice, Inbred C57BL; Actin Cytoskeleton; Luminescent Proteins; Mice; Oligodendroglia; 03 medical and health sciences; Destrin; Cell Adhesion; Animals; Surface Tension; Cells, Cultured; Myelin Sheath; Zebrafish; Developmental Biology; Red Fluorescent Protein

During CNS development, oligodendrocytes wrap their plasma membrane around axons to generate multilamellar myelin sheaths. To drive growth at the leading edge of myelin at the interface with the axon, mechanical forces are necessary, but the underlying mechanisms are not known. Using an interdisciplinary approach that combines morphological, genetic, and biophysical analyses, we identified a key role for actin filament network turnover in myelin growth. At the onset of myelin biogenesis, F-actin is redistributed to the leading edge, where its polymerization-based forces push out non-adhesive and motile protrusions. F-actin disassembly converts protrusions into sheets by reducing surface tension and in turn inducing membrane spreading and adhesion. We identified the actin depolymerizing factor ADF/cofilin1, which mediates high F-actin turnover rates, as an essential factor in this process. We propose that F-actin turnover is the driving force in myelin wrapping by regulating repetitive cycles of leading edge protrusion and spreading.