Neutrophils Establish Rapid and Robust WAVE Complex Polarity in an Actin-Dependent Fashion

Autor: Orion D. Weiner, Sheel N. Dandekar, Andrew R. Houk, Arthur Millius
Jazyk: angličtina
Předmět:
Polarity (physics)
Neutrophils
Blotting
Western

macromolecular substances
Biology
Cell Fractionation
General Biochemistry
Genetics and Molecular Biology

Article
Quantitative Biology::Cell Behavior
Cell Line
Quantitative Biology::Subcellular Processes
03 medical and health sciences
Mice
Micromanipulation
0302 clinical medicine
Cell polarity
Animals
Actin
030304 developmental biology
0303 health sciences
Microscopy
Video

Agricultural and Biological Sciences(all)
Biochemistry
Genetics and Molecular Biology(all)

Dynamics (mechanics)
Cell Polarity
Chemotaxis
Polarization (waves)
Bridged Bicyclo Compounds
Heterocyclic

Actins
Cell biology
Wiskott-Aldrich Syndrome Protein Family
Multiprotein Complexes
Thiazolidines
CELLBIO
General Agricultural and Biological Sciences
WAVE complex
030217 neurology & neurosurgery
Intracellular
Zdroj: Current Biology. (3):253-259
ISSN: 0960-9822
DOI: 10.1016/j.cub.2008.12.044
Popis: Asymmetric intracellular signals enable cells to migrate in response to external cues. The multiprotein WAVE (SCAR/WASF) complex activates the actin-nucleating Arp2/3 complex [1-4] and localizes to propagating “waves”, which direct actin assembly during neutrophil migration [5, 6]. Here, we observe similar WAVE complex dynamics in other mammalian cells and analyze WAVE complex dynamics during the establishment of neutrophil polarity. Earlier models proposed that either spatially-biased generation [7] or selection of protrusions [8] enables chemotaxis. These models require existing morphological polarity to control protrusions. Similar spatially-biased generation and selection of WAVE complex recruitment occur in morphologically unpolarized neutrophils during the development of their first protrusions. Additionally, several mechanisms limit WAVE complex recruitment during polarization and movement: intrinsic cues restrict WAVE complex distribution during the establishment of polarity, and asymmetric intracellular signals constrain WAVE complex distribution in morphologically polarized cells. External gradients can overcome both intrinsic biases and control WAVE complex localization. Following latrunculin-mediated inhibition of actin polymerization, addition and removal of agonist gradients globally recruits and releases the WAVE complex from the membrane. Under these conditions the WAVE complex no longer polarizes, despite the presence of strong external gradients. Thus, actin polymer and the WAVE complex reciprocally interact during polarization.
Databáze: OpenAIRE