Dissection of keratin dynamics: different contributions of the actin and microtubule systems

Eur J Cell Biol. 2005 Mar;84(2-3):311-28. doi: 10.1016/j.ejcb.2004.12.004.

Abstract

It has only recently been recognized that intermediate filaments (IFs) and their assembly intermediates are highly motile cytoskeletal components with cell-type- and isotype-specific characteristics. To elucidate the cell-type-independent contribution of actin filaments and microtubules to these motile properties, fluorescent epithelial IF keratin polypeptides were introduced into non-epithelial, adrenal cortex-derived SW13 cells. Time-lapse fluorescence microscopy of stably transfected SW13 cell lines synthesizing fluorescent human keratin 8 and 18 chimeras HK8-CFP and HK18-YFP revealed extended filament networks that are entirely composed of transgene products and exhibit the same dynamic features as keratin systems in epithelial cells. Detailed analyses identified two distinct types of keratin motility: (I) Slow (approximately 0.23 microm/min), inward-directed, continuous transport of keratin filament precursor particles from the plasma membrane towards the cell interior, which is most pronounced in lamellipodia. (II) Fast (approximately 17 microm/min), bidirectional and intermittent transport of keratin particles in axonal-type cell processes. Disruption of actin filaments inhibited type I motility while type II motility remained. Conversely, microtubule disruption inhibited transport mode II while mode I continued. Combining the two treatments resulted in a complete block of keratin motility. We therefore conclude that keratin motility relies both on intact actin filaments and microtubules and is not dependent on epithelium-specific cellular factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / drug effects
  • Actin Cytoskeleton / metabolism
  • Actins / metabolism*
  • Antineoplastic Agents / pharmacology
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Genes, Reporter
  • Humans
  • Keratins / genetics
  • Keratins / metabolism*
  • Microscopy, Fluorescence
  • Microtubules / drug effects
  • Microtubules / metabolism*
  • Nocodazole / pharmacology
  • Protein Transport / drug effects
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Thiazoles / pharmacology
  • Thiazolidines

Substances

  • Actins
  • Antineoplastic Agents
  • Bridged Bicyclo Compounds, Heterocyclic
  • Recombinant Fusion Proteins
  • Thiazoles
  • Thiazolidines
  • Keratins
  • latrunculin B
  • Nocodazole