Abstract

Migration of olfactory ensheathing cells (OECs) is critical for development of olfactory system and essential for neural regeneration after OEC transplantation into nerve injury site. However, the molecular mechanisms underlying the regulation of directional migration of OECs remain unclear. In this study, we found that in migrating OECs, phosphorylated myosin light chain (p-MLC, active myosin II) displayed a polarized distribution, with the leading front exhibiting higher than soma and trailing process. Over-expression of GFP-MLC significantly reduced OEC migration. Moreover, decreasing this front-to-rear difference of myosin II activity by the frontal application of a ML-7 (myosin II inhibitors) gradient induced the collapse of leading front and reversed soma translocation of OECs, whereas, increasing this front-to-rear difference of myosin II activity by the rear application of a ML-7 or BDM gradient or the frontal application of a Caly (myosin II activator) gradient accelerated the soma translocation of OECs. Finally, myosin II as a downstream signaling of repulsive factor Slit-2 mediated the reversal of soma translocation induced by Slit-2. Taken together, these results suggest that the polarized distribution of active myosin II regulates the directional migration of OECs during spontaneous migration or upon to extracellular stimulation such as Slit-2.

Highlights

  • Chain (MHC) dimers and two pairs of myosin light chains (MLCs)

  • We found that the polarized distribution of active myosin II regulates the directional migration of olfactory ensheathing cells (OECs) during spontaneous migration or upon to the repulsive factor Slit-2

  • To explore the potential effects of myosin II in OEC migration, we firstly examined the cellular distribution of active myosin II in cultured OECs

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Summary

Introduction

Chain (MHC) dimers and two pairs of myosin light chains (MLCs). Myosin II can bind reversibly to actin filaments, hydrolyze ATP in a process that is activated by actin and thereby convert chemical energy into mechanical force and movement. MLC20 is a substrate for a number of kinases, including Ca2+-calmodulin-dependent MLC kinase (MLCK)[24], Rho kinase and AMP-activated protein kinase (AMP kinase)[23, 25]. These kinases phosphorylate MLC20 primarily on Ser1926, which increases actin-activated MgATPase activity, filament formation and contractile activity in vitro and in vivo[21]. It remains unknown that whether NMII regulates the directional migration of OECs during spontaneous migration or upon to extracellular factor stimulation. We found that the polarized distribution of active myosin II regulates the directional migration of OECs during spontaneous migration or upon to the repulsive factor Slit-2

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