Myosin X and its motorless isoform differentially modulate dendritic spine development by regulating trafficking and retention of vasodilator-stimulated phosphoprotein

J Cell Sci. 2013 Oct 15;126(Pt 20):4756-68. doi: 10.1242/jcs.132969. Epub 2013 Aug 13.

Abstract

Myosin X (Myo10) is an unconventional myosin with two known isoforms: full-length (FL)-Myo10 that has motor activity, and a recently identified brain-expressed isoform, headless (Hdl)-Myo10, which lacks most of the motor domain. FL-Myo10 is involved in the regulation of filopodia formation in non-neuronal cells; however, the biological function of Hdl-Myo10 remains largely unknown. Here, we show that FL- and Hdl-Myo10 have important, but distinct, roles in the development of dendritic spines and synapses in hippocampal neurons. FL-Myo10 induces formation of dendritic filopodia and modulates filopodia dynamics by trafficking the actin-binding protein vasodilator-stimulated phosphoprotein (VASP) to the tips of filopodia. By contrast, Hdl-Myo10 acts on dendritic spines to enhance spine and synaptic density as well as spine head expansion by increasing the retention of VASP in spines. Thus, this study demonstrates a novel biological function for Hdl-Myo10 and an important new role for both Myo10 isoforms in the development of dendritic spines and synapses.

Keywords: Dendritic spine; Filopodia; Hippocampal neuron; Myosin; Synapse.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Cell Differentiation / physiology
  • Dendritic Spines / metabolism*
  • Dendritic Spines / physiology
  • HEK293 Cells
  • Hippocampus / metabolism
  • Humans
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism*
  • Myosins / genetics
  • Myosins / metabolism*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Protein Isoforms
  • Protein Transport
  • Pseudopodia / metabolism
  • Rats
  • Synapses / metabolism
  • Transfection

Substances

  • Cell Adhesion Molecules
  • MYO10 protein, human
  • Microfilament Proteins
  • Phosphoproteins
  • Protein Isoforms
  • vasodilator-stimulated phosphoprotein
  • Myosins