Steering cell migration: lamellipodium dynamics and the regulation of directional persistence - PubMed (original) (raw)
Review
doi: 10.1038/nrm3861.
Affiliations
- PMID: 25145849
- DOI: 10.1038/nrm3861
Review
Steering cell migration: lamellipodium dynamics and the regulation of directional persistence
Matthias Krause et al. Nat Rev Mol Cell Biol. 2014 Sep.
Abstract
Membrane protrusions at the leading edge of cells, known as lamellipodia, drive cell migration in many normal and pathological situations. Lamellipodial protrusion is powered by actin polymerization, which is mediated by the actin-related protein 2/3 (ARP2/3)-induced nucleation of branched actin networks and the elongation of actin filaments. Recently, advances have been made in our understanding of positive and negative ARP2/3 regulators (such as the SCAR/WAVE (SCAR/WASP family verprolin-homologous protein) complex and Arpin, respectively) and of proteins that control actin branch stability (such as glial maturation factor (GMF)) or actin filament elongation (such as ENA/VASP proteins) in lamellipodium dynamics and cell migration. This Review highlights how the balance between actin filament branching and elongation, and between the positive and negative feedback loops that regulate these activities, determines lamellipodial persistence. Importantly, directional persistence, which results from lamellipodial persistence, emerges as a critical factor in steering cell migration.
References
- Cell Motil Cytoskeleton. 2006 Jan;63(1):6-13 -PubMed
- Nat Rev Mol Cell Biol. 2008 Nov;9(11):846-59 -PubMed
- J Cell Sci. 2012 Mar 1;125(Pt 5):1165-76 -PubMed
- Trends Cell Biol. 2010 Nov;20(11):650-61 -PubMed
- BMC Cell Biol. 2005 Mar 07;6(1):11 -PubMed
Publication types
MeSH terms
Substances
Grants and funding
- 077429/Z/05/Z/Wellcome Trust/United Kingdom
- 082907/Z/07/Z/Wellcome Trust/United Kingdom
- BB/F011431/1/Biotechnology and Biological Sciences Research Council/United Kingdom
- BB/G00319X/1/Biotechnology and Biological Sciences Research Council/United Kingdom
- BB/J000590/1/Biotechnology and Biological Sciences Research Council/United Kingdom
LinkOut - more resources
Full Text Sources
Other Literature Sources