Triggering actin comets versus membrane ruffles: distinctive effects of phosphoinositides on actin reorganization

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Tasuku Ueno - , Johns Hopkins Medicine (Author)
  • Björn H Falkenburger - , University of Washington, RWTH Aachen University (Author)
  • Christopher Pohlmeyer - (Author)
  • Takanari Inoue - (Author)

Abstract

A limited set of phosphoinositide membrane lipids regulate diverse cellular functions including proliferation, differentiation, and migration. We developed two techniques based on rapamycin-induced protein dimerization to rapidly change the concentration of plasma membrane phosphatidylinositol 4,5-bisphosphate [PI(4,5)P(2)]. First, using a membrane-recruitable form of PI(4)P 5-kinase, we increased PI(4,5)P(2) synthesis from phosphatidylinositol 4-phosphate [PI(4)P] and found that COS-7, HeLa, and human embryonic kidney 293 cells formed bundles of motile actin filaments known as actin comets. In contrast, a second technique that increased the concentration of PI(4,5)P(2) without consuming PI(4)P induced membrane ruffles. These distinct phenotypes were mediated by dynamin-mediated vesicular trafficking and mutually inhibitory crosstalk between the small guanosine triphosphatases Rac and RhoA. Our results indicate that the effect of PI(4,5)P(2) on actin reorganization depends on the abundance of other phosphoinositides, such as PI(4)P. Thus, combinatorial regulation of phosphoinositide concentrations may contribute to the diversity of phosphoinositide functions.

Details

Original languageEnglish
Article numberra87
JournalScience signaling
Volume4
Issue number203
Publication statusPublished - 13 Dec 2011
Peer-reviewedYes
Externally publishedYes

External IDs

PubMedCentral PMC3372792
Scopus 83655193404
ORCID /0000-0002-2387-526X/work/176343380

Keywords

Keywords

  • Actins/chemistry, Animals, COS Cells, Cell Differentiation, Cell Membrane/metabolism, Cell Movement, Chlorocebus aethiops, HEK293 Cells, HeLa Cells, Humans, Mice, Microscopy, Confocal/methods, NIH 3T3 Cells, Phosphatidylinositol 4,5-Diphosphate/metabolism, Phosphatidylinositols/chemistry, Protein Structure, Tertiary, rho GTP-Binding Proteins/metabolism