Podosome-regulating kinesin KIF1C translocates to the cell periphery in a CLASP-dependent manner

J Cell Sci. 2014 Dec 15;127(Pt 24):5179-88. doi: 10.1242/jcs.149633. Epub 2014 Oct 24.

Abstract

The kinesin KIF1C is known to regulate podosomes, actin-rich adhesion structures that remodel the extracellular matrix during physiological processes. Here, we show that KIF1C is a player in the podosome-inducing signaling cascade. Upon induction of podosome formation by protein kinase C (PKC), KIF1C translocation to the cell periphery intensifies and KIF1C accumulates both in the proximity of peripheral microtubules that show enrichment for the plus-tip-associated proteins CLASPs and around podosomes. Importantly, without CLASPs, both KIF1C trafficking and podosome formation are suppressed. Moreover, chimeric mitochondrially targeted CLASP2 recruits KIF1C, suggesting a transient CLASP-KIF1C association. We propose that CLASPs create preferred microtubule tracks for KIF1C to promote podosome induction downstream of PKC.

Keywords: CLASP; KIF1C; Kinesin; Microtubule; Podosome; Trafficking.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Surface Extensions / metabolism*
  • Humans
  • Kinesins / metabolism*
  • Microtubule-Associated Proteins / metabolism*
  • Microtubules / metabolism
  • Models, Biological
  • Muscle, Smooth, Vascular / cytology
  • Myocytes, Smooth Muscle / cytology
  • Myocytes, Smooth Muscle / metabolism
  • Protein Kinase C / metabolism
  • Protein Transport
  • Rats
  • Signal Transduction

Substances

  • CLASP1 protein, rat
  • CLASP2 protein, rat
  • KIF1C protein, human
  • Microtubule-Associated Proteins
  • Protein Kinase C
  • KIF1C protein, rat
  • Kinesins